Bangalore Healthcare Jobs

Why This Role MattersThe Assistant Therapist role at The Association of People with Disability is essential in supporting children with developmental delays and disabilities. This role contributes directly to improving functional abilities, independence, and quality of life through guided therapeutic care and rehabilitation support.Job DescriptionThe Association of People with Disability is hiring an Assistant Therapist for a full-time, on-site role in Bangalore North. The role involves assisting physiotherapists in delivering therapy sessions, supporting rehabilitation programs, and working closely with children with special needs.Key Features of the Role• Position: Assistant Therapist• Organization: The Association of People with Disability• Location: Bangalore North• Employment Type: Full-time• Experience Required: 0–1 year• Salary: ₹15,000 per monthResponsibilities• Assist physiotherapists in conducting therapy sessions• Support implementation of individualized therapy plans• Help children perform exercises, mobility training, and functional activities• Prepare therapy materials and maintain equipment• Monitor children during sessions to ensure safety• Maintain therapy records, attendance, and progress notes• Support group therapy, early intervention, and rehabilitation programs• Guide caregivers on basic home exercises• Assist in screening, assessments, and therapy camps• Maintain cleanliness and organization of the therapy unitRequired Qualification• Diploma or Certificate in CCRT (Certificate Course in Rehabilitation Therapy) OR• Bachelor of Physiotherapy (BPT)Important Requirements• Basic knowledge of child development and disabilities• Understanding of physiotherapy exercises and rehabilitation techniques• Ability to work with children with conditions like cerebral palsy, autism, etc.• Good communication and interpersonal skills• Patience, empathy, and child-friendly approach• Ability to work in a multidisciplinary team• Basic documentation and record-keeping skillsEmployment Options• Full-time, on-site roleWhat We Offer• Opportunity to work in pediatric rehabilitation and early intervention• Exposure to multidisciplinary therapy environment• Hands-on experience with diverse therapy programs• Supportive and inclusive workplaceExperience and Skills• Experience in early intervention programs preferred• Ability to demonstrate therapy exercises• Basic computer skills for documentation• Strong teamwork and communication skillsSalary Insights• ₹15,000 per monthCompany OverviewThe Association of People with Disability is a leading non-profit organization dedicated to empowering people with disabilities through rehabilitation, education, and livelihood programs. The organization focuses on inclusive development and improving lives through multidisciplinary care.FAQsIs experience mandatory?No, freshers with relevant qualifications can apply.What type of patients will I work with?Children with developmental delays and disabilities.Is this a clinical role?It is a supportive clinical role assisting physiotherapists.What qualifications are required?CCRT certification or BPT degree.Is this a team-based role?Yes, you will work with therapists, educators, and other professionals.Application Tips• Highlight any experience with children or special needs care• Showcase empathy and communication skills• Include relevant certifications clearly• Emphasize willingness to learn and teamwork• Apply early to increase chances of selection

Why This Role MattersThe Manager – Physiotherapy Unit role at The Association of People with Disability is a leadership-driven position focused on delivering high-quality rehabilitation services. This role is critical in strengthening multidisciplinary care, improving patient outcomes, and mentoring future physiotherapy professionals while supporting both pediatric and adult rehabilitation programs.Job DescriptionThe Association of People with Disability is hiring a Manager – Physiotherapy Unit (Senior Physiotherapist) for its Bengaluru campus. This full-time, on-site leadership role involves advanced clinical service delivery, team supervision, and ensuring quality standards across physiotherapy and rehabilitation services.Key Features of the Role• Position: Manager – Physiotherapy Unit (Senior Physiotherapist)• Organization: The Association of People with Disability• Location: Bangalore North (Lingarajapuram Campus)• Employment Type: Full-time• Industry: NGO / Rehabilitation Services• Experience Required: 5–10 years• Salary: ₹7 LPA – ₹9 LPAResponsibilities• Conduct advanced physiotherapy assessments and develop goal-oriented treatment plans• Deliver evidence-based interventions focusing on mobility, strength, posture, and functional independence• Manage complex pediatric and outpatient rehabilitation cases• Monitor patient outcomes and modify treatment plans accordingly• Educate caregivers and families on therapy goals and home programs• Ensure ethical, safe, and patient-centered clinical practicesClinical Oversight & Quality Assurance• Supervise, mentor, and guide junior physiotherapists and therapy staff• Standardize assessment tools, therapy protocols, and documentation systems• Review treatment plans, reports, and outcome measures for quality and accuracy• Participate in multidisciplinary case discussions and care planning• Identify gaps and implement quality improvement initiativesOutpatient, Outreach & Rehabilitation Services• Oversee outpatient physiotherapy service delivery and scheduling• Support triage and continuity of care across departments• Contribute to outreach programs, camps, and community-based rehabilitation• Collaborate with multidisciplinary teams for integrated careDocumentation, Reporting & Systems• Ensure accurate and timely clinical documentation and reporting• Maintain standardized assessment records and outcome tracking• Oversee data entry and updates in clinical systems (e.g., Goonjan)• Contribute to audits, reports, and program evaluations• Ensure compliance with data protection and documentation policiesProfessional Leadership & Development• Participate in training programs and institutional initiatives• Mentor team members and support capacity building• Stay updated with latest physiotherapy practices and research• Demonstrate leadership, accountability, and teamworkRequired Qualification• Bachelor of Physiotherapy (BPT) with minimum 5 years of experience OR• Master of Physiotherapy (MPT) with minimum 2 years of experienceImportant Requirements• Experience in pediatric, neuro, or multidisciplinary rehabilitation preferred• Prior experience in supervision or mentoring is an advantage• Willingness to work with both pediatric and adult patients• Willingness to travel for outreach camps as requiredEmployment Options• Full-time, on-site roleWhat We Offer• Competitive salary package (₹7–₹9 LPA)• Opportunity to lead and shape rehabilitation services• Exposure to multidisciplinary and community-based care• Professional growth in a reputed NGO environment• Collaborative and purpose-driven workplaceExperience and Skills• Strong clinical expertise in physiotherapy assessment and treatment• Leadership and team management abilities• Knowledge of multidisciplinary rehabilitation models• Excellent communication and documentation skills• Proficiency in digital systems and reporting• Compassionate, ethical, and patient-focused approachSalary Insights• ₹7 LPA – ₹9 LPA (as per experience and organizational standards)Company OverviewThe Association of People with Disability is a leading non-profit organization dedicated to empowering people with disabilities through education, rehabilitation, and livelihood initiatives. With a strong focus on inclusive development, APD delivers comprehensive multidisciplinary rehabilitation services across India.FAQsIs this a leadership role?Yes, it involves managing the physiotherapy unit and mentoring staff.What type of patients will be handled?Both pediatric and adult patients in rehabilitation settings.Is travel required?Yes, for outreach programs and rehabilitation camps.What experience is preferred?Experience in pediatric, neuro, or multidisciplinary rehabilitation.What is the salary range?₹7 LPA to ₹9 LPA.Application Tips• Highlight leadership and team management experience• Showcase expertise in rehabilitation and physiotherapy protocols• Emphasize experience in pediatric or multidisciplinary settings• Include examples of clinical outcomes and quality improvement work• Demonstrate ability to handle both clinical and administrative responsibilities

Why This Role MattersResearch Associates play a vital role in pharmaceutical and biotechnology R&D by supporting drug discovery and development processes. Their work in chemical synthesis, analytical testing, and experimental documentation helps accelerate innovation and bring new therapies to market faster. This role is especially important in early-stage research, where precision, data integrity, and collaboration directly influence the success of scientific programs.Job DescriptionSyngene International Ltd. is hiring a Research Associate in Bangalore, India, within its Discovery and Development Services (DDS) division. This role focuses on synthetic chemistry and laboratory-based research activities, supporting drug discovery projects. The selected candidate will be involved in chemical synthesis, purification, analytical testing, and documentation while adhering to strict quality and safety standards. This is an excellent opportunity for MSc Chemical Sciences graduates looking to build a career in pharmaceutical R&D and gain hands-on experience in a global research environment.Key Features of the Role: Responsibilities• Perform synthetic chemistry reactions and related laboratory processes.• Conduct reaction workups and purify compounds using techniques such as column chromatography, crystallization, recrystallization, and preparative TLC.• Operate laboratory instruments and ensure proper usage.• Submit synthesized samples for analysis and record results accurately.• Maintain detailed experimental records in lab notebooks or electronic systems.• Communicate progress and findings to supervisors and team members.• Ensure proper packaging and shipment of samples.• Maintain and calibrate laboratory instruments; report breakdowns promptly.• Follow Material Safety Data Sheet (MSDS) guidelines and safety procedures.• Ensure proper waste segregation and compliance with EHS norms.• Prepare and update SOPs, IOPs, EOPs, and OCPs as required.• Participate in training programs and maintain updated training records.• Adhere to data integrity, confidentiality, and quality standards.• Support independent or team-based research projects, including immuno-oncology programs.• Conduct experiments, analyze data, and prepare study reports.• Collaborate with cross-functional research teams and mentor junior scientists when required.Eligibility CriteriaEducational Qualification• M.Sc in Chemical SciencesExperience• Freshers or candidates with relevant laboratory experience can applyRequired Skills• Strong understanding of chemical synthesis concepts• Hands-on experience with laboratory techniques and instruments• Knowledge of analytical techniques and data interpretation• Familiarity with chromatography and purification methods• Good documentation and record-keeping skills• Strong communication and teamwork abilitiesBehavioral Skills• Good presentation and communication skills• Hardworking, sincere, and detail-oriented• Strong sense of responsibility and accountability• Ability to work collaboratively in a team environmentSalary Insights• Competitive salary as per industry standards (entry to mid-level R&D role)Benefits & Perks• Opportunity to work with global pharmaceutical and biotech clients• Exposure to advanced drug discovery and development projects• Hands-on training in synthetic chemistry and lab techniques• Career growth in research and development• Collaborative and innovation-driven work environmentCompany OverviewSyngene International Ltd., established in 1993, is a leading global contract research, development, and manufacturing organization (CRDMO). The company provides integrated scientific services across pharmaceuticals, biotechnology, nutrition, animal health, and specialty chemicals. With a strong client base including global leaders, Syngene is known for its innovation-driven culture and commitment to scientific excellence. Its team of scientists works collaboratively to solve complex research challenges, improve R&D productivity, and accelerate time-to-market for innovative solutions.FAQs• Is this role suitable for freshers?Yes, MSc graduates with relevant knowledge can apply.• What is the main focus of this role?Synthetic chemistry, laboratory research, and drug discovery support.• Are safety protocols important in this role?Yes, strict adherence to EHS and safety guidelines is mandatory.Application Tips• Highlight your academic projects related to chemical synthesis• Mention hands-on experience with lab techniques and instruments• Include knowledge of analytical methods and data interpretation• Emphasize teamwork, documentation, and safety awareness

Why This Role MattersClinical Data Programmers play a key role in ensuring the accuracy, integrity, and compliance of clinical trial data. Their work directly supports drug development, regulatory submissions, and patient safety by maintaining high-quality clinical datasets. This role is especially important in bridging clinical research and data analytics within global trials.Job DescriptionNovotech is hiring a Clinical Data Programmer I (SAS) in Bangalore, India. The role involves supporting clinical trial data programming, validation, and reporting while ensuring compliance with Good Clinical Data Management Practices (GCDMP). This is an excellent opportunity for professionals interested in clinical data management and SAS programming within a global CRO environment.Key Features of the Role: Responsibilities• Develop and maintain SAS programs for clinical data management.• Perform data cleaning, validation, and discrepancy management.• Generate clinical data listings, reports, and extracts.• Ensure compliance with GCDMP and regulatory standards.• Assist in database validation and quality checks.• Collaborate with clinical data managers, statisticians, and project teams.• Maintain programming documentation and standards.• Support database lock activities and data integrity checks.Eligibility CriteriaEducational Qualification• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biostatistics, Computer Science, or related field.Experience• Freshers or candidates with relevant experience can apply.Required Skills• Knowledge of SAS programming in clinical trials.• Understanding of clinical data management processes.• Familiarity with GCDMP and clinical trial standards.• Strong analytical and data validation skills.• Good communication and teamwork abilities.Preferred Skills• Knowledge of CDISC standards (SDTM / ADaM).• Experience with clinical databases or EDC systems.• Exposure to clinical trial data programming and reporting.Salary Insights• ₹6,00,000 – ₹9,00,000 per annum (approx.)Benefits & Perks• Exposure to global clinical trials.• Health and wellness benefits.• Professional training and certification support.• Career growth opportunities within a global CRO.Company OverviewNovotech is a leading global Contract Research Organization (CRO) specializing in clinical development and regulatory services. With a strong presence in the Asia-Pacific region, Novotech supports pharmaceutical and biotech companies in conducting efficient and compliant clinical trials worldwide.FAQs• Is SAS knowledge mandatory?Yes, basic knowledge of SAS programming is required.• Is this role suitable for freshers?Yes, candidates with relevant skills and knowledge can apply.• What is the focus of the role?Clinical data programming, validation, and compliance in clinical trials.Application Tips• Highlight your SAS programming skills and projects.• Mention knowledge of clinical data standards (GCDMP, CDISC).• Include any internship or coursework related to clinical trials.• Emphasize analytical and data handling skills.

Why This Role MattersThe Consultant General Surgeon role at Svayou Healthcare is crucial for delivering high-quality surgical care and ensuring safe, effective treatment outcomes. This role directly impacts patient recovery and supports advanced clinical services in a modern healthcare setup.Job DescriptionSvayou Healthcare is hiring a Consultant General Surgeon for a part-time, on-site role in Bangalore Urban. The role involves performing surgical procedures, managing patient care, and collaborating with medical teams.Key Features of the Role• Position: Consultant General Surgeon• Organization: Svayou Healthcare• Location: Bangalore Urban• Employment Type: Part-time• Work Mode: On-site• Selection Mode: InterviewResponsibilities• Diagnose and treat surgical conditions• Perform general surgical procedures with precision• Provide pre-operative and post-operative care• Maintain detailed patient records and documentation• Collaborate with multidisciplinary healthcare teams• Ensure adherence to safety and medical protocolsRequired Qualification• MS in General Surgery from a recognized institution• Valid medical license to practice in IndiaImportant Requirements• Strong diagnostic and analytical skills• Expertise in modern surgical techniques• Excellent communication and teamwork abilities• Commitment to ethical and professional standardsEmployment Options• Part-time consultant role• On-site clinical practiceWhat We Offer• Flexible working opportunity• Exposure to diverse surgical cases• Modern healthcare environment• Collaborative and supportive teamExperience and Skills• Proven experience in general surgery• Surgical precision and patient care expertise• Ability to manage complex cases• Strong interpersonal and communication skillsSalary Insights• Not disclosed (competitive as per industry standards)Company OverviewSvayou Healthcare is a comprehensive healthcare provider offering diagnostics, rehabilitation, home care, and specialized medical services through a patient-centric and digital-first approach.FAQsWhat is the qualification required?MS in General Surgery with a valid medical license.Is this a full-time role?No, it is a part-time role.What is the work location?Bangalore Urban, Karnataka.What skills are required?Surgical expertise, patient care, teamwork, and communication.Is salary mentioned?No, salary details are not disclosed.Application Tips• Highlight surgical experience and case exposure• Mention specific procedures you have performed• Keep your medical registration details ready• Prepare for clinical and scenario-based discussions• Apply early through the job link

Why This Role MattersThe Consultant Dermatologist role at Svayou Healthcare is essential for delivering specialized skin care and enhancing patient confidence through expert diagnosis and treatment. This role contributes to high-quality dermatological care in a modern, digital-first healthcare environment.Job DescriptionSvayou Healthcare is hiring a Consultant Dermatologist for a part-time, on-site role in Bangalore Urban. The role focuses on diagnosing and treating skin, hair, and nail conditions while also offering cosmetic dermatology services.Key Features of the Role• Position: Consultant Dermatologist• Organization: Svayou Healthcare• Location: Bangalore Urban• Employment Type: Part-time• Work Mode: On-site• Selection Mode: InterviewResponsibilities• Diagnose and treat skin, hair, and nail conditions• Provide consultations and personalized skincare plans• Perform cosmetic dermatology procedures• Manage conditions such as acne and related disorders• Educate patients on skincare and treatment options• Maintain patient records and ensure quality careRequired Qualification• MD/DNB in Dermatology or equivalent• Valid registration with Medical Council of India or State CouncilImportant Requirements• Expertise in dermatology and cosmetology• Strong diagnostic and treatment skills• Excellent communication and patient-handling abilities• Ability to stay updated with latest dermatological advancementsEmployment Options• Part-time role• On-site clinical practiceWhat We Offer• Flexible part-time opportunity• Exposure to modern, digital-first healthcare systems• Opportunity to perform advanced cosmetic procedures• Collaborative work environmentExperience and Skills• Clinical experience in dermatology• Proficiency in cosmetic dermatology procedures• Strong patient interaction and consultation skills• Attention to detail and precision in treatmentsSalary Insights• Salary not disclosed (competitive as per industry standards)Company OverviewSvayou Healthcare is a comprehensive healthcare provider offering medical specialties, diagnostics, rehabilitation, and home care services with a strong focus on digital innovation and patient-centered care.FAQsWhat is the qualification required?MD/DNB in Dermatology or equivalent.Is this a full-time role?No, it is a part-time role.What is the work location?Bangalore Urban, Karnataka.What skills are required?Dermatology expertise, cosmetology skills, and strong communication.Is salary mentioned?No, salary details are not disclosed.Application Tips• Highlight dermatology and cosmetology experience in your CV• Mention procedures you are skilled in (lasers, peels, etc.)• Keep your medical registration details ready• Prepare for practical and case-based discussions• Apply early through the job link

Why This Role MattersMedical Representatives play a crucial role in the pharmaceutical industry by acting as the link between pharmaceutical companies and healthcare professionals. Their primary responsibility is to communicate scientific information about medicines to doctors and pharmacists, helping them make informed prescribing decisions that support patient care. Through regular engagement with healthcare professionals, medical representatives help increase awareness of pharmaceutical products and support responsible prescription practices. Their work contributes to improved patient access to medicines while also helping pharmaceutical companies strengthen their presence in competitive healthcare markets. This position provides an excellent opportunity for science and pharmacy graduates to begin a career in pharmaceutical sales, healthcare marketing, and field-based roles while developing strong communication and relationship-building skills.Job DescriptionThe Medical Representative will be responsible for promoting pharmaceutical products to doctors, pharmacists, and other healthcare professionals within the assigned territory. The role focuses on generating prescriptions through effective field visits, product demonstrations, and professional relationship development with healthcare providers. Employees in this role are expected to conduct regular visits to healthcare professionals to present pharmaceutical products and communicate their therapeutic benefits according to company guidelines. Representatives must perform structured pre-call planning before each doctor visit to prepare objectives and ensure effective communication during the interaction. The role also involves conducting Retail Chemist Prescription Audit to monitor prescription patterns, evaluate competitor activity, and identify opportunities for product growth in the assigned territory. These insights help medical representatives develop effective promotional strategies and strengthen market presence. In addition to doctor engagement, representatives coordinate with chemists and distribution partners to ensure that pharmaceutical products are available at pharmacies when prescriptions are generated. Maintaining product availability helps ensure that patients receive their prescribed medicines without delays. Medical representatives also play an important role in supporting the launch of new pharmaceutical products by implementing marketing strategies designed by the company and communicating product benefits to healthcare professionals.Key Features of the Role: Responsibilities• Conduct regular field visits to healthcare professionals to promote pharmaceutical products.• Generate prescriptions by presenting scientific product information to doctors and pharmacists.• Perform structured pre-call planning before each doctor visit.• Conduct Retail Chemist Prescription Audit to analyze prescription trends and competitor activity.• Maintain accurate records of doctor visits and field activities in company systems.• Build and maintain strong professional relationships with healthcare professionals.• Ensure regular engagement with prescribers to prevent prescriber loss in the territory.• Support the successful launch of new pharmaceutical products.• Maintain and update doctor and chemist lists according to company guidelines.• Coordinate with chemists and distribution partners to ensure product availability.• Generate product order bookings according to company sales targets.• Manage distribution partners such as stockists in the assigned territory.Required Qualifications• Bachelor of Science (BSc)• Bachelor of Pharmacy (B.Pharm)• Diploma in Pharmacy (D.Pharm)• Master of Business Administration (MBA)Experience and Skills• Freshers and candidates with up to four years of experience can apply.• Basic scientific knowledge related to pharmaceutical products and therapies.• Strong communication and interpersonal skills.• Ability to build professional relationships with healthcare professionals.• Good presentation and persuasion abilities.• Ability to manage field-based work and achieve sales targets.Technical Skills• Ability to maintain field reports and documentation of doctor visits.• Familiarity with digital sales reporting tools and mobile reporting systems.• Basic proficiency in communication and documentation tools.Preferred Skills• Strong product presentation and demonstration skills.• Ability to analyze market trends and competitor activity.• Effective territory planning and time management skills.• Customer relationship management abilities.• Self-motivated and results-driven approach.Additional Requirements• Candidate must possess a valid two-wheeler driving license.• Ownership of a two-wheeler vehicle is mandatory for field travel.• Willingness to travel frequently within the assigned territory.• Flexibility to relocate anywhere in India if required.Salary InsightsMedical representative roles generally offer a fixed salary along with performance-based incentives, travel allowances, and additional benefits depending on company policies.Company OverviewAlembic Pharmaceuticals Limited is a well-established pharmaceutical company in India known for its strong presence in branded formulations, generics, and active pharmaceutical ingredients. The company operates globally approved manufacturing facilities and supplies pharmaceutical products to both domestic and international markets. With a strong focus on research, innovation, and quality manufacturing, the organization continues to expand its therapeutic portfolio and strengthen its presence in global pharmaceutical markets.FAQs• What does a Medical Representative do?Medical representatives promote pharmaceutical products to doctors and pharmacists and help generate prescriptions through scientific communication.• Can fresh graduates apply for this role?Yes. Freshers and candidates with up to four years of experience are eligible.• Is this a field-based role?Yes. The position requires frequent travel to meet doctors and pharmacies within the assigned territory.Application Tips• Highlight communication and interpersonal skills in your resume.• Mention academic knowledge related to pharmacy, science, or healthcare.• Emphasize willingness to travel and work in field sales roles.• Demonstrate interest in pharmaceutical marketing and healthcare engagement.

Why This Role MattersPharmacovigilance is essential for ensuring the safety and effectiveness of medicines throughout their lifecycle. From clinical trials to post-marketing surveillance, pharmacovigilance professionals monitor adverse events, analyze safety data, and ensure that pharmaceutical products comply with global regulatory requirements. The Pharmacovigilance Associate role at Alvotech plays a key part in supporting global safety data management for biosimilar medicines. The position contributes to the monitoring of safety data generated from clinical trials and post-marketing programs while maintaining compliance with international pharmacovigilance regulations.Working within the Global Safety Data Management team, the PV Associate will assist in managing adverse event reports, monitoring safety signals, and supporting pharmacovigilance system operations. This role also contributes to improving pharmacovigilance processes and ensuring regulatory compliance across global safety programs. For professionals with pharmacovigilance experience, this role offers valuable exposure to global drug safety operations, safety databases, and regulatory frameworks governing biosimilar medicines.Job DescriptionAlvotech is seeking a motivated Pharmacovigilance Associate to support clinical safety and post-marketing pharmacovigilance activities within its Research and Development function. The selected candidate will be part of the Global Safety Data Management team and will contribute to safety data handling, regulatory reporting, and pharmacovigilance process development. The role involves working with safety databases, managing adverse event cases, and ensuring that safety information is processed in accordance with international regulatory requirements.The PV Associate will collaborate with multiple internal departments and external partners to ensure timely safety reporting and regulatory compliance across global clinical and post-marketing programs.Key Features of the Role• Opportunity to work within global pharmacovigilance and safety data management• Exposure to clinical trial safety monitoring and post-marketing surveillance• Involvement in pharmacovigilance system configuration and lifecycle management• Collaboration with global regulatory, quality, and clinical teams• Participation in safety process improvement and compliance initiatives• Opportunity to support safety monitoring for biosimilar medicinesResponsibilitiesClinical Safety & Pharmacovigilance Activities• Support assigned clinical safety and post-marketing pharmacovigilance activities• Manage Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) processing• Assist in regulatory safety submissions and reporting requirements• Perform literature monitoring and digital platform monitoring for safety signals• Conduct pharmacovigilance reconciliations and safety data verification• Support activities related to EudraVigilance and XEVMPDSafety Systems & Data Management• Assist in configuration, validation, and lifecycle management of pharmacovigilance systems• Maintain safety databases and ensure accurate safety data management• Work with safety systems such as Oracle Argus Safety, ARISg Safety System, and Veeva Vault SafetyPharmacovigilance Process Support• Assist in maintaining and optimizing global pharmacovigilance procedures• Ensure compliance with internal SOPs and international safety regulations• Support safety documentation and regulatory compliance activitiesCross-Functional Collaboration• Work with pharmacovigilance teams involved in benefit-risk management and clinical trials• Collaborate with departments such as Quality, Regulatory Affairs, IT, and Clinical Program Development• Coordinate with external pharmacovigilance service providers and business partnersTraining, Audits & Compliance• Support pharmacovigilance training for internal staff and external stakeholders• Assist in safety-related audits and regulatory inspections• Maintain accurate documentation to meet global regulatory requirementsRequired QualificationsEducational Requirements• Master’s degree in Pharmaceutical Sciences, Pharmacy, Medicine, or Life SciencesExperience and Skills• Minimum 2 years of experience in Pharmacovigilance or Drug Safety• Experience working in safety data management functions• Hands-on experience in clinical trial safety and post-marketing pharmacovigilance• Familiarity with pharmacovigilance safety databases• Experience working with global pharmaceutical products and clinical trials• Knowledge of biologic or combination products is considered an advantageRegulatory Knowledge• Understanding of global pharmacovigilance regulations including• ICH Guidelines• FDA Regulations• Good Pharmacovigilance Practices• Good Clinical Practice• Council for International Organizations of Medical Sciences safety reporting standardsProfessional Skills• Strong organizational and time-management skills• Excellent written and verbal communication abilities• Ability to manage multiple safety activities and meet deadlines• Capability to work independently and collaboratively in multicultural teamsSalary InsightsAlthough the exact salary has not been specified, Pharmacovigilance Associate roles in the global biopharmaceutical industry typically offer competitive compensation based on experience, location, and expertise. Employees may also receive additional benefits such as professional development opportunities, global project exposure, and involvement in innovative biosimilar research programs.Company OverviewAlvotech is a global biopharmaceutical company focused on developing and manufacturing high-quality biosimilar medicines.The company specializes in improving access to biologic treatments by producing cost-effective biosimilars while maintaining strict regulatory, safety, and quality standards. Within its Research and Development division, the Integrated Clinical and Medical Research department develops strategies aligned with global biosimilar guidelines and regulatory authority requirements to support successful clinical studies and post-marketing safety programs.Through advanced pharmacovigilance systems and global safety monitoring processes, Alvotech ensures that its biosimilar medicines meet international safety and regulatory standards.FAQsWho can apply for this role?Candidates with a Master’s degree in Pharmacy, Life Sciences, or Medicine and at least 2 years of pharmacovigilance experience.What type of work does the PV Associate perform?The role involves adverse event case processing, safety monitoring, regulatory reporting, safety database management, and pharmacovigilance compliance activities.Is experience with safety databases required?Yes. Experience with systems such as Argus, ARISg, or Veeva Vault Safety is preferred.Does the role involve working with clinical trials?Yes. The position supports safety monitoring for both clinical trials and post-marketing pharmacovigilance programs.Application Tips• Highlight your pharmacovigilance experience and safety data management expertise• Include experience working with ICSR processing and SAE reporting• Mention knowledge of safety databases such as Argus or Veeva Vault Safety• Demonstrate familiarity with global PV regulations such as ICH, GVP, and GCP guidelines• Emphasize strong documentation practices and attention to detail

Why This Role MattersThe Senior Associate – Data Sciences in Global Market Vigilance plays a key role in monitoring product safety and post-market surveillance data across global markets. The position focuses on safety analytics, signal detection, and regulatory compliance to ensure that adverse event trends are identified early and managed effectively, supporting consumer safety and regulatory requirements.Job DescriptionUnilever is hiring a Senior Associate – Data Sciences within the Global Market Vigilance (GMV) team at its R&D center in Bengaluru. The role focuses on pharmacovigilance data analytics, adverse event case management, and signal detection activities while ensuring compliance with global regulatory standards and maintaining inspection readiness.Key Features of the Role• Opportunity to work in global pharmacovigilance and safety data analytics• Exposure to post-market surveillance and safety monitoring processes• Hands-on work with safety databases and advanced analytics tools• Collaboration with regulatory affairs, R&D, and quality teams• Involvement in global adverse event trending and signal detection activitiesResponsibilitiesCase Management and Compliance• Lead or perform adverse event intake, triage, and documentation using safety systems such as Veeva Vault Safety• Conduct duplicate checks and ensure high-quality safety data for analysis• Perform seriousness, causality, and expectedness assessments with proper documentation• Ensure compliance with MedDRA coding standards, SOPs, and global adverse event reporting requirementsSafety Data Analytics, Trending and Signal Detection• Perform quantitative and qualitative safety data analysis across brands and markets• Develop dashboards, KPIs, and safety scorecards for monitoring trends• Conduct global adverse event trending, signal detection, and safety pattern analysis• Validate potential safety signals through case series evaluation and confounder assessments• Support automation initiatives across the pharmacovigilance lifecycleSystem and Process Optimization• Support configuration, testing, and validation of pharmacovigilance safety databases• Perform safety data audits, reconciliation, and root cause investigations• Implement process improvements to enhance data integrity and analytics readinessCross-Functional Collaboration and Leadership• Act as the analytics and safety contact for regulatory affairs, R&D, quality teams, and customer support groups• Present safety trends, risks, and signals to stakeholders and governance forums• Mentor junior associates in pharmacovigilance analytics and documentation standards• Drive corrective and preventive actions related to safety data issuesRequired QualificationsEducational Requirements• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related fieldExperience and Skills• 5–8 years of experience in pharmacovigilance, safety analytics, or global market vigilance• Hands-on experience with pharmacovigilance systems such as Veeva Vault Safety or similar platforms• Strong knowledge of safety data trending, signal detection, and pharmacovigilance analytics• Experience with analytics tools such as Power BI, Tableau, SQL, or advanced Excel• Familiarity with automation or AI-enabled pharmacovigilance workflows• Strong understanding of audit readiness, quality management systems, and vendor oversight]Salary InsightsSalary details were not specified in the job posting and are expected to be offered as per company standards and experience.Company OverviewUnilever is a global consumer goods company known for its wide portfolio of health, beauty, and wellbeing products. The company invests heavily in research and development to ensure product safety, quality, and regulatory compliance across international markets.FAQs• What qualification is required for this role?Candidates should have a bachelor’s or master’s degree in life sciences, pharmacy, or a related discipline.• How much experience is required?Applicants should have approximately 5–8 years of experience in pharmacovigilance, safety analytics, or post-market surveillance.• Where is the job located?The role is based at the Unilever R&D center in Bengaluru, Karnataka.• What type of work will the candidate perform?The role involves pharmacovigilance data analytics, adverse event case management, signal detection, and safety trend monitoring.Application Tips• Highlight experience in pharmacovigilance systems and safety data analysis• Mention knowledge of MedDRA coding and adverse event processing• Include experience with analytics tools such as Power BI, Tableau, or SQL• Showcase expertise in signal detection and pharmacovigilance compliance• Demonstrate strong documentation and regulatory compliance skills

Why This Role MattersClinical trials generate large volumes of complex data that must be accurately collected, managed, and analyzed to support regulatory submissions and scientific decision-making. Clinical Data Management plays a critical role in ensuring that this data is reliable, consistent, and compliant with regulatory standards. The Associate Manager – Clinical Data Management supports the successful execution of clinical research projects by overseeing data management activities throughout the clinical trial lifecycle. This includes designing data collection systems, managing clinical databases, and ensuring that clinical trial data meets strict quality and regulatory requirements. In modern clinical research, data quality is essential for maintaining the integrity of study results and ensuring patient safety. Data management professionals ensure that clinical data is accurate, complete, and ready for statistical analysis and regulatory review.Another important aspect of the role involves collaboration with cross-functional teams such as clinical operations, biostatistics, and external vendors. By coordinating data management activities across these groups, the Associate Manager helps ensure that clinical trial milestones are achieved efficiently. The role also involves implementing data standards, maintaining documentation, and supporting regulatory inspections or audits. Strong oversight of external vendors and contract research organizations is essential to ensure that all deliverables meet quality expectations and project timelines. For professionals experienced in clinical data management, this position provides an opportunity to lead data-related activities within global clinical trials while contributing to the development of high-quality healthcare products. Overall, the role supports the successful management of clinical trial data, enabling pharmaceutical and healthcare companies to generate reliable evidence for regulatory approvals and product development.Job DescriptionThe Associate Manager – Clinical Data Management is responsible for planning, coordinating, and overseeing data management activities related to clinical research projects. The role ensures that clinical trial data is collected, processed, and maintained in compliance with regulatory guidelines and organizational standards. Professionals in this role manage the design and implementation of data management tasks for clinical studies, including the development of electronic data capture systems and data management plans. They collaborate closely with clinical and biostatistics teams to ensure that study data meets the requirements for statistical analysis and regulatory submissions. The position also involves managing data collection systems such as Electronic Data Capture (EDC) platforms and integrating data from external systems including electronic patient-reported outcomes and other clinical data sources. In addition to technical responsibilities, the Associate Manager provides oversight of external vendors responsible for data management services. This includes evaluating vendor proposals, monitoring service delivery, and ensuring compliance with service-level agreements. The role also includes reviewing study documentation, organizing data quality review meetings, and ensuring that clinical datasets remain accurate and complete throughout the study lifecycle. Overall, the position combines leadership, data management expertise, and cross-functional collaboration to ensure the successful delivery of high-quality clinical trial data.Key Features of the Role:• Leadership role within clinical data management operations.• Opportunity to manage end-to-end clinical trial data processes.• Collaboration with clinical operations, biostatistics, and regulatory teams.• Involvement in data quality management and regulatory compliance.• Exposure to advanced clinical data systems and digital data collection tools.• Opportunity to oversee external vendors and CRO partners.• Participation in global clinical research projects.• Career development in clinical data management and clinical research leadership.Responsibilities• Plan and manage data management activities for clinical research projects.• Design and implement data management solutions for complex clinical studies.• Ensure all data management activities comply with regulatory guidelines and quality standards.• Coordinate with clinical and biostatistics teams to support clinical data analysis.• Manage electronic data capture systems and other clinical data collection platforms.• Author and review data management study documents including Data Management Plans and eCRF guidelines.• Conduct data quality review meetings with cross-functional study teams.• Monitor and ensure data accuracy, completeness, and consistency throughout clinical trials.• Provide oversight to external vendors and contract research organizations responsible for data management deliverables.• Evaluate proposals from external service providers and manage vendor relationships.• Maintain clinical data standards and support the development of standardized data structures.• Support regulatory inspections and audits related to clinical data management.• Mentor junior team members and support their professional development.Required Qualifications• Strong understanding of clinical data management processes.• Knowledge of clinical trial regulations and industry standards.• Ability to manage complex projects and coordinate cross-functional teams.• Strong analytical and problem-solving skills.• Excellent communication and stakeholder management abilities.Educational Requirements• Bachelor’s degree in Mathematics, Science, Pharmacy, Life Sciences, or a related field.Experience and Skills• Minimum of 8 years of clinical data management experience in the healthcare or pharmaceutical industry.• Strong knowledge of clinical trial regulations including International Council for Harmonisation guidelines and Good Clinical Practice standards.• Experience working with Clinical Data Management Systems (CDMS) and Electronic Data Capture platforms.• Experience integrating data from multiple clinical data sources such as eCOA and external datasets.• Strong project management and organizational skills.• Experience managing vendor relationships and service delivery agreements.• Ability to analyze clinical data metrics and generate reports for decision-making.• Strong written and verbal communication skills.Salary InsightsAssociate Manager – Clinical Data Management roles in India typically offer salaries ranging from ₹18 LPA to ₹28 LPA, depending on experience, leadership responsibilities, and expertise in clinical data systems.Company OverviewKenvue is a global consumer health company known for its trusted healthcare brands and commitment to science-driven innovation. The organization develops and markets well-known healthcare and personal care products including Neutrogena, Aveeno, Tylenol, Listerine, Johnson's, and Band-Aid.With a strong heritage in consumer healthcare and a focus on science-based innovation, the company operates globally and serves millions of consumers through its health and wellness products.FAQs• What does a Clinical Data Management Associate Manager do?This role oversees the management of clinical trial data, ensuring data accuracy, quality, and compliance with regulatory standards.• What systems are commonly used in clinical data management?Professionals typically work with Electronic Data Capture systems and Clinical Data Management Systems.• Is vendor management part of this role?Yes, the role includes oversight of external vendors and CRO partners responsible for data management deliverables.• What career growth opportunities exist?Professionals may advance to roles such as Clinical Data Management Manager, Director of Data Management, or Head of Clinical Data Operations.Application Tips• Highlight experience in clinical data management systems and electronic data capture platforms.• Emphasize knowledge of regulatory standards such as ICH guidelines and Good Clinical Practice.• Showcase experience coordinating cross-functional clinical research teams.• Demonstrate experience managing vendor relationships and project timelines.• Include examples of clinical studies or data management projects you have supported.

Why This Role MattersData-driven insights are becoming increasingly important in the healthcare and medical technology industries. Organizations rely on healthcare data analytics to understand market trends, evaluate product performance, and make informed strategic decisions. The role of an Associate Healthcare Research & Data Analyst supports these objectives by analyzing healthcare datasets and generating insights that help companies navigate complex MedTech markets.Medical device companies and healthcare organizations depend on accurate data and market intelligence to understand customer demand, identify growth opportunities, and remain competitive in global markets. Analysts working in this domain play a vital role in interpreting large datasets and transforming them into actionable insights. The position also contributes to market research initiatives that evaluate industry trends, product positioning, and competitive landscapes. Through primary and secondary research, analysts help organizations understand the evolving needs of healthcare providers, patients, and regulatory environments. Another key aspect of the role involves maintaining and improving healthcare datasets used for forecasting and market modeling. Ensuring data quality and accuracy is critical for generating reliable insights and supporting business decision-making. For graduates from pharmacy, biotechnology, life sciences, or medical technology backgrounds, this role offers a unique opportunity to combine scientific knowledge with data analytics and market research skills. It also provides exposure to global healthcare markets and consulting projects within the MedTech sector. Overall, the Associate Healthcare Research & Data Analyst contributes to building data-driven healthcare intelligence that supports innovation, strategic planning, and improved healthcare solutions worldwide.Job DescriptionThe Associate Healthcare Research & Data Analyst works within the healthcare analytics and market research team to analyze data related to medical devices and healthcare markets. The role involves collecting, organizing, and interpreting healthcare datasets to generate insights that support market analysis and strategic decision-making. Professionals in this role work closely with data analysts, product managers, and subject matter experts to maintain healthcare databases and develop analytical models that track market performance and product trends. The position requires conducting both primary and secondary market research to gather information about healthcare technologies, medical device markets, and competitive landscapes. Analysts use this information to support forecasting models and provide strategic insights to clients and internal teams. Another important responsibility involves maintaining product catalogs and healthcare datasets used for market intelligence platforms. Analysts identify inconsistencies in data and ensure that information remains accurate, complete, and up to date. The role also includes preparing analytical reports and presentations that communicate insights to stakeholders, including consulting teams, clients, and senior management. Overall, the position combines healthcare research, data analytics, and market intelligence to support informed decision-making within the medical technology industry.Key Features of the Role:• Entry-level opportunity in healthcare data analytics and MedTech market research.• Exposure to global medical device and healthcare markets.• Opportunity to work with large real-world healthcare datasets.• Involvement in market research and competitive intelligence projects.• Collaboration with international healthcare analytics and consulting teams.• Opportunity to develop skills in data analysis, forecasting, and market modelling.• Hybrid work environment supporting professional development and collaboration.• Career growth opportunities in healthcare analytics and consulting.Responsibilities• Analyze healthcare and medical device datasets to generate market insights.• Conduct primary and secondary research related to healthcare and MedTech markets.• Perform competitive intelligence analysis for medical device companies.• Build and maintain datasets used for forecasting and market modeling.• Design and analyze surveys related to healthcare products and markets.• Maintain product catalog and SKU databases for medical device markets.• Identify trends, patterns, and strategic insights from healthcare data.• Resolve data inconsistencies and improve data quality within healthcare datasets.• Prepare analytical reports and presentations for internal teams and clients.• Collaborate with product managers, subject matter experts, and consulting teams.• Support the development of healthcare analytics products and platforms.Required Qualifications• Strong analytical and data interpretation skills.• Ability to work with large datasets and generate meaningful insights.• Strong communication and presentation skills.• Ability to manage multiple projects and meet deadlines.Educational Requirements• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)• B.E in Biotechnology or Medical Electronics• M.Sc in Biotechnology or Life Sciences• Other related healthcare or science degreesExperience and Skills• Freshers or candidates with up to 6 months of experience can apply.• Knowledge of SQL or Python for data analysis is desirable.• Strong proficiency in Microsoft Excel for data analysis and reporting.• Understanding of healthcare datasets and market research methodologies.• Ability to analyze large datasets and identify trends and patterns.• Strong written and verbal communication skills.• Ability to collaborate effectively within cross-functional teams.• Good organizational skills and attention to detail.Salary InsightsEntry-level healthcare research and data analyst roles in India typically depending on educational background, technical skills, and analytical expertise. Candidates with strong data analysis skills such as SQL, Python, or advanced Excel may receive higher compensation packages.Company OverviewClarivate is a global provider of trusted insights and analytics that help organizations accelerate innovation. The company supports industries including life sciences, healthcare, academia, and intellectual property through advanced data analytics, research platforms, and consulting services. Within its healthcare division, Clarivate provides market intelligence and analytics solutions to pharmaceutical and medical device companies, enabling them to make strategic decisions based on reliable data and industry insights.FAQs• What does a Healthcare Research & Data Analyst do?A Healthcare Research & Data Analyst analyzes healthcare datasets, conducts market research, and generates insights for medical device and healthcare companies.• Is programming knowledge required for this role?Basic knowledge of SQL or Python is beneficial but may not always be mandatory for entry-level roles.• What industries does this role support?The role primarily supports medical device companies, healthcare organizations, and life sciences businesses.• What career growth opportunities exist?Professionals may advance to roles such as Senior Healthcare Analyst, Healthcare Data Scientist, or Healthcare Consulting Specialist.Application Tips• Highlight analytical skills and experience working with datasets.• Emphasize proficiency in Microsoft Excel, SQL, or Python.• Showcase any academic or internship experience in healthcare research or market analysis.• Demonstrate strong communication and presentation abilities.• Include examples of data analysis projects or research work in your resume.

Why This Role MattersPharmacovigilance professionals play an essential role in safeguarding patient health by monitoring the safety of medicines and ensuring timely reporting of adverse events. Accurate safety data collection, evaluation, and reporting are crucial to maintaining regulatory compliance and protecting patients worldwide.The Japan Local Case Advisor role at AstraZeneca is particularly important because it focuses on managing safety reports related to products used in the Japanese market. The position supports Individual Case Safety Report processing, adverse event reporting, and compliance with Japanese pharmacovigilance regulations.Working within the Global Business Services Patient Safety team, the role involves collaborating with global safety teams while ensuring that local Japanese regulatory requirements are met. This includes managing safety cases, performing data entry into safety databases, and supporting pharmacovigilance compliance activities. For professionals with pharmacovigilance experience and Japanese language proficiency, this role provides a unique opportunity to contribute to global drug safety programs while supporting patient safety initiatives for important therapeutic products.Job DescriptionAstraZeneca is seeking a Japan Local Case Advisor to support pharmacovigilance operations within the Global Business Services Patient Safety function.The selected candidate will be responsible for managing Individual Case Safety Reports and supporting safety reporting activities related to AstraZeneca and Rare Disease Unit products in Japan. The role requires proficiency in English and Japanese and involves collaboration with internal safety teams to ensure timely and accurate safety data processing. This position involves case intake activities, safety database data entry, regulatory compliance monitoring, and support for audits and inspections. The role also contributes to maintaining pharmacovigilance quality systems and ensuring adherence to Japanese regulatory standards.Key Features of the RoleOpportunity to work in global pharmacovigilance and patient safety operationsExposure to safety reporting for the Japanese pharmaceutical marketInvolvement in Individual Case Safety Report management and adverse event reportingCollaboration with multinational teams in a global pharmaceutical environmentParticipation in pharmacovigilance quality systems and compliance activitiesOpportunity to contribute to safety monitoring for innovative medicinesResponsibilitiesCase Intake and Safety ReportingAccept and validate safety reports for domestic cases in Japan and conduct preliminary case assessments. Communicate with reporters when necessary to collect additional safety information and ensure the accuracy of safety reports. Ensure proper handling of personal and confidential information in accordance with regulatory requirements and company policies. Perform routine quality checks and initiate follow-up activities when additional information is required. Collaborate with internal teams to clarify case details, triage incoming safety reports, and escalate urgent or reportable cases for further investigation.Safety Data Entry and Case ManagementEnter safety data accurately into pharmacovigilance databases and ensure that all relevant information is documented correctly. Work with internal teams to resolve data entry issues and ensure high-quality safety documentation. Initiate follow-up requests using product or event-specific questionnaires to obtain additional safety information when required.Audit and Inspection SupportMaintain pharmacovigilance documentation in accordance with internal procedures and regulatory requirements. Support internal and external audits and assist with regulatory authority inspections by ensuring inspection-ready documentation.Regulatory ComplianceEnsure compliance with Japanese regulatory standards for Individual Case Safety Reports and adverse event reporting. Identify urgent or high-risk cases and escalate them according to established safety procedures.Quality Management System SupportContribute to the effective implementation of the pharmacovigilance Quality Management System and maintain awareness of regulatory changes related to the Japanese pharmaceutical market.General ResponsibilitiesPerform peer reviews of safety cases and support additional pharmacovigilance projects when required. Collaborate with internal teams on pharmacovigilance aspects related to organized data collection programs.Required QualificationsEducational RequirementsBachelor’s degree in Life Sciences, Pharmacy, Medicine, or a related scientific field.Experience and Skills1 to 2 years of experience working with safety databases or pharmacovigilance data entry. Strong attention to detail and the ability to identify sensitive personal or confidential information in safety reports. Experience working collaboratively with cross-functional teams and the ability to resolve operational issues effectively.Language RequirementsJapanese language proficiency at N2 level or higher for listening, writing, and speaking. Reading proficiency in Japanese medical terminology and Kanji characters at N3 to N1 level. English language proficiency equivalent to A2 level according to the CEFR framework.Technical KnowledgeFamiliarity with pharmacovigilance processes and adverse event reporting standards. Experience with safety databases such as Oracle Argus Safety is preferred. Knowledge of global pharmacovigilance guidelines such as Good Pharmacovigilance Practice and Good Clinical Practice is considered advantageous. Understanding of medical coding systems such as MedDRA and WHO Drug Dictionary is beneficial.Professional SkillsStrong problem-solving and analytical abilities. Excellent written and verbal communication skills. Ability to work effectively in multicultural teams and collaborate with stakeholders across different regions.Salary InsightsAlthough the exact salary package has not been disclosed, pharmacovigilance roles within global pharmaceutical companies typically offer competitive compensation based on experience, skills, and regional policies. Employees may also benefit from professional development opportunities, exposure to global pharmacovigilance operations, and participation in international patient safety initiatives.Company OverviewAstraZeneca is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines that transform patient care. The company operates across multiple therapeutic areas including oncology, cardiovascular diseases, respiratory conditions, and rare diseases. AstraZeneca places strong emphasis on patient safety and regulatory compliance, supported by advanced pharmacovigilance systems and global safety monitoring programs. Through collaborative research, advanced technology, and strong global partnerships, AstraZeneca continues to develop life-changing medicines while maintaining high standards of quality and safety.FAQsWho can apply for this role?Candidates with a life sciences background and pharmacovigilance experience, along with Japanese language proficiency.Is Japanese language proficiency mandatory?Yes. Japanese language skills at N2 level or higher are required for handling domestic safety cases in Japan.What type of work does the Japan Local Case Advisor perform?The role involves case intake, safety data entry, adverse event reporting, regulatory compliance monitoring, and audit support.Is experience with safety databases required?Experience with pharmacovigilance safety databases such as Argus is preferred.Application TipsHighlight your pharmacovigilance or safety data management experience in your resume.Mention your proficiency in Japanese language and experience working with Japanese regulatory requirements.Include experience with safety databases and adverse event reporting systems.Demonstrate your attention to detail and ability to handle confidential information responsibly.Showcase your ability to collaborate with global teams and manage safety case documentation accurately.

Why This Role MattersMedical data abstraction plays a crucial role in healthcare analytics, clinical research, and real-world evidence generation. Data abstractors review medical records and extract clinically relevant information to support research studies, healthcare analytics, and evidence-based medical insights.The Medical Data Abstractor role focuses on reviewing electronic medical records, identifying relevant clinical information, and entering structured data into electronic systems. By accurately extracting patient information such as diagnoses, treatments, adverse events, and medication details, professionals in this role contribute to high-quality healthcare data used in clinical research and healthcare decision-making.This position is particularly important in areas such as oncology, cardiovascular diseases, and metabolic disorders where detailed patient data is required for clinical analysis and research. For candidates with medical or healthcare backgrounds, the role offers an opportunity to work with real-world clinical data while contributing to healthcare analytics and research initiatives.Job DescriptionThe organization is seeking Medical Data Abstractors to support clinical data abstraction and medical record review activities at its Bangalore location.The selected candidate will navigate electronic medical record systems, review patient records, and extract relevant clinical data according to project-specific requirements. The role involves understanding medical reports, identifying relevant clinical information, and entering accurate data into designated electronic databases. Medical Data Abstractors will also collaborate with project teams, respond to queries from project leads, and contribute to continuous improvement of data abstraction processes.Key Features of the Role• Opportunity to work in medical data abstraction and healthcare analytics• Exposure to electronic medical record systems and clinical databases• Involvement in reviewing patient medical records and clinical documentation• Participation in healthcare data projects across multiple therapeutic areas• Collaboration with healthcare analytics and clinical research teams• Opportunity to develop expertise in real-world healthcare data analysisResponsibilitiesMedical Record Review• Access electronic medical record systems and other medical databases to review patient records• Identify and extract relevant medical information according to project-specific requirements• Understand diagnostic reports, pathology reports, and clinical documentation to obtain accurate dataClinical Data Abstraction• Enter extracted clinical data into designated electronic data systems• Categorize information related to inclusion and exclusion criteria, adverse events, hospitalizations, and medications• Ensure data accuracy and consistency during abstraction activitiesProject Familiarization and Knowledge Development• Review project-specific documentation to understand study objectives and abstraction requirements• Use available resources to build medical knowledge relevant to assigned projects• Stay updated with project procedures and abstraction guidelinesTeam Collaboration and Knowledge Sharing• Share medical knowledge and project-specific procedural information with other data abstractors• Participate in periodic team meetings and contribute to abstraction workflow discussions• Support team members with project-related queries when requiredQuery Resolution and Communication• Respond promptly to queries raised by lead abstractors, operations managers, or project teams• Clarify clinical data discrepancies when reviewing medical records• Ensure communication with project personnel regarding abstraction tasks and updatesAdditional Responsibilities• Assist in reviewing medical records to assess eligibility for new projects• Support ongoing improvements in data abstraction processes and workflowsRequired QualificationsEducational Requirements• BDS or MDS (Oral Pathology, Oral Medicine, or Public Health Dentistry)• B.Sc Nursing or M.Sc NursingExperience and Skills• 0 to 4 years of experience in medical record review, healthcare data abstraction, or clinical documentation analysis• Strong understanding of medical terminology and clinical documentation• Ability to interpret diagnostic reports, pathology reports, and patient treatment records• Knowledge of clinical concepts such as adverse events, medications, and hospitalization data• Experience reviewing medical records or patient treatment data is preferredPreferred Knowledge• Oncology experience or understanding of cancer diagnosis, treatment, and recovery processes• Familiarity with medical data related to therapeutic areas such as cardiovascular, immunology, and metabolic diseasesTechnical Skills• Strong computer skills and ability to work with electronic data systems• Familiarity with medical record databases and healthcare data platforms• Ability to learn and adapt to new software systems and digital toolsProfessional Skills• Strong critical thinking and analytical abilities• Excellent organizational and time-management skills• Ability to work independently and make informed decisions when abstracting data• Flexibility to adapt to changing project requirements and work schedulesSalary InsightsAlthough the exact salary is not specified, Medical Data Abstractor roles in healthcare analytics and clinical data services typically offer competitive compensation depending on experience, qualifications, and project complexity. Additional benefits may include exposure to healthcare data analytics projects, professional development opportunities, and experience working with real-world medical data.Company OverviewConcertAI is a healthcare analytics and data science company that leverages real-world medical data to support clinical research, healthcare decision-making, and drug development. The organization collaborates with healthcare providers, life sciences companies, and research institutions to generate valuable insights from clinical data. By combining advanced data analytics with medical expertise, ConcertAI helps improve healthcare outcomes, accelerate clinical research, and support evidence-based medical innovation.FAQsWho can apply for this role?Candidates with BDS, MDS (Oral Pathology, Oral Medicine, or Public Health Dentistry), B.Sc Nursing, or M.Sc Nursing qualifications.What experience is required for this position?Applicants with 0 to 4 years of experience in medical data review, clinical documentation analysis, or healthcare data abstraction can apply.What type of work will the Medical Data Abstractor perform?The role involves reviewing medical records, extracting clinical information, and entering structured data into electronic databases.Is oncology experience required?Oncology experience is preferred but not mandatory. Knowledge of other therapeutic areas such as cardiovascular or immunology is also considered.Are computer skills required for this role?Yes. Since most tasks involve reviewing electronic records and entering data into digital systems, strong computer skills are essential.Application Tips• Highlight experience reviewing medical records or clinical documentation• Mention knowledge of medical terminology and patient treatment data• Demonstrate ability to interpret diagnostic and pathology reports• Showcase experience working with electronic medical record systems or healthcare databases• Emphasize analytical skills and attention to detail when handling clinical data

Why This Role MattersPharmacovigilance is a critical function in the pharmaceutical and biopharmaceutical industry, ensuring that medicines remain safe and effective throughout their lifecycle. From clinical trials to post-marketing surveillance, pharmacovigilance professionals monitor adverse events, analyze safety data, and ensure regulatory compliance with international drug safety standards.The Senior Pharmacovigilance Specialist role at Alvotech is essential in maintaining the safety profile of biosimilar medicines and supporting global safety operations. The position focuses on safety data management for clinical trials and post-marketing programs while ensuring that pharmacovigilance activities meet international regulatory requirements. As part of the Global Safety Data Management team, the Senior PV Specialist will contribute to safety data analysis, adverse event reporting, regulatory submissions, and the development of pharmacovigilance processes and systems. The role also supports safety system lifecycle management and cross-functional collaboration with clinical, regulatory, and quality teams.This position provides experienced pharmacovigilance professionals with the opportunity to work on global drug safety programs while contributing to the development and monitoring of biosimilar medicines.Job DescriptionAlvotech is seeking a skilled Senior Pharmacovigilance Specialist to support clinical safety and post-marketing pharmacovigilance activities within its Research and Development function. The selected candidate will join the Global Safety Data Management team and will be responsible for managing safety data related to clinical trials and marketed products. The role involves overseeing adverse event reporting, maintaining safety databases, ensuring regulatory compliance, and supporting the development of pharmacovigilance systems and processes.The Senior PV Specialist will also collaborate with cross-functional teams across the organization to ensure that safety activities are performed efficiently and in compliance with global pharmacovigilance standards.Key Features of the Role• Opportunity to work in global pharmacovigilance and safety data management• Involvement in clinical trial safety monitoring and post-marketing surveillance• Participation in pharmacovigilance system configuration and lifecycle management• Collaboration with global regulatory, quality, and clinical teams• Contribution to safety process optimization and regulatory compliance initiatives• Exposure to safety monitoring for biosimilar medicinesResponsibilitiesClinical Safety & Pharmacovigilance Activities• Manage assigned clinical safety and post-marketing pharmacovigilance activities• Handle Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) processing• Support regulatory safety submissions and reporting requirements• Conduct literature monitoring and digital platform monitoring for safety signals• Perform pharmacovigilance reconciliations and safety data reviews• Support activities related to EudraVigilance and XEVMPDSafety Systems & Data Management• Participate in configuration, validation, and lifecycle management of pharmacovigilance systems• Maintain and monitor safety databases to ensure data accuracy and regulatory compliance• Work with safety systems such as Oracle Argus Safety, ARISg Safety System, and Veeva Vault SafetyPharmacovigilance Process Management• Create, maintain, and optimize global pharmacovigilance processes• Ensure compliance with international regulatory guidelines and company procedures• Monitor pharmacovigilance activities to maintain regulatory compliance across clinical and post-marketing programsCross-Functional Collaboration• Work closely with pharmacovigilance teams involved in benefit-risk management and clinical trials• Collaborate with departments such as Quality, Regulatory Affairs, IT, and Clinical Program Development• Coordinate with external pharmacovigilance service providers and business partnersTraining, Audits & Compliance• Deliver pharmacovigilance training programs to internal staff and external partners• Participate in safety-related audits and regulatory inspections• Ensure proper documentation and compliance with global pharmacovigilance standardsRequired QualificationsEducational Requirements• Master’s degree in Pharmaceutical Sciences, Pharmacy, Medicine, or Life SciencesExperience and Skills• Minimum 5 years of experience in Pharmacovigilance or Drug Safety• Strong experience in safety data management functions• Hands-on experience in clinical trial safety and post-marketing pharmacovigilance activities• Experience working with global pharmaceutical products and clinical trials• Familiarity with biologic or combination products is considered an advantageTechnical Knowledge• Experience working with pharmacovigilance safety systems such as Oracle Argus Safety, ARISg Safety System, or Veeva Vault Safety• Understanding of global pharmacovigilance regulations including• ICH Guidelines• FDA Regulations• Good Pharmacovigilance Practices• Good Clinical Practice• Council for International Organizations of Medical Sciences safety reporting standardsProfessional Skills• Strong analytical, organizational, and time-management skills• Excellent communication and stakeholder management abilities• Ability to work independently and manage complex pharmacovigilance activities• Comfortable working in global and multicultural teamsSalary InsightsAlthough the salary package has not been specified, Senior Pharmacovigilance Specialist roles in the global biopharmaceutical industry typically offer competitive compensation based on experience, expertise, and geographic location.Additional benefits may include international project exposure, professional development opportunities, and involvement in global clinical safety programs.Company OverviewAlvotech is a global specialty biopharmaceutical company dedicated to developing and manufacturing high-quality biosimilar medicines.The company focuses exclusively on biosimilars with the goal of improving access to biologic treatments while maintaining strict regulatory and quality standards. Within the Research and Development function, the Integrated Clinical and Medical Research department develops clinical strategies aligned with biosimilar regulatory guidelines and health authority requirements. Through advanced safety monitoring systems and global pharmacovigilance operations, Alvotech ensures the safety, effectiveness, and regulatory compliance of its products worldwide.FAQsWho can apply for this role?Candidates with a Master’s degree in Pharmacy, Life Sciences, or Medicine and at least 5 years of pharmacovigilance experience.What type of work does the Senior PV Specialist perform?The role includes adverse event management, safety data analysis, regulatory reporting, safety system management, and pharmacovigilance compliance activities.Is experience with safety databases required?Yes. Experience with systems such as Argus, ARISg, or Veeva Vault Safety is preferred.Does the role involve working with clinical trials?Yes. The position supports safety monitoring for both clinical trials and post-marketing pharmacovigilance programs.Application Tips• Highlight your pharmacovigilance and safety data management experience• Mention expertise in ICSR processing, SAE reporting, and regulatory submissions• Include knowledge of safety databases such as Argus or Veeva Vault Safety• Demonstrate familiarity with global PV regulations such as ICH, GVP, and GCP guidelines• Emphasize strong documentation practices and cross-functional collaboration skills

Why This Role MattersPharmacovigilance plays a critical role in ensuring the safety of medicines throughout their lifecycle, from clinical trials to post-marketing surveillance. Drug safety professionals monitor adverse events, analyze safety data, and ensure compliance with global regulatory standards to protect patient health.The Pharmacovigilance Specialist role at Alvotech provides an excellent opportunity to work in global safety data management within the biopharmaceutical industry. The position supports safety monitoring for clinical trials and post-marketing programs while ensuring adherence to international pharmacovigilance regulations. As part of the Global Safety Data Management team, the specialist will contribute to safety systems, regulatory submissions, and pharmacovigilance process improvements. This role is especially important for biosimilar products, where rigorous safety monitoring and regulatory compliance are essential to ensure patient safety and product reliability.For professionals with pharmacovigilance experience, this role offers exposure to global safety operations, regulatory frameworks, and advanced safety systems used in modern drug safety management.Job DescriptionAlvotech is seeking a Pharmacovigilance Specialist to support clinical safety and post-marketing pharmacovigilance activities within its Research and Development function. The selected candidate will join the Global Safety Data Management team and work closely with safety leaders to ensure accurate management of safety data for clinical trials and marketed products. The role includes monitoring adverse events, managing safety reports, ensuring regulatory compliance, and supporting pharmacovigilance system operations.This position also contributes to developing pharmacovigilance processes, supporting audits and inspections, and collaborating with internal and external stakeholders involved in drug safety and regulatory activities.Key Features of the Role• Work within global pharmacovigilance and safety data management• Exposure to clinical trial safety monitoring and post-marketing surveillance• Involvement in safety system configuration and lifecycle management• Opportunity to collaborate with global regulatory and clinical teams• Participate in pharmacovigilance process development and compliance initiatives• Contribute to safety monitoring for biosimilar pharmaceutical productsResponsibilitiesClinical Safety & Pharmacovigilance Activities• Manage assigned clinical safety and post-marketing pharmacovigilance activities• Handle Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) management• Support regulatory safety submissions and reporting requirements• Conduct literature monitoring and digital platform monitoring for safety signals• Perform pharmacovigilance reconciliations and safety data verification• Support activities related to EudraVigilance and XEVMPDSafety Systems & Data Management• Support configuration, validation, and lifecycle management of pharmacovigilance systems• Maintain safety databases and ensure accurate safety data management• Work with safety systems such as Oracle Argus Safety, ARISg Safety System, and Veeva Vault SafetyPharmacovigilance Process Management• Develop and maintain global pharmacovigilance procedures and workflows• Ensure compliance with international regulatory guidelines and internal SOPs• Monitor safety processes to maintain regulatory compliance across clinical programsCross-Functional Collaboration• Collaborate with pharmacovigilance teams involved in benefit-risk assessment and clinical safety• Work with internal departments such as Quality, Regulatory Affairs, IT, and Clinical Program Development• Coordinate with external pharmacovigilance service providers and business partnersTraining, Audits & Compliance• Deliver pharmacovigilance training to internal staff and external stakeholders• Support safety-related audits and regulatory inspections• Ensure documentation and processes meet global regulatory requirementsRequired QualificationsEducational Requirements• Master’s degree in Pharmaceutical Sciences, Pharmacy, Medicine, or Life SciencesExperience and Skills• Minimum 3 years of experience in Pharmacovigilance or Drug Safety• Experience working in safety data management functions• Hands-on experience in clinical trial safety and post-marketing pharmacovigilance• Knowledge of safety databases such as Argus, ARISg, or Veeva Vault Safety• Experience working with global pharmaceutical products and clinical trials• Familiarity with biologic or combination products is an advantageRegulatory Knowledge• Strong understanding of global pharmacovigilance regulations and guidelines including• ICH Guidelines• FDA Regulations• GVP Guidelines• GCP Guidelines• CIOMS GuidelinesProfessional Skills• Strong organizational and time-management skills• Excellent communication and interpersonal abilities• Ability to work independently and manage multiple safety activities• Capability to collaborate effectively in multicultural and global teamsSalary InsightsAlthough the exact salary has not been disclosed, Pharmacovigilance Specialist roles in the global biopharmaceutical industry typically offer competitive compensation based on experience, expertise, and geographic location. Additional benefits may include international exposure, professional development opportunities, and involvement in global clinical programs for biosimilar medicines.Company OverviewAlvotech is a fully integrated specialty biopharmaceutical company dedicated to the development and manufacturing of high-quality biosimilar medicines.The company focuses on improving patient access to biologic treatments by developing cost-effective biosimilars while maintaining strict regulatory and quality standards. Within its Research and Development division, the Integrated Clinical and Medical Research department develops strategies aligned with global biosimilar guidelines and regulatory authority requirements. Through innovative clinical programs and strong pharmacovigilance systems, Alvotech ensures the safety, effectiveness, and regulatory compliance of its products worldwide.FAQsWho can apply for this role?Candidates with a Master’s degree in Pharmacy, Life Sciences, or Medicine and at least 3 years of pharmacovigilance experience.What type of work will the PV Specialist perform?The role includes clinical safety monitoring, adverse event management, safety data analysis, regulatory submissions, and pharmacovigilance system management.Is experience with safety databases required?Yes. Experience with safety systems such as Argus, ARISg, or Veeva Vault Safety is highly preferred.Does the role involve working with clinical trials?Yes. The role involves safety monitoring for clinical trials and post-marketing programs.Application Tips• Highlight your pharmacovigilance experience and safety data management expertise• Mention experience working with safety databases such as Argus or Veeva Vault Safety• Include knowledge of global PV regulations such as ICH, GVP, and GCP guidelines• Demonstrate experience managing ICSRs, SAE reporting, and safety monitoring• Emphasize your ability to collaborate with global teams and maintain regulatory compliance

Why This Role MattersPharmacovigilance and post-market safety monitoring are essential for protecting consumers and ensuring that healthcare and wellness products remain safe after they reach the market. Safety professionals play a critical role in analyzing adverse event data, identifying potential risks, and ensuring compliance with global regulatory requirements.The Senior Associate – Global Market Vigilance (GMV) position at Unilever within Unilever R&D Bangalore offers an excellent opportunity for experienced pharmacovigilance professionals to contribute to consumer safety initiatives across global markets. Working under the Global Regulatory Affairs function of the Wellbeing Collective, the role focuses on safety data analytics, signal detection, adverse event monitoring, and compliance reporting. By transforming complex safety datasets into actionable insights, the Senior Associate supports proactive risk management and helps ensure that consumer products meet the highest safety standards. This role is particularly important because it supports end-to-end post-market surveillance activities, helping organizations identify emerging safety signals early and take appropriate action to protect consumers worldwide.Job DescriptionUnilever is seeking a Senior Associate – Global Market Vigilance to support pharmacovigilance and safety monitoring activities for products managed by the Wellbeing Collective. The selected candidate will analyze adverse event data, identify safety trends, build dashboards, and support regulatory reporting processes. The role requires strong analytical expertise and hands-on experience working with safety databases such as Veeva Vault Safety. The position also requires collaboration with cross-functional teams across regulatory affairs, R&D, quality assurance, and consumer care to maintain data integrity, regulatory compliance, and proactive safety monitoring.Key Features of the Role• Work within Global Regulatory Affairs and pharmacovigilance operations• Focus on safety data analytics, signal detection, and trend monitoring• Use advanced safety databases such as Veeva Vault Safety• Collaborate with cross-functional teams including R&D, Quality, and Regulatory Affairs• Contribute to global post-market surveillance and consumer safety programs• Opportunity to mentor junior team members and support analytics initiativesResponsibilitiesSafety Data Analytics, Trending & Signal Detection• Lead trending and signal detection activities across global adverse event datasets• Conduct quantitative and qualitative analysis of safety data to identify emerging risks• Develop dashboards, safety scorecards, and trend reports for stakeholders• Use statistical and analytical tools to generate predictive insights and early warning indicators• Support signal validation and risk assessment for potential safety concerns• Collaborate with analytics teams to improve data automation and visualizationCase Management & Compliance• Manage intake, triage, and documentation of adverse event complaints using Veeva Vault Safety• Perform causality and seriousness assessments for safety events• Ensure timely escalation of potential serious adverse events• Conduct duplicate checks and maintain data quality reviews• Maintain compliance with global adverse event reporting standards and internal SOPsSystem & Process Optimization• Support configuration and validation of safety database updates• Recommend improvements to enhance safety analytics readiness and data accuracy• Conduct audits and reconciliation of safety dataCross-functional Collaboration & Leadership• Act as a point of contact for Regulatory Affairs, R&D, Quality, and customer experience teams• Present safety insights and risk indicators in cross-functional meetings• Mentor junior team members on analytics methods and case processing• Support corrective and preventive actions related to safety operationsReporting & Insights• Generate and review safety reports, dashboards, and KPI summaries• Interpret safety data and develop analytical insights• Support regulatory submissions and product safety reviews• Provide recommendations based on safety trend analysisRequired QualificationsEducational Requirements• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related fieldExperience and Skills• 5–8 years of experience in pharmacovigilance or drug safety• Hands-on experience with safety databases such as Veeva Vault Safety• Strong knowledge of MedDRA coding standards• Experience with global adverse event reporting requirements• Demonstrated expertise in safety data analytics, signal detection, and dashboard development• Strong analytical and problem-solving abilities• Ability to communicate complex safety insights clearly to stakeholdersSalary InsightsWhile the exact salary package has not been disclosed, senior pharmacovigilance roles in Bangalore with 5–8 years of experience typically offer competitive compensation depending on expertise and company standards.Common benefits may include competitive pay, performance incentives, professional development opportunities, exposure to global safety operations, and career advancement within regulatory affairs and pharmacovigilance.Company OverviewUnilever is one of the world’s leading consumer goods companies, operating in more than 190 countries and serving billions of consumers every day. The organization develops products across categories such as nutrition, personal care, and wellbeing.Through Unilever R&D Bangalore, the company drives research, innovation, and regulatory excellence for global markets. The Global Regulatory Affairs team ensures that products meet strict safety standards while maintaining consumer trust and regulatory compliance. Unilever is also recognized for its commitment to sustainability, diversity, and inclusive workplace practices.FAQsWho can apply for this role?Professionals with 5–8 years of pharmacovigilance experience and a degree in Pharmacy or Life Sciences.Is experience with Veeva Vault Safety required?Yes. Hands-on experience with Veeva Vault Safety or similar pharmacovigilance databases is preferred.What type of work will this role involve?The role focuses on safety data analytics, signal detection, adverse event management, and regulatory reporting.Is this a leadership role?Although it is an individual contributor role, the position involves mentoring junior staff and collaborating with multiple cross-functional teams.Application Tips• Highlight your pharmacovigilance experience and safety analytics expertise• Mention your experience with Veeva Vault Safety or other safety databases• Include knowledge of MedDRA coding and global adverse event reporting standards• Showcase experience in safety dashboards, signal detection, or data analytics projects• Emphasize your ability to analyze complex datasets and communicate insights clearly to stakeholders.

Why This Role MattersThe General Dentist plays an important role in maintaining patients’ oral health by diagnosing dental conditions, performing routine dental procedures, and educating patients about proper oral hygiene. This role helps ensure accessible and quality dental care while building strong patient relationships within the community.Job DescriptionHealthy Dental Clinicv is seeking a General Dentist for a full-time or part-time on-site role in Bengaluru. The selected candidate will provide comprehensive dental care, perform common dental procedures, and communicate effectively with patients to ensure a positive clinical experience at the clinic located near Old Madras Road.Key Features of the Role• Position: General Dentist• Company: Healthy Dental Clinicv• Location: Bangalore City, Bengaluru, Karnataka, India• Employment Type: Full-Time or Part-Time• Workplace Type: On-site• Salary: ₹20,000 – ₹40,000 per month• Expected Work Hours: Approximately 48 hours per weekResponsibilities• Diagnose dental issues through patient examinations and assessments• Perform basic dental procedures such as root canal treatments (RCT), fillings, crown preparations, and simple extractions• Provide patient consultations and develop appropriate treatment plans• Educate patients on oral hygiene and preventive dental care• Maintain accurate patient records and treatment documentation• Ensure proper sterilization and compliance with dental safety protocols• Use basic computer systems for patient records and clinic management• Communicate effectively with patients to ensure a comfortable treatment experienceRequired Qualification• Bachelor of Dental Surgery (BDS) or equivalent dental qualification from a recognized institutionImportant Requirements• Strong knowledge of basic dental procedures including RCT, extractions, fillings, and crown preparation• Good patient communication and interpersonal skills• Basic computer skills for clinic documentation and workflow• Proficiency in English and Kannada or Telugu• Ability to work effectively in a clinical team environmentWhat We Offer• Opportunity to work in a reputed dental clinic environment• Flexible employment options (full-time or part-time)• Competitive salary based on experience and skills• Opportunity to build clinical experience in general dentistry• Supportive workplace environmentExperience and Skills• General dentistry procedures• Root canal treatments (RCT)• Crown preparation and restorative dentistry• Dental extractions and fillings• Patient consultation and treatment planning• Clinical documentation and computer-based record managementSalary Insights• Monthly Salary: ₹20,000 – ₹40,000• Salary may vary depending on experience, clinical skills, and working hoursCompany OverviewHealthy Dental Clinicv is a dental clinic located in Bengaluru that focuses on providing comprehensive and accessible dental care services. The clinic offers a range of routine and restorative dental treatments while prioritizing patient comfort, quality care, and professional clinical practices.FAQsWhat qualification is required for this role?Candidates must have a Bachelor of Dental Surgery (BDS) or an equivalent dental qualification.What procedures will the General Dentist perform?The dentist will perform procedures such as root canal treatments, simple extractions, fillings, and crown preparations.Is this a full-time or part-time job?The clinic offers both full-time and part-time employment options.What languages are preferred for this role?Candidates should be proficient in English and Kannada or Telugu.Application Tips• Highlight experience performing RCT, fillings, and crown preparations• Mention strong patient communication skills• Include any experience using digital systems or dental software• Emphasize proficiency in English and Kannada or Telugu• Showcase experience in general dentistry procedures

Why This Role MattersMedical Affairs professionals play a vital role in connecting scientific knowledge with clinical practice, regulatory compliance, and commercial strategy. They ensure that pharmaceutical products are supported by accurate scientific evidence, regulatory documentation, and meaningful engagement with healthcare professionals.Job DescriptionPharmed Limited is hiring an Assistant Manager – Medical Affairs in Bangalore, Karnataka. This role involves medical writing, regulatory support, clinical research coordination, and collaboration with healthcare professionals and key opinion leaders (KOLs). The position is suitable for professionals with experience in pharmaceutical medical affairs, regulatory submissions, and scientific communication.Key Features of the Role• Position: Assistant Manager – Medical Affairs• Company: Pharmed Limited• Location: Bangalore, Karnataka, India• Industry: Pharmaceutical / Medical Affairs• Employment Type: Full-Time• Experience Required: 6 Months – 3 YearsResponsibilities• Support preparation of regulatory dossiers for new product submissions and respond to regulatory authority queries such as CDSCO.• Prepare and present regulatory submissions to advisory or expert committees when required.• Develop and maintain FSSAI product dossiers for regulatory and customer inquiries.• Track regulatory developments and present updates to management.• Respond to product-related medical queries from healthcare professionals and the marketing team.• Review and approve medical content used in brand promotional materials and digital marketing.• Develop monographs, training manuals, and CME slide decks for product launches.• Review scientific literature and prepare study summaries for management and marketing teams.• Develop scientific presentations for medical education programs and CMEs.• Conduct surveys and market research on new product concepts with Key Opinion Leaders (KOLs).• Coordinate with KOLs and Contract Research Organizations (CROs) for clinical studies and manuscript writing.• Participate in planning and conducting clinical studies and trials.• Support pharmacovigilance activities including adverse event reporting, safety monitoring, and PSUR coordination.Required Qualification• Postgraduate degree in Pharmacy, Pharmacology, Pharmaceutics, Mac . Pharmacology, Pharm.D, or equivalent.Important Requirements• 6 months to 3 years of experience in Medical Affairs, Regulatory Affairs, or Medical Writing within the pharmaceutical industry.• Experience with CDSCO or FSSAI regulatory submissions is preferred.• GCP certification or pharmacovigilance training is an advantage.• Prior experience working with KOLs or CROs is beneficial.What We Offer• Opportunity to work in pharmaceutical medical affairs and regulatory functions.• Exposure to clinical research, regulatory submissions, and medical communication.• Collaboration with healthcare professionals, KOLs, and research organizations.Experience and Skills• Medical and scientific writing• Medico-marketing communication and content development• Regulatory dossier preparation (CDSCO, FSSAI)• Clinical research and trial coordination• Pharmacovigilance support and adverse event reporting• Proficiency in MS Office (Word, Excel, PowerPoint)• Strong analytical thinking and scientific literature interpretation• Excellent written and verbal communication skillsCompany OverviewPharmed Limited is a pharmaceutical organization involved in developing and supporting healthcare products through scientific research, regulatory compliance, and medical affairs initiatives. The company works closely with healthcare professionals and regulatory bodies to ensure product quality, safety, and effective communication of medical information.FAQsWhat qualification is required for this role?Candidates must have a postgraduate degree in Pharmacy, Pharmacology, Pharmaceutics, Pharm.D, or a related field.How much experience is required?The role requires 6 months to 3 years of experience in medical affairs, regulatory affairs, or medical writing.Where is the job located?The position is based in Bangalore, Karnataka, India.Does the role involve travel?Yes, occasional travel may be required for meetings with KOLs, CRO coordination, and scientific conferences.Application Tips• Highlight postgraduate qualifications in pharmacy or pharmacology.• Mention experience in regulatory submissions, medical writing, or clinical research.• Showcase knowledge of CDSCO and FSSAI regulations.• Emphasize skills in scientific communication and literature review.

Why This Role MattersAssociate Dentists play an important role in delivering quality dental care by assisting in diagnosis, performing basic dental procedures, and supporting patient treatment plans. In modern dental organizations, dentists also work with advanced technologies and collaborate with senior doctors to improve patient outcomes and clinical efficiency.Job DescriptionDezy is hiring an Associate Dentist to join its dental team in Bangalore, Karnataka. Dezy is a fast-growing dental health-tech company founded by IIT/IIM alumni and backed by leading investors. This role is suitable for freshers or dentists with up to 1 year of experience who are interested in working in a technology-driven dental care environment and gaining exposure to modern dental treatments.Key Features of the Role• Position: Associate Dentist• Company: Dezy• Location: Marathahalli, Vidyaranyapura, Jakkur – Bangalore City, Bengaluru, Karnataka, India• Industry: Health, Wellness & Fitness / Dental Care• Employment Type: Full-Time• Salary: ₹20,000 – ₹25,000 per month (with performance incentives)Responsibilities• Perform dental examinations and diagnose oral health conditions• Develop treatment plans in collaboration with senior dentists• Conduct basic dental procedures such as intraoral scans, cleanings, and fillings• Assist senior doctors during dental surgeries and complex procedures• Educate patients about oral hygiene, preventive care, and post-treatment care• Maintain accurate patient records, treatment plans, and medical histories• Coordinate with administrative teams to ensure smooth patient care• Call and coordinate with patients for home or partner clinic scan appointments• Upload scan files and intraoral/extraoral photos within the specified turnaround time• Participate in trade fairs and outreach activities to build relationships with dental clinics and professionals• Stay updated with advancements in dentistry including aligners and dental implantsRequired Qualification• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid dental license to practice in IndiaImportant Requirements• Freshers or candidates with up to 1 year of clinical experience• Strong communication and interpersonal skills• Patient-focused approach and empathy• Ability to work in a collaborative team environment• Interest in digital dentistry and modern dental technologiesWhat We Offer• Opportunity to work in a rapidly growing dental health-tech startup• Exposure to advanced dental technologies and digital consultations• Performance-based incentives in addition to base salary• Learning and development opportunities in aligners, implants, and modern dentistryExperience and Skills• 0–1 year of clinical experience• Skills in dental examination and treatment planning• Basic clinical procedures such as scanning, cleaning, and fillings• Patient consultation and communication skills• Ability to maintain accurate clinical recordsCompany OverviewDezy is a rapidly growing dental health-tech company founded in 2019 by IIT and IIM alumni. Backed by investors such as Falcon Edge (Alpha Wave Ventures), Sequoia Capital India, and Chiratae Ventures, the company aims to build one of India and GCC’s most trusted dental care brands. Dezy combines technology and dentistry to provide transparent diagnoses, digital consultations, and high-quality dental treatments.FAQsWhat qualification is required for this role?Candidates must have a BDS degree and a valid dental license to practice in India.Are freshers eligible to apply?Yes, freshers and candidates with up to 1 year of experience can apply.What is the salary offered?The salary ranges from ₹20,000 to ₹25,000 per month along with performance incentives.What dental services does the company specialize in?Dezy specializes in invisible smile aligners, dental implants, smile makeovers, root canal treatments, teeth whitening, dental veneers, and digital dental consultations.Application Tips• Highlight your BDS qualification and internship clinical experience• Mention any exposure to digital dentistry or dental scanning technologies• Emphasize patient communication and teamwork skills• Showcase interest in modern dental treatments like aligners and implants

Why This Role MattersTechnical documentation plays a critical role in ensuring that complex scientific products and solutions are clearly understood and effectively used by customers worldwide. The Technical Writer position at Thermo Fisher Scientific supports the development of accurate, high-quality documentation for advanced bioscience products. By translating technical and scientific concepts into clear instructions, this role helps researchers, laboratories, and organizations operate more efficiently and safely.Working in a globally recognized scientific organization also offers exposure to cutting-edge bioscience innovations and collaborative work with cross-functional teams. This role contributes to improving product usability, maintaining regulatory standards, and supporting scientific advancements that impact healthcare, research, and environmental safety worldwide.Job DescriptionThe Technical Writer I will be responsible for developing, editing, and maintaining comprehensive technical documentation for bioscience products and solutions. This includes creating user guides, manuals, and instructional content that clearly explain complex scientific procedures and technologies.The role requires close collaboration with teams such as research and development, product management, regulatory affairs, and quality assurance to ensure documentation accuracy and completeness. The Technical Writer will also be responsible for maintaining documentation standards, improving existing materials, and managing multiple documentation projects simultaneously.This position demands strong writing skills, attention to detail, and the ability to interpret technical scientific information and convert it into user-friendly content.Key Features of the Role:• Opportunity to work with a leading global life sciences organization• Exposure to cutting-edge bioscience products and technologies• Collaboration with cross-functional teams including R&D and regulatory departments• Opportunity to improve scientific communication and documentation skills• Work on global documentation projects supporting international customers• Career growth opportunities in scientific documentation and technical communicationResponsibilities• Develop, write, and edit technical documents including user manuals, product guides, and technical documentation for bioscience products• Collaborate with subject matter experts, scientists, and product teams to gather technical information• Translate complex scientific data and product details into clear, easy-to-understand documentation• Review and revise existing documentation to improve clarity, accuracy, and usability• Ensure all documents comply with company documentation standards and industry best practices• Manage multiple documentation projects simultaneously while meeting project deadlines• Maintain document repositories, templates, and version control systems• Support continuous improvement of documentation processes and standards• Ensure documentation supports product usability, safety, and regulatory complianceRequired QualificationsEducational Requirements:• Bachelor’s degree in Biosciences, Life Sciences, Biotechnology, Pharmacy, or a related scientific field• Advanced degree in biosciences or related discipline may be preferred• Certification in technical writing or scientific documentation can be an added advantageExperience and Skills:• Experience in technical writing, preferably within the bioscience or life sciences industry• Ability to translate complex scientific information into clear technical documentation• Strong written and verbal communication skills• Excellent attention to detail and documentation accuracy• Familiarity with XML or DITA-based authoring tools such as Oxygen XML Editor or similar platforms• Experience with component content management systems like RWS Tridion Docs or similar tools• Knowledge of Microsoft Office tools including Word, Excel, and PowerPoint• Familiarity with Adobe Creative Suite and other documentation tools• Ability to collaborate effectively with cross-functional teams and subject matter experts• Strong time-management skills and ability to manage multiple projects simultaneously• Willingness to continuously learn new tools, technologies, and documentation standardsSalary Insights:• Entry-level professionals may earn approximately ₹4 LPA – ₹7 LPA• Candidates with relevant experience may earn ₹7 LPA – ₹10 LPA or higher depending on expertise and location• Additional benefits may include health insurance, training programs, and performance incentivesCompany OverviewThermo Fisher Scientific is a global leader in scientific research solutions, laboratory technologies, analytical instruments, and life sciences services. The company supports scientists, researchers, healthcare organizations, and pharmaceutical companies worldwide with innovative products and solutions.With a mission to make the world healthier, cleaner, and safer, Thermo Fisher Scientific provides advanced technologies that accelerate scientific discovery, improve healthcare outcomes, and support environmental sustainability. The company operates globally and collaborates with research institutions and organizations to advance scientific innovation.FAQsWhat does a Technical Writer do in the bioscience industry?A Technical Writer prepares manuals, guides, and product documentation that explain complex scientific products and technologies to end users in a clear and understandable manner.Is prior technical writing experience required?Yes, most organizations prefer candidates with experience in technical writing, especially in life sciences, biotechnology, or bioscience fields.What skills are important for this position?Strong writing skills, scientific knowledge, attention to detail, and the ability to simplify complex technical information are essential for success in this role.What tools are commonly used in technical writing roles?Technical writers often use XML-based authoring tools, documentation management systems, Microsoft Office applications, and graphic editing software.Application Tips• Highlight your technical writing or scientific documentation experience in your resume• Emphasize your educational background in biosciences, biotechnology, or pharmacy• Include examples of documentation, manuals, or writing projects you have worked on• Demonstrate familiarity with documentation tools and content management systems• Showcase your ability to work with scientific teams and translate complex information into simple instructions.