Pune Healthcare Jobs

Why This Role MattersClinical trials require strict documentation practices to ensure transparency, regulatory compliance, and patient safety. The Clinical Document Specialist plays a crucial role in managing and maintaining the Trial Master File (TMF), which contains essential documents that demonstrate the proper conduct of clinical studies.This role ensures that clinical trial documents are accurately filed, reviewed, and maintained within electronic Trial Master File systems. Proper document management is essential because regulatory authorities rely on these records during inspections to confirm that studies comply with international guidelines.Professionals in this role support clinical research teams by organizing documentation, maintaining inspection readiness, and ensuring that trial records remain accurate and complete throughout the study lifecycle. For life sciences graduates, this position offers a strong entry point into the clinical research and regulatory documentation field.Job DescriptionThe Clinical Document Specialist I is responsible for managing clinical trial documentation and maintaining the electronic Trial Master File (eTMF). The role involves reviewing essential study documents, indexing files, and ensuring that documentation meets regulatory and organizational standards.Working closely with clinical project teams and documentation leads, the specialist ensures that all documents are filed correctly and accessible when needed. This position requires strong attention to detail, excellent organizational skills, and a clear understanding of clinical research documentation practices.The role also involves assisting with system testing, resolving documentation issues, and supporting continuous improvement in document management workflows. By ensuring accurate and compliant documentation, the Clinical Document Specialist contributes significantly to the overall quality and integrity of clinical trials.Key Features of the Role:• Entry-level opportunity in clinical research documentation and TMF management• Hands-on experience with electronic Trial Master File (eTMF) systems• Exposure to global clinical trial regulatory standards and documentation processes• Collaboration with clinical research teams, project managers, and documentation leads• Opportunity to support system improvements and process optimization• Career development opportunities in clinical research operations and documentation managementResponsibilities• Review essential and non-essential Trial Master File (TMF) documents within the eTMF workflow• Perform initial indexing and accurate filing of clinical documents in the eTMF system• Ensure documentation meets company quality thresholds and productivity targets• Verify that documents comply with regulatory standards and sponsor requirements• Maintain updated study trackers and document logs for project management teams• Communicate regularly with Clinical Document Team Leads regarding project queries and documentation updates• Support User Acceptance Testing (UAT) activities during system upgrades or product development• Identify documentation workflow challenges and suggest process improvements• Ensure that documents are correctly classified according to TMF structure and regulatory guidelines• Coordinate with internal teams and stakeholders to resolve documentation issues• Maintain accurate records to ensure inspection readiness for clinical trialsRequired QualificationsEducational Requirements:• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related biomedical field• Degrees such as BSc, MSc, B.Pharm, M.Pharm, or Pharm.D are commonly considered suitable for this roleExperience and Skills:• 0–1 year of experience in the life sciences, clinical research, or healthcare industry• Basic understanding of clinical trial phases and clinical development processes• Knowledge of clinical documentation practices and Trial Master File structure• Familiarity with ICH-GCP guidelines and regulatory compliance requirements• Proficiency in Microsoft Office tools such as Word, Excel, and Outlook• Knowledge of eClinical technologies or eTMF systems is considered an advantage• Strong written and verbal communication skills in English• High attention to detail and strong organizational abilities• Ability to manage documentation accurately and maintain quality standards• Good coordination skills for working with internal teams and project stakeholdersSalary Insights:• Professionals with relevant experience in TMF management or clinical documentation may earn higher compensation• Additional benefits may include training programs, performance bonuses, and career development opportunitiesCompany OverviewClinical Document Specialist roles are commonly available in global Contract Research Organizations (CROs), pharmaceutical companies, and clinical research service providers operating in India. These organizations support the development of new medicines by managing clinical trials, maintaining regulatory documentation, and ensuring compliance with international standards.The clinical documentation function plays a key role in ensuring that all study-related information is organized, traceable, and available for regulatory review. Professionals working in this field contribute directly to maintaining the integrity and transparency of clinical research operations.FAQsWhat does a Clinical Document Specialist do?A Clinical Document Specialist manages and reviews clinical trial documentation, ensuring that files are properly organized within the Trial Master File and comply with regulatory standards.What is a Trial Master File (TMF)?The Trial Master File is a collection of essential documents that demonstrate how a clinical trial was conducted and managed according to regulatory requirements.Is prior clinical research experience required for this role?Many entry-level roles accept candidates with little or no experience, provided they have relevant life sciences education and knowledge of clinical documentation processes.What career opportunities can follow this role?Professionals may progress into roles such as TMF Specialist, Clinical Trial Associate, Clinical Project Coordinator, Clinical Data Specialist, or Clinical Operations Associate.Application Tips• Highlight your knowledge of clinical research documentation and ICH-GCP guidelines• Include any training or coursework related to clinical research or regulatory affairs• Emphasize strong attention to detail and document management skills• Mention familiarity with eClinical systems or electronic document management platforms• Demonstrate good communication skills and ability to coordinate with cross-functional teams.

Why This Role MattersHealthcare organizations rely heavily on accurate data to deliver quality patient care, maintain regulatory compliance, and support efficient medical record management. In the healthcare revenue cycle and information management ecosystem, accurate data entry and validation processes play a crucial role in ensuring reliable healthcare documentation and operational efficiency.The Healthcare Data Analyst – ROI Operations role supports healthcare providers and organizations by ensuring that medical records and healthcare data are processed accurately, securely, and in compliance with regulatory requirements. This role contributes directly to maintaining data integrity, protecting patient information, and enabling healthcare organizations to access critical information efficiently.Working with healthcare data also requires strict adherence to privacy standards such as the Health Insurance Portability and Accountability Act (HIPAA). Professionals in this role help maintain confidentiality while ensuring that healthcare data is processed accurately for operational and compliance purposes. At MRO Corp, the Analyst – ROI Operations position supports healthcare information workflows, improves operational efficiency, and contributes to delivering high-quality services to healthcare clients.Job DescriptionThe Healthcare Data Analyst – ROI Operations is responsible for performing accurate healthcare data entry, validation, and analysis tasks while maintaining strict compliance with healthcare regulations and company standards. The role requires strong attention to detail, data processing accuracy, and the ability to work efficiently within target-driven operational environments.The selected candidate will manage healthcare data entry processes, ensure database accuracy, support operational reporting, and collaborate with internal teams to improve data workflows. The role also involves maintaining internal databases, monitoring key performance indicators (KPIs), and ensuring that data integrity standards are consistently met.Key Features of the Role• Job Title: Healthcare Data Analyst – ROI Operations / Healthcare Data Entry Analyst• Company: MRO Corp• Work Type: Full-Time, Office-Based• Work Schedule: 5 Days per Week• Experience Level: Entry-Level to Early Career• Industry: Healthcare Information Management / Revenue Cycle ManagementResponsibilities• Perform accurate healthcare data entry and validation processes according to healthcare regulations and internal standards.• Maintain data integrity by ensuring that healthcare information is accurate, complete, and consistent.• Update and maintain internal databases to ensure data quality and proper documentation.• Collaborate with team members to achieve operational targets and productivity goals.• Work efficiently in different shifts while managing workload in a fast-paced environment.• Assist in analyzing healthcare data and improving data entry processes to enhance operational efficiency.• Follow data entry best practices to reduce errors and maintain quality standards.• Maintain professionalism and attention to detail while handling healthcare information.• Support operational teams in refining data workflows and improving system performance.Key Performance Indicators (KPIs)• Data Accuracy: Maintain high standards of data entry accuracy and eliminate errors to ensure quality healthcare data management.• Productivity Improvement: Monitor individual productivity and continuously improve efficiency in data processing tasks.• Knowledge Application: Apply job knowledge effectively to meet project objectives and operational targets.• Compliance Adherence: Stay informed about regulatory updates, client expectations, and company policies.Required QualificationsEducational Requirements• B.Sc (Life Sciences or related fields)• B.Pharm (Bachelor of Pharmacy)• BA (Bachelor of Arts)• Nursing• Other Life Science or healthcare-related degreesExperience and Skills• 0–3 years of experience in US healthcare processes such as Release of Information (ROI), medical billing, or revenue cycle management.• Basic understanding of healthcare compliance regulations including the Health Insurance Portability and Accountability Act (HIPAA).• Strong attention to detail and data entry accuracy.• Experience working in fast-paced, target-driven environments.• Proficiency in Microsoft Office tools such as Word, Excel, and Outlook.• Knowledge of data entry best practices and healthcare documentation standards.• Familiarity with healthcare data processing platforms or software tools is an added advantage.Additional Preferred Experience• Experience in healthcare document retrieval processes.• Exposure to Release of Information (ROI) operations.• Understanding of healthcare revenue cycle processes such as claims adjudication, claims adjustment, or medical billing.Salary InsightsThe salary for Healthcare Data Analyst – ROI Operations roles typically depends on experience, organization policies, and location.Estimated Salary Range: • ₹2,50,000 – ₹4,00,000 per yearAdditional benefits may include: • Professional exposure to healthcare information management systems• Experience in US healthcare operations and compliance standards• Opportunities for career growth in healthcare analytics and revenue cycle management• Skill development in healthcare data processing and regulatory complianceCompany OverviewMRO Corp is a leading provider of healthcare information management services that help healthcare organizations securely exchange medical records and patient information. The company specializes in Release of Information (ROI) services, healthcare data management, and compliance-driven data processing solutions.By partnering with healthcare providers, hospitals, and medical institutions, MRO Corp ensures accurate medical record management while maintaining strict regulatory compliance and data security standards. The organization plays a key role in improving healthcare data accessibility, operational efficiency, and patient information management.FAQs1. What does a Healthcare Data Analyst – ROI Operations do?This role involves entering, validating, and managing healthcare data while ensuring compliance with healthcare regulations and maintaining database accuracy.2. Is prior healthcare experience required?Candidates with 0–3 years of experience in US healthcare processes such as ROI, medical billing, or RCM are preferred, but entry-level candidates may also apply.3. What skills are important for this role?Key skills include data entry accuracy, attention to detail, knowledge of healthcare compliance standards, analytical thinking, and proficiency in Microsoft Office tools.4. Is this a remote job?No. This is a full-time office-based role with a five-day work schedule.5. What career growth opportunities are available?Professionals can progress to roles such as Senior Healthcare Data Analyst, Healthcare Operations Specialist, or Revenue Cycle Analyst.Application Tips• Highlight experience in healthcare data entry, medical billing, or ROI processes if applicable.• Demonstrate familiarity with healthcare compliance regulations such as HIPAA.• Showcase proficiency in Microsoft Excel and data processing tools.• Emphasize attention to detail and accuracy in handling healthcare information.• Mention any experience working in target-driven operational environments.

Why This Role MattersIn modern healthcare systems, patients often require prior approval from insurance providers before certain medications or treatments can be dispensed. This process, known as prescription prior authorization, ensures that therapies are medically necessary, safe, and aligned with insurance coverage policies. Without proper authorization, patients may face delays in receiving essential medications or incur higher treatment costs.The role of a Prescription Prior Authorization Specialist is crucial in bridging the gap between healthcare providers, insurance companies, pharmacies, and patients. By coordinating authorization requests and verifying coverage requirements, professionals in this role help ensure that patients receive timely access to prescribed medications.Pharmacy professionals bring valuable knowledge to this position because they understand drug therapy, prescription processes, and healthcare documentation. Their expertise allows them to interpret prescription requirements, communicate effectively with healthcare teams, and navigate authorization systems efficiently. This role supports patient care while improving administrative efficiency within healthcare organizations.Job DescriptionThe Prescription Prior Authorization Specialist is responsible for managing medication authorization requests, verifying insurance requirements, and coordinating with healthcare providers and insurers to obtain approval for treatments. The position involves reviewing prescription information, preparing required documentation, and submitting authorization requests to insurance companies or pharmacy benefit managers.Professionals in this role track authorization statuses, resolve issues related to coverage approvals, and ensure that all documentation complies with healthcare regulations. The specialist also communicates regularly with physicians, clinical staff, and patients to provide updates on authorization progress and requirements.This position is well suited for pharmacy graduates who are interested in healthcare support services, medical billing, pharmacy benefit management, or healthcare administration. It offers a structured career path within healthcare operations and insurance coordination while maintaining a strong connection to pharmacy practice.Key Features of the RoleThe role offers pharmacy professionals an opportunity to work in healthcare support services where they can apply their knowledge of medications, prescriptions, and healthcare documentation. Professionals in this position collaborate with multiple stakeholders, including healthcare providers, insurance companies, and patient support teams, to facilitate medication approvals.The job also involves working with healthcare documentation systems and insurance authorization workflows, helping professionals develop strong administrative, analytical, and communication skills. It provides exposure to pharmacy benefit management and healthcare insurance processes, which are growing sectors within the healthcare industry.Responsibilities• Managing prior authorization requests for medications and treatments.• Coordinating with healthcare providers, insurance companies, and patients.• Verifying insurance coverage and authorization requirements.• Preparing and submitting prior authorization documentation.• Tracking authorization status and ensuring timely approvals.• Communicating updates and requirements with physicians and clinical teams.• Maintaining accurate documentation and compliance with healthcare regulations.• Resolving authorization issues and following up on pending approvals.• Handling multiple authorization cases simultaneously while ensuring accuracy.• Ensuring adherence to organizational procedures and healthcare compliance standards.Required QualificationsEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Diploma in Pharmacy (D.Pharm)Experience and Skills• Minimum 1 year of experience in prescription prior authorization or related healthcare support roles.• Knowledge of prior authorization workflows and insurance approval processes.• Strong written and verbal communication skills.• Ability to coordinate with insurers, physicians, and healthcare teams.• Excellent organizational and multitasking abilities.• Familiarity with healthcare documentation and regulatory compliance standards.• Attention to detail in reviewing prescription and authorization documentation.• Ability to track multiple cases and manage deadlines efficiently.• Strong problem-solving skills for resolving authorization issues.Salary InsightsThe salary offered for the Prescription Prior Authorization Specialist role typically depends on the candidate’s experience, skill level, and the hiring organization’s policies.Estimated salary range:• ₹2,80,000 – ₹4,50,000 per yearAdditional benefits may include:• Exposure to healthcare support and insurance coordination processes.• Professional development opportunities in medical billing and healthcare administration.• Stable career growth in pharmacy benefit management and healthcare operations.• Opportunities to work with healthcare providers, insurers, and clinical teams.Company OverviewHealthcare service organizations that hire Prescription Prior Authorization Specialists typically support hospitals, pharmacies, insurance companies, and healthcare providers in managing medication approval processes. These organizations help streamline administrative workflows and ensure patients receive medications without unnecessary delays. Such companies often specialize in medical billing, pharmacy benefit management, healthcare documentation, and insurance coordination services. By managing authorization processes efficiently, they play a critical role in improving healthcare delivery and ensuring regulatory compliance.FAQs1. What does a Prescription Prior Authorization Specialist do?They manage authorization requests for medications and treatments, coordinate with insurers and healthcare providers, and ensure approvals are processed efficiently.2. Who can apply for this role?Candidates with D.Pharm or B.Pharm qualifications and experience in prior authorization processes are eligible.3. Is prior authorization experience mandatory?Yes, most employers prefer candidates with at least one year of experience in prior authorization or related healthcare support roles.4. What career opportunities are available after this role?Professionals can advance to positions such as Senior Authorization Specialist, Healthcare Operations Analyst, Medical Billing Specialist, or Pharmacy Benefit Management Professional.Application Tips• Highlight your knowledge of prescription workflows and healthcare documentation.• Emphasize experience in prior authorization or insurance coordination.• Showcase strong communication skills for interacting with healthcare providers and insurers.• Demonstrate your ability to manage multiple cases while maintaining accuracy.• Mention any experience with healthcare management systems or insurance platforms.

Why This Role MattersThe Manager / Senior Executive – QA Validation plays a critical role in ensuring that biopharmaceutical manufacturing systems, utilities, and aseptic processes operate in full compliance with global regulatory standards. In highly regulated environments such as biologics and aseptic manufacturing, validation is fundamental to product quality, sterility assurance, and patient safety.This role ensures that equipment, instruments, HVAC systems, and critical utilities are properly qualified and maintained throughout their lifecycle. By aligning validation practices with cGMP, regulatory guidelines, and internal Quality Management Systems (QMS), the position strengthens audit readiness and inspection confidence.Through collaboration with Production, Engineering, Quality Control, and Regulatory teams, this role supports seamless technology transfer, process optimisation, and operational excellence. Ultimately, it safeguards compliance while enabling innovation within a biopharmaceutical manufacturing environment.Job DescriptionThe Manager / Senior Executive – QA Validation is responsible for planning, executing, reviewing, and approving validation and qualification activities across biopharmaceutical manufacturing operations. The role ensures that all validation activities follow regulatory expectations and internal quality standards.The candidate will provide QA validation oversight for equipment, instruments, AHUs, HVAC systems, aseptic filling operations, and other critical utilities. The role includes active participation in audits, regulatory inspections, deviation management, CAPA implementation, and continuous improvement initiatives.This position is suited for experienced QA Validation professionals with 6–9 years of experience in the biopharmaceutical industry and strong exposure to global regulatory inspections.Key Features of the Role:• Position: Manager / Senior Executive – QA Validation• Department: Quality Assurance• Industry: Biopharmaceutical Manufacturing• Qualification: M.Sc / M.Pharm• Experience Required: 6–9 years in QA Validation• Strong exposure to aseptic filling and HVAC validation• Hands-on regulatory audit experience (USFDA, EU, TGA, WHO)• Focus on lifecycle validation and compliance excellenceResponsibilitiesValidation & Qualification• Plan, execute, review, and approve equipment and instrument qualification activities (DQ, IQ, OQ, PQ)• Ensure effective execution of AHU qualification and HVAC validation• Prepare, review, and maintain validation documents as per the approved Validation Master Plan (VMP)• Support validation of critical utilities, systems, and manufacturing processes• Maintain validation lifecycle management in line with regulatory expectationsQuality Systems & Compliance• Ensure validation activities align with QMS and regulatory guidelines• Participate in deviation investigations, CAPA management, change controls, and risk assessments• Maintain data integrity and compliance across validation documentation• Ensure ongoing cGMP compliance in all validation processesAudit & Regulatory Support• Support and face regulatory inspections and customer audits (USFDA, EU, TGA, WHO, and other agencies)• Prepare responses to audit observations related to validation and qualification• Maintain audit readiness at all timesManufacturing & Operations Support• Provide QA validation oversight for aseptic filling operations and associated equipment• Collaborate with Production, Engineering, QC, and Regulatory teams• Support technology transfer and process improvement initiativesDocumentation & Continuous Improvement• Review SOPs, validation protocols, and reports• Drive continuous improvement initiatives to enhance validation efficiency• Strengthen compliance systems and process robustnessRequired QualificationsThe ideal candidate is a detail-oriented validation expert with deep technical knowledge of biopharmaceutical manufacturing processes and regulatory compliance frameworks.Educational Requirements:• M.Sc in Life Sciences / Biotechnology / Microbiology or related discipline OR• M.Pharm• Strong academic foundation in pharmaceutical validation and quality systemsExperience and Skills:• 6–9 years of experience in QA Validation within biopharmaceutical manufacturing• Strong experience in equipment qualification (DQ, IQ, OQ, PQ)• Hands-on experience in AHU and HVAC validation• Expertise in aseptic filling validation oversight• In-depth knowledge of cGMP and global regulatory requirements• Experience handling regulatory inspections (USFDA, EU, TGA, WHO)• Strong documentation and validation protocol review skills• Experience managing deviations, CAPA, and change control processes• Strong analytical and problem-solving abilities• Excellent cross-functional collaboration skills• High attention to detail and compliance-focused mindsetSalary InsightsCompensation will be competitive and aligned with industry standards based on experience and expertise in QA Validation within the biopharmaceutical sector. Candidates with regulatory inspection handling experience and aseptic validation exposure typically command strong market packages and growth opportunities within global pharmaceutical organisations.Company OverviewEnzene is an innovation-driven biopharmaceutical organisation committed to advancing healthcare through cutting-edge science and robust quality systems. The company emphasises regulatory excellence, advanced manufacturing technologies, and a culture of continuous improvement.At Enzene, employees are recognised as the organisation’s greatest asset. The company fosters a forward-looking culture powered by pioneers who are dedicated to transforming the pharmaceutical industry through innovation, operational excellence, and uncompromising quality standards.FAQsQ1. Is aseptic filling validation experience mandatory?Yes, hands-on experience in aseptic filling operations validation is strongly preferred.Q2. What regulatory exposure is required?Experience handling inspections from USFDA, EU, TGA, WHO, or other global agencies is expected.Q3. Is this role focused only on documentation?No. The role includes active shop floor validation oversight along with documentation review.Q4. What level of experience is suitable?Candidates with 6–9 years of relevant QA Validation experience in biopharmaceutical manufacturing are ideal.Q5. Does the role involve cross-functional coordination?Yes, close collaboration with Production, Engineering, QC, and Regulatory teams is required.Application Tips• Highlight experience in DQ, IQ, OQ, and PQ qualification activities• Mention AHU, HVAC, and aseptic validation exposure• Provide examples of regulatory inspection handling• Showcase deviation management and CAPA experience• Demonstrate knowledge of lifecycle validation principles• Emphasise cross-functional project coordination skills

Why This Role MattersThe Assistant Manager – Global QMS plays a strategic role in ensuring consistent quality standards across multiple sites within a regulated pharmaceutical or biotechnology organisation. A robust Global Quality Management System (QMS) is the backbone of regulatory compliance, operational excellence, and product reliability. This role ensures that quality frameworks are not only implemented but continuously improved to meet evolving global regulatory expectations.By overseeing document review, regulatory compliance monitoring, audit participation, and quality trend analysis, this position safeguards product integrity and patient safety on a global scale. The role bridges site-level operations with corporate quality objectives, ensuring alignment with GMP, ISO, ICH, FDA, WHO, and other applicable regulatory frameworks.Through strong governance, oversight, and collaboration with cross-functional teams, the Assistant Manager – Global QMS strengthens organisational readiness for inspections and drives a culture of quality excellence across the enterprise.Job DescriptionThe Assistant Manager – Global QMS is responsible for supporting the implementation, maintenance, and continuous improvement of the Global Quality Management System across all company sites. The role ensures alignment with internal standards and international regulatory requirements.The position requires active involvement in reviewing and approving quality documents, tracking regulatory commitments, supporting audits and inspections, and monitoring key quality metrics. The individual will collaborate with site Quality Assurance teams to ensure consistent interpretation and application of global quality standards.This role is ideal for experienced Quality Assurance professionals with strong exposure to global QMS frameworks within pharmaceutical, biotechnology, or other highly regulated industries.Key Features of the Role:• Position: Assistant Manager – Global QMS• Department: Quality Assurance• Qualification: M.Sc or M.Pharm• Experience Required: 9–12 years in QA / Global QMS• Industry: Pharmaceutical / Biotech / Regulated Industry• Exposure to global regulatory authorities (FDA, WHO, ICH, ISO, GMP)• Enterprise-wide quality system oversight• Opportunity to contribute to global compliance strategyResponsibilities• Ensure effective implementation and compliance of the Global Quality Management System across all sites• Review and approve quality documents including SOPs, policies, deviations, CAPAs, change controls, and risk assessments• Monitor adherence to global regulatory guidelines such as GMP, ISO, ICH, FDA, WHO, and local regulations• Track regulatory commitments and ensure timely closure of action items• Support and participate in internal audits, external audits, and regulatory inspections• Perform trend analysis of deviations, complaints, OOS/OOT events, and assess CAPA effectiveness• Coordinate with site QA teams to standardise interpretation and implementation of QMS procedures• Prepare quality metrics, dashboards, and reports for management review meetings• Drive continuous improvement initiatives within the Global QMS framework• Identify gaps in quality systems and recommend corrective and preventive actions• Maintain inspection readiness across all operational sites• Support enterprise-level quality governance and compliance initiativesRequired QualificationsThe ideal candidate is a seasoned Quality Assurance professional with strong exposure to global quality systems and regulatory compliance frameworks.Educational Requirements:• M.Sc in a relevant Life Sciences discipline OR• M.Pharm• Strong foundation in pharmaceutical quality systems and regulatory scienceExperience and Skills:• 9–12 years of relevant experience in Quality Assurance or Global QMS• Strong knowledge of global QMS frameworks and regulatory expectations• In-depth understanding of GMP and pharmaceutical quality systems• Experience handling audits and regulatory inspections• Strong analytical and problem-solving capabilities• Experience in deviation management, CAPA evaluation, and risk assessment• Proficiency in documentation control and quality metrics reporting• Ability to collaborate with cross-functional and multi-site teams• Strong written and verbal communication skills• Capability to drive quality improvements at an organisational levelSalary InsightsCompensation will be aligned with industry benchmarks and commensurate with experience and expertise in Global QMS and regulatory compliance. Senior-level exposure to enterprise-wide quality systems typically commands competitive remuneration packages, along with performance-based growth opportunities.Company OverviewEnzene is an innovation-driven pharmaceutical organisation committed to redefining healthcare solutions through advanced science and technology. The company focuses on regulatory excellence, operational efficiency, and a strong culture of quality.At Enzene, employees are regarded as the organisation’s most valuable asset. The company fosters a forward-thinking environment driven by pioneers who are dedicated to disrupting the pharmaceutical industry through innovation while maintaining stringent global quality and compliance standards.FAQsQ1. Is prior Global QMS experience mandatory?Yes, candidates should have substantial exposure to Global QMS or enterprise-level quality systems.Q2. What regulatory knowledge is expected?Strong understanding of GMP, ISO, ICH, FDA, WHO, and other applicable regulatory guidelines is required.Q3. Does the role involve audit participation?Yes, the role includes participation in internal audits, external audits, and regulatory inspections.Q4. Is this a site-level or global role?This is a global-level role supporting quality system implementation across all sites.Q5. What type of industry experience is preferred?Experience in pharmaceutical, biotechnology, or other regulated industries is preferred.Application Tips• Highlight enterprise-level QMS implementation experience• Mention audit and regulatory inspection exposure• Provide examples of managing deviations, CAPA, and risk assessments• Showcase experience preparing quality dashboards and management reports• Demonstrate cross-functional and multi-site coordination skills• Emphasise continuous improvement initiatives you have led

Why This Role MattersThe Executive / Senior Executive – Drug Substance Quality Assurance (DSQA) plays a critical role in ensuring that drug substance manufacturing operations consistently meet current Good Manufacturing Practice (cGMP) standards and global regulatory expectations. In a highly regulated pharmaceutical environment, maintaining quality at the shop floor level is essential to safeguarding product integrity, patient safety, and regulatory compliance.This role directly impacts the reliability of manufacturing processes by overseeing line clearance, reviewing batch documentation, monitoring in-process activities, and ensuring adherence to validated procedures. By actively participating in Quality Management System (QMS) processes such as deviations, change controls, and CAPA, the position supports continuous improvement and strengthens compliance culture.Working within a fast-evolving pharmaceutical organisation focused on innovation, this role contributes to building robust quality systems that support regulatory inspections, international market approvals, and sustainable growth in drug substance manufacturing.Job DescriptionThe Executive / Senior Executive – DSQA will be responsible for ensuring cGMP compliance at the shop floor for Drug Substance (DS) manufacturing operations. The position involves active oversight of manufacturing activities, review of documentation, validation support, and participation in quality systems processes.The candidate will work closely with production, quality control, engineering, and regulatory teams to ensure seamless compliance with established procedures and regulatory guidelines. The role requires strong technical knowledge of DS manufacturing processes, validation activities, and quality documentation systems.This position is based in Pune and is open to candidates with 2–9 years of relevant experience in pharmaceutical Quality Assurance, particularly in Drug Substance or Active Pharmaceutical Ingredient (API) environments.Key Features of the Role:• Position: Executive / Senior Executive – DSQA• Department: Quality Assurance• Location: Pune• Experience Required: 2–9 Years• Qualification: M.Sc / M.Pharm• Exposure to global regulatory standards (USFDA, EMA, WHO preferred)• Direct involvement in shop floor QA and QMS activities• Opportunity to work in an innovation-driven pharmaceutical organisationResponsibilities• Perform manufacturing line clearance activities for Drug Substance operations• Ensure proper execution and compliance of in-process checks during manufacturing• Conduct routine GMP rounds at the DS facility and document observations• Review online Batch Manufacturing Records (BMR) for accuracy, completeness, and compliance• Review and approve process validation and cleaning validation protocols and reports• Review and manage Standard Operating Procedures (SOPs) and related documentation• Coordinate sample collection and submission as per BMR, specifications, and validation protocols• Perform shop floor compliance rounds and track corrective actions• Prepare and support Annual Product Quality Review (APQR/PQR) documentation• Initiate and manage Change Controls, Deviations, Incidents, and CAPA• Participate in investigations, root cause analysis, and QMS improvement initiatives• Ensure regulatory readiness for audits and inspections• Conduct risk assessments for critical manufacturing and quality processes• Maintain continuous oversight to ensure adherence to cGMP standardsRequired QualificationsThe ideal candidate will be a detail-oriented and proactive Quality Assurance professional with strong exposure to Drug Substance manufacturing environments.Educational Requirements:• M.Sc in relevant Life Sciences discipline OR• M.Pharm• Strong academic foundation in pharmaceutical sciences and quality systemsExperience and Skills:• 2–9 years of experience in pharmaceutical Quality Assurance• Hands-on experience in DS or API shop floor QA activities• Strong understanding of cGMP and regulatory compliance requirements• Experience in BMR review and documentation control• Knowledge of process validation and cleaning validation• Familiarity with in-process control systems• Experience handling deviations, change controls, and CAPA• Strong analytical, investigation, and problem-solving abilities• Effective communication and cross-functional coordination skills• Ability to work in a dynamic, fast-paced manufacturing environmentSalary InsightsCompensation will be competitive and aligned with industry standards based on experience and qualifications. The organisation offers growth-oriented career opportunities, exposure to global regulatory environments, and a performance-driven work culture.Company OverviewEnzene is an innovation-driven pharmaceutical organisation committed to disrupting the pharmaceutical industry through cutting-edge solutions and advanced manufacturing capabilities. The company emphasises quality excellence, scientific innovation, and regulatory compliance while fostering a culture powered by pioneers and forward-thinking professionals.At Enzene, employees are regarded as the organisation’s greatest asset. The company promotes collaboration, accountability, and continuous improvement to support global regulatory standards and deliver high-quality pharmaceutical products to international markets.FAQsQ1. Is Drug Substance experience mandatory?Yes, hands-on exposure to DS or API shop floor QA activities is highly preferred.Q2. What regulatory exposure is expected?Experience with USFDA, EMA, WHO, or other global regulatory guidelines is preferred.Q3. Is this role focused on documentation only?No. The role includes active shop floor oversight along with documentation review and QMS activities.Q4. What level of experience is suitable?Candidates with 2 to 9 years of relevant QA experience are eligible.Q5. Is validation experience required?Yes, understanding and review of process validation and cleaning validation documentation is expected.Application Tips• Highlight direct experience in DS/API shop floor QA activities• Mention regulatory audit exposure (USFDA, EMA, WHO)• Provide examples of handling deviations, CAPA, and change control• Showcase validation documentation review experience• Emphasise involvement in risk assessment and QMS investigations• Demonstrate cross-functional collaboration with production and QC teams

Why This Role MattersThe Clinical Physiotherapist at Walnut Child Development Clinic plays a crucial role in improving the lives of children with developmental delays and behavioral disorders. This position contributes to early intervention, rehabilitation, and enhancing children’s overall quality of life through specialized pediatric physiotherapy within a multidisciplinary team.Job DescriptionWalnut Child Development Clinic, a leading pediatric rehabilitation chain in Pune, is hiring a full-time, permanent Clinical Physiotherapist for its Lohegaon center. The role involves working closely with a multidisciplinary team to deliver pediatric physiotherapy services for children with developmental and behavioral challenges. Immediate joiners willing to commit for a minimum of one year are preferred.Key Features of the Role• Position: Clinical Physiotherapist (Pediatric)• Organization: Walnut Child Development Clinic• Location: Lohegaon, Pune, Maharashtra (Tingre Nagar)• Employment Type: Full-Time, Permanent• Salary Range: ₹25,000 – ₹35,000 per month• Benefits: Paid leaves, Paid sick time, Annual bonus & incentives, Continuing education programsResponsibilities• Assess children with developmental delays and behavioral disorders• Develop individualized pediatric physiotherapy treatment plans• Deliver evidence-based physiotherapy interventions• Collaborate with multidisciplinary team members• Monitor progress and modify therapy plans accordingly• Educate parents and caregivers regarding home programs• Maintain clinical documentation and records• Participate in professional development and training programsRequired Qualification• Master’s Degree in Physiotherapy (MPT) – MandatoryEducational Requirement• MPT compulsoryImportant Requirements• Special interest in pediatric physiotherapy• Willingness to learn and grow professionally• Immediate joining preferred• Minimum one-year commitment required• Candidates preferably from Pune and nearby areas (NIBM, Fatima Nagar, Wanowrie, Undri, Pisoli, Mohammedwadi, Kondhwa, Katraj, Bibwewadi)Employment Options• Career growth in pediatric rehabilitation• Continuing education supportWhat We Offer• Competitive salary package• Paid time off and paid sick leave• Annual bonus and performance-based incentives• Continuing education programs• Opportunity to work in a reputed pediatric rehab chainExperience and Skills• Pediatric physiotherapy expertise• Strong assessment and treatment planning skills• Knowledge of developmental delay and behavioral disorders• Communication and caregiver counseling skills• Documentation and teamwork abilitiesSalary Insights• ₹25,000 – ₹35,000 per month• Additional annual bonus and incentives based on performanceCompany OverviewWalnut Child Development Clinic is a leading pediatric rehabilitation clinic chain in Pune specializing in developmental delay and behavioral disorder management. The clinic focuses on early intervention, multidisciplinary collaboration, and professional growth of therapists.FAQsWho can apply for this position?Candidates with a Master’s Degree in Physiotherapy (MPT) are eligible to apply.Is pediatric experience mandatory?While prior pediatric experience is preferred, candidates with strong clinical knowledge and willingness to learn may also apply.Is this a full-time role?Yes, this is a full-time permanent position.Is there any minimum commitment period?Yes, candidates are expected to commit for at least one year.What kind of patients will I be working with?Children with developmental delays and behavioral disorders.Are there any additional benefits?Yes, paid time off, paid sick leave, annual bonuses, incentives, and continuing education programs are provided.Is immediate joining required?Immediate joiners are preferred.Is location preference important?Yes, candidates from Pune and nearby areas are preferred.Application Tips• Highlight your MPT qualification clearly at the top of your resume.• Mention any pediatric internship or clinical exposure specifically.• Showcase experience in handling developmental delay or neuro cases.• Emphasize your communication skills with children and parents.• Include details about multidisciplinary teamwork experience.• Mention your willingness for a minimum one-year commitment.• Clearly state “Available for Immediate Joining” in your resume if applicable.

Why This Role MattersThe Clinical Safety Associate plays a crucial role in protecting patient health by ensuring the accurate collection, processing, and reporting of adverse event data from clinical trials and post-marketing sources. This position directly supports pharmacovigilance and Patient Safety Services (PSS) operations by managing expedited safety reports and maintaining regulatory compliance. Timely and accurate safety reporting is essential to meet global regulatory standards and to ensure that medicinal products remain safe for public use. By contributing to the end-to-end adverse event lifecycle, this role supports quality clinical research and strengthens trust between sponsors, regulatory authorities, and patients.Job DescriptionThe Clinical Safety Associate assists with overall Clinical Safety and PSS operations associated with pharmaceutical products. The role involves managing the entire adverse event process, including safety data collected from clinical trials and unsolicited post-marketing reports. The associate is responsible for processing expedited adverse events according to regulatory standards and submitting them to clients and regulatory authorities within agreed timelines. This position may function as part of a client project support team or operate as a standalone safety service provider. The role requires adherence to health, safety, and quality regulations as outlined in company policies and applicable legal frameworks.Key Features of the Role:• Involvement in clinical trial and post-marketing safety reporting• Hands-on exposure to adverse event lifecycle management• Opportunity to work with global regulatory authorities and ethics committees• Experience in MedDRA coding and narrative writing• Participation in Quality Management System (QMS) processes• Collaborative cross-functional working environment• Compliance-driven and timeline-sensitive operationsResponsibilities• Assist in processing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)• Maintain adverse event tracking systems and ensure accurate documentation• Set up and maintain project files and central documentation records• Report ESRs and PSRs to clients, regulatory authorities, ethics committees, and investigators within study timelines• Log all incoming Adverse Event (AE) and Serious Adverse Event (SAE) reports into departmental tracking systems• Perform accurate data entry of safety information into safety databases• Write detailed and medically accurate patient narratives• Code adverse events using MedDRA terminology where applicable• Assist in listedness assessment against approved product labeling• Generate follow-up queries for missing or inconsistent safety data in consultation with medical teams• Submit expedited SAE reports to clients, regulatory authorities, ethics committees, vendors, and partners within agreed timelines• Support peer and quality review of processed safety reports• Assist in reconciliation of safety databases• Maintain files related to country-specific adverse event reporting requirements• Work in compliance with Standard Operating Procedures (SOPs) and departmental Work Instructions (WIs)• Prepare safety study documentation for archiving at project completion• Coordinate internal and external meetings or teleconferences• Train and mentor PSS assistants or peers as required• Build and maintain strong professional relationships across functional units• Ensure compliance with regulatory requirements and project-specific safety plans• Take responsibility for data accuracy and quality• Provide administrative and operational support to PSS personnel• Perform additional duties as assignedRequired QualificationsCandidates should have an educational background in Life Sciences, Pharmacy, Nursing, Medical Sciences, or related disciplines. Equivalent industry experience may be considered in lieu of formal qualifications. Strong English communication skills (spoken and written) are mandatory, along with proficiency in the local language where applicable.Educational Requirements:• Non-degree qualification with 1–2 years of Safety or relevant industry experience, OR• Associate Degree with 6 months to 1 year of Safety or relevant experience, OR• Bachelor’s Degree (BS/BA) with 0–1 year of Safety or relevant experience, OR• Master’s Degree (MS/MA) with 0–6 months of Safety or relevant experience, OR• PharmD with 0–6 months of Safety experience• A one-year PharmD residency or fellowship may be considered as relevant experiencePreferred disciplines include Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related areas.Experience and Skills:• Experience in processing AE/SAE reports and working with safety databases is preferred• Familiarity with regulatory submissions and reporting timelines• Background in pharmaceutical, biotechnology, or CRO environments is advantageous• Strong attention to detail and commitment to data accuracy• Ability to prioritize tasks and manage multiple responsibilities simultaneously• Good logical reasoning and proofreading skills, especially for numerical data• Proficiency in MS Office and general computer applications• Strong written and verbal communication skills• Ability to work effectively in a team-oriented environment• Good keyboard and documentation management skills• Capability to operate standard office equipmentSalary InsightsThe compensation package is competitive and aligned with industry standards for entry-level to junior pharmacovigilance professionals. Salary may vary depending on qualifications, prior safety experience, technical expertise, and location. Additional benefits may include health coverage, performance incentives, and professional development opportunities.Company OverviewThe organization is a leading Contract Research Organization (CRO) specializing in clinical development and patient safety services. It provides comprehensive pharmacovigilance solutions, regulatory support, and clinical trial management to global pharmaceutical and biotechnology companies. With a strong commitment to regulatory compliance and quality standards, the company supports safe and efficient drug development across therapeutic areas.FAQsQ1. Is prior pharmacovigilance experience mandatory?Prior safety experience is preferred but not mandatory for candidates with relevant educational qualifications.Q2. What is Safety experience?Safety experience includes processing AE/SAE reports, narrative writing, database handling, and regulatory submission exposure.Q3. Is MedDRA knowledge required?Basic understanding of MedDRA coding is beneficial but may be developed during training.Q4. Is this role suitable for fresh graduates?Yes, candidates with 0–1 year of relevant experience may apply based on qualification criteria.Q5. What are the growth opportunities?Employees may progress to Senior Safety Associate, Drug Safety Officer, or Pharmacovigilance Specialist roles.Application Tips• Highlight experience in AE/SAE processing or clinical data management• Mention familiarity with safety databases and MedDRA terminology• Emphasize attention to detail and compliance awareness• Demonstrate understanding of regulatory timelines during interviews• Keep your resume structured, concise, and focused on relevant safety skills• Prepare examples showcasing teamwork and problem-solving abilities

Why This Role MattersThe Prosthodontist plays a critical role in restoring patients’ oral function, aesthetics, and confidence. At Clove Dental, this position ensures delivery of advanced prosthodontic care while maintaining global standards of hygiene, transparency, and clinical excellence.Job DescriptionClove Dental is hiring a Full-Time Prosthodontist for its clinics in Pune, Maharashtra (Aundh, Hinjewadi, Vishal Nagar zone). The role requires a skilled specialist with strong clinical expertise in prosthodontics and the ability to manage patients independently.Key Features of the Role• Position: Prosthodontist• Company: Clove Dental• Location: Aundh, Hinjewadi, Vishal Nagar – Pune, Maharashtra• Employment Type: Full-Time, Permanent• Salary: ₹40,000 – ₹55,000 per month• Work Setting: In-Clinic (On-site)• Experience: 2–3+ Years (Post-MDS)• Start: ImmediateResponsibilities• Diagnose and treat patients with missing or damaged teeth• Create comprehensive prosthodontic treatment plans• Design and fit crowns, bridges, dentures, and other dental prosthetics• Collaborate with dental technicians for functional and aesthetic outcomes• Educate patients on oral hygiene and maintenance• Maintain detailed patient records and clinical documentation• Stay updated with latest prosthodontic technologies and techniquesRequired Qualification• MDS – Prosthodontics• Valid State Dental LicenseEducational Requirement• Recognised MDS degree in ProsthodonticsImportant Requirements• Minimum 2–3+ years of clinical experience• Strong written and verbal communication skills• Comprehensive knowledge of dental procedures, tools, and diagnostics• Good management and patient-handling skills• Ability to maintain detailed clinical recordsEmployment Options• Full-Time• Permanent Role• In-person clinic-based positionWhat We Offer• Opportunity to work with India’s largest dental network• Structured clinical protocols and advanced equipment• Health insurance benefits• Professional growth and exposure to high patient volumeExperience and Skills• Practical experience in prosthetic restorations• Expertise in crowns, bridges, and dentures• Strong diagnostic capability• Effective communication skills• Clinic and patient management abilitySalary Insights• ₹40,000 – ₹55,000 per month• Salary may vary based on experience and expertiseCompany OverviewClove Dental is India’s largest dental clinic network, established in 2011, with 650+ clinics nationwide. The organization manages over 1 million patients per month and has conducted approximately 15 lakh treatments in the past decade. Equipped with state-of-the-art technology and strict hygiene protocols such as the Four-Step Sterilization Protocol, Clove Dental emphasizes trust, respect, integrity, and global standards of dental care.FAQsWho can apply?MDS Prosthodontics candidates with valid state license and 2–3+ years of experience.Is prior experience mandatory?Yes, a minimum of 2–3+ years post-MDS experience is required.What locations are available?Aundh, Hinjewadi, and Vishal Nagar in Pune, Maharashtra.Is this a full-time role?Yes, it is a full-time permanent in-clinic position.What benefits are provided?Health insurance is included.Application Tips• Highlight your MDS specialization clearly in your CV.• Mention the number and type of prosthetic cases handled.• Include details of advanced technologies or techniques used.• Emphasize patient communication and case documentation skills.• Keep your resume focused on prosthodontic expertise.

Why This Role MattersThe Senior Dentist plays a critical role in overseeing clinic operations while delivering high-quality dental care. This position ensures effective patient management, clinical excellence, and coordination among staff to maintain superior treatment standards.Job DescriptionClove Dental is hiring a Full-Time Senior Dentist for its clinics located in Tingre Bagar and Dhankawadi, Pune, Maharashtra. The role requires an experienced dental professional capable of managing daily operations, performing advanced dental procedures, and leading the clinical team.Key Features of the Role• Position: Senior Dentist• Company: Clove Dental• Location: Tingre Bagar & Dhankawadi, Pune, Maharashtra• Employment Type: Full-Time• Salary Range: ₹30,000 – ₹50,000 per month• Work Setting: Dental ClinicResponsibilities• Oversee daily clinic operations• Consult with patients to diagnose and treat dental concerns• Perform regular cleaning and preventive dental procedures• Develop treatment plans to improve oral hygiene• Order and interpret diagnostic measures such as X-rays and models• Use dental tools including drills, probes, brushes, and mirrors• Maintain detailed patient records and treatment documentation• Manage and coordinate with clinic staff for effective patient careRequired Qualification• BDS with minimum 3–4 years of experience OR• MDS with 1–2 years of experience• Valid State Dental LicenseExperience and Skills• Strong computer skills and experience with healthcare databases• Excellent written and verbal communication skills• Ability to maintain detailed clinical records• Comprehensive knowledge of dental procedures and diagnostics• Good management and leadership skillsImportant Remarks• Full-time position• Experience mandatory as per qualification criteria• Posting locations: Tingre Bagar & Dhankawadi – PuneSalary Insights• ₹30,000 – ₹50,000 per month• Salary based on experience and expertiseBenefits• Health InsuranceCompany OverviewClove Dental is a leading dental healthcare provider in India, known for its standardized clinical protocols, advanced dental technology, and patient-focused services across multiple locations.FAQsWhat is the employment type?• Full-TimeWhat is the salary range?• ₹30,000 – ₹50,000 per monthIs experience required?• Yes, as per qualification criteriaWhat qualification is required?• BDS (3–4 years experience) or MDS (1–2 years experience)Where is the clinic located?• Tingre Bagar & Dhankawadi, Pune, MaharashtraApplication Tips• Highlight clinical leadership or management experience• Mention experience with dental software and databases• Include Dental Council license details• Emphasize diagnostic and treatment planning expertise

Why This Role MattersThe Associate Dentist supports the delivery of quality dental care in a well-established clinical setup. This role contributes to patient treatment, maintains professional standards, and ensures smooth functioning of dental services during assigned slots.Job DescriptionApollo Clinic is hiring a Part-Time Associate Dentist for its reputed and running dental setup in Viman Nagar, Pune, Maharashtra. The role is ideal for a qualified dentist seeking evening clinical practice opportunities in an established clinic environment.Key Features of the Role• Position: Associate Dentist• Company: Apollo Clinic• Location: Viman Nagar, Pune, Maharashtra• Employment Type: Part-Time• Salary Range: ₹11,847.97 – ₹35,663.65 per month• Work Setting: Dental Clinic• Shift Availability: Evening Slot (Two slots available)Responsibilities• Provide general dental consultation and treatment• Diagnose dental conditions and plan appropriate treatments• Perform routine dental procedures• Maintain patient records and documentation• Follow hygiene and sterilization protocols• Ensure smooth functioning of the dental clinic during assigned hoursRequired Qualification• BDS (Bachelor of Dental Surgery)• Valid State Dental Council RegistrationExperience and Skills• Experience preferred• Strong clinical and diagnostic skills• Good patient-handling and communication skills• Ability to work independently in assigned slotsImportant Remarks• Part-time position• Evening slots available (Two openings)• Salary depends on experience• Immediate resume submission requiredSalary Insights• ₹11,847.97 – ₹35,663.65 per month• Final salary based on experience and clinical expertiseCompany OverviewApollo Clinic is a reputed healthcare provider offering comprehensive medical and dental services, known for its established clinical setup and patient-centered care in Pune.FAQsWhat is the employment type?• Part-TimeWhat is the salary range?• ₹11,847.97 – ₹35,663.65 per monthIs experience required?• PreferredWhat qualification is required?• BDS with valid Dental Council RegistrationWhere is the clinic located?• Viman Nagar, Pune, MaharashtraApplication Tips• Highlight clinical experience and independent practice ability• Mention Dental Council registration details• Specify availability for evening slots• Attach updated resume with relevant experience

Why This Role MattersThe Physiotherapist plays a crucial role in supporting oncology patients through rehabilitation during and after cancer treatment. At MOC Cancer Care & Research Centre, this role focuses on improving mobility, managing pain, enhancing recovery, and promoting overall quality of life for patients undergoing cancer care.Job DescriptionThe Physiotherapist will assess patients, develop individualized treatment plans, and provide rehabilitation support to oncology patients. The role involves managing pain, mobility issues, lymphedema, fatigue, and post-surgical recovery. This is a full-time, permanent position based at the Swargate location in Pune.Key Features of the Role• Position: Physiotherapist – Oncology Rehabilitation• Company: MOC Cancer Care & Research Centre• Location: Swargate, Pune, Maharashtra• Employment Type: Full-Time, Permanent• Salary: ₹30,000 – ₹35,000 per month• Working Days: Monday to Saturday (Sunday Fixed Off)• Duty Hours: 8 Hours per DayResponsibilities• Assess patients and develop individualized physiotherapy treatment plans• Provide rehabilitation support to oncology patients during and after treatment• Manage pain, mobility issues, lymphedema, fatigue, and post-surgical recovery• Monitor patient progress and modify treatment plans as required• Maintain accurate documentation and patient records• Collaborate with oncologists and multidisciplinary healthcare teams• Educate patients and caregivers on home exercise programs and mobility techniquesRequired Qualification• Bachelor’s or Master’s degree in Physiotherapy (BPT/MPT)• Valid professional registrationExperience and Skills• 2–4 years of clinical experience (Oncology experience preferred)• Strong communication and interpersonal skills• Compassionate and patient-centric approach• Ability to work collaboratively within a multidisciplinary teamImportant Remarks• Permanent full-time opportunity• Industry-standard salary based on experience• Exposure to specialized oncology rehabilitationSalary Insights• ₹30,000 – ₹35,000 per month• Additional employee benefits includedEmployee Benefits• Health insurance• Leave encashment• Life insurance• Paid sick time• Provident FundCompany OverviewMOC Cancer Care & Research Centre is a leading oncology healthcare provider dedicated to delivering comprehensive and compassionate cancer treatment services. The organization focuses on multidisciplinary care, advanced treatment protocols, and patient-centered rehabilitation services.FAQsWhat is the employment type?• Full-Time, Permanent.What qualification is required?• BPT or MPT with valid professional registration.Is oncology experience mandatory?• Preferred but not mandatory (2–4 years experience required).What are the working days?• Monday to Saturday (Sunday Fixed Off).Application Tips• Highlight oncology rehabilitation or post-surgical experience• Emphasize communication and patient-care skills• Mention multidisciplinary teamwork experience• Keep CV clear and professionally structured

Why This Role MattersThe Medical and Scientific Reviewer ensures that all promotional and non-promotional materials, scientific documents, and medical communications are accurate, scientifically balanced, and compliant with applicable regulations. By reviewing content across multiple therapeutic areas, interpreting scientific literature, and supporting medical affairs and information teams, this role helps clients deliver high-quality, ethical, and scientifically rigorous information to healthcare professionals and patients. The position ensures both regulatory compliance and medical accuracy, contributing directly to patient safety and informed decision-making.Job DescriptionThe Medical and Scientific Reviewer is responsible for reviewing, fact-checking, and approving scientific and medical content for promotional and non-promotional materials. The role involves analyzing literature, preparing scientifically rigorous documents, supporting medical affairs, and ensuring alignment with medical strategies. The reviewer collaborates with internal teams, clients, and medical signatories, maintaining compliance with regulatory requirements and best practices. This position also contributes to SOP creation, process improvements, and content management using platforms like Veeva Vault PromoMats / MedComms.Key Features Of The Role• Review and fact-check promotional and non-promotional materials for medical, legal, and regulatory compliance• Ensure scientific accuracy, clinical and statistical relevance, and balanced presentation of data• Evaluate claims, references, and alignment with approved product labels• Support medical content creation including SRDs, FAQs, slide decks, abstracts, posters, and training materials• Collaborate with internal and client medical signatory reviewers for timely document approval• Use content management tools (e.g., Veeva Vault PromoMats / MedComms) for document upload, referencing, and annotations• Identify, communicate, and resolve issues impacting timelines or content quality• Propose content and process improvements to reduce recurring errors• Participate in client meetings and contribute to strategic discussions on medical communications• Support SOP, template, checklist, and style guide creation and updatesResponsibilities• Conduct thorough scientific review of medical and promotional content across multiple therapeutic areas• Analyze and interpret scientific literature, clinical trials, and regulatory data• Ensure all content is scientifically accurate, contextually correct, and aligned with medical strategy• Review claims for accuracy, relevance, and adequate supporting data• Collaborate with medical, regulatory, and creative teams to resolve findings and approve content• Support medical affairs and medical information teams with content creation and document development• Ensure compliance with US regulations, industry codes of practice, and internal standards• Manage multiple projects and meet deadlines while maintaining high-quality outputs• Flag quality issues proactively and implement corrective or preventive actions• Support cross-functional collaboration across EVERSANA business units and client teamsRequired QualificationsEducational Requirements• PharmD, M.Pharm, MS Pharm, Ph.D., BDS, MDS, or MBBS with relevant experience in scientific writing or reviewingExperience And Skills• Minimum of 2 years of experience in scientific writing, document QC, or medical content review within life sciences or pharmaceuticals• Experience across multiple therapeutic areas including oncology, immunology, rare diseases, and others• Proficient in literature searches and analysis using PubMed, Ovid, Embase, RightFind, etc.• Strong medical and scientific knowledge, with understanding of clinical trials, drug development, and medical terminology• Experience with content management platforms (e.g., Veeva Vault PromoMats / MedComms)• Excellent communication, editing, and project management skills• High attention to detail, analytical thinking, and ability to translate complex data for different audiences• Knowledge of US regulations and best practices for medical communications and promotional materials• Ability to work independently and collaboratively in a matrix team environmentSalary Insights• Compensation as per company norms and industry standards• Opportunities to work remotely and exposure to global medical communications projects• Career growth in medical affairs, regulatory, and scientific communicationsCompany OverviewEVERSANA is a global life sciences services provider, supporting more than 650 clients with commercialization, medical, regulatory, and scientific services. The company emphasizes diversity, inclusion, and professional development while delivering high-quality medical content to improve patient outcomes. EVERSANA values integrity, collaboration, and scientific excellence across all therapeutic areas.FAQsQ: What type of materials will I review?A: Promotional and non-promotional materials, scientific responses, FAQs, slide sets, abstracts, posters, and medical training materials.Q: Will I interact with clients?A: Yes, the role involves collaboration with internal teams, medical signatory reviewers, and client representatives.Q: What tools are used for content management?A: Veeva Vault PromoMats, MedComms, Microsoft Office, Acrobat, and other content management platforms.Application Tips• Highlight experience in medical or scientific content review across therapeutic areas• Emphasize familiarity with regulatory requirements and industry best practices• Showcase expertise in literature analysis, scientific writing, and document QC• Demonstrate project management, attention to detail, and collaborative skills

Why This Role MattersThe Physiotherapist is essential in supporting oncology patients through rehabilitation during and after cancer treatment. At MOC Cancer Care & Research Centre, this role ensures patient mobility, pain management, and post-surgical recovery, contributing to comprehensive and compassionate cancer care.Job DescriptionThe Physiotherapist will assess oncology patients, develop individualized treatment plans, provide rehabilitation support, monitor progress, and collaborate with the multidisciplinary team. The role also involves patient and caregiver education on home exercises and mobility techniques.Key Features of the Role• Position: Physiotherapist• Company: MOC Cancer Care & Research Centre• Location: Swargate, Pune, Maharashtra, India• Employment Type: Full-Time, Permanent• Salary: ₹30,000 – ₹35,000 per month• Work Environment: Oncology healthcare center• Eligibility: BPT / MPT with professional registrationResponsibilities• Assess patients and develop individualized physiotherapy treatment plans• Provide rehabilitation support for oncology patients• Help manage pain, mobility issues, lymphedema, fatigue, and post-surgical recovery• Monitor patient progress and update treatment plans as required• Maintain accurate patient records and documentation• Collaborate with oncologists and the multidisciplinary team• Educate patients and caregivers on home exercises and mobility techniquesRequired Qualification• Bachelor’s or Master’s degree in Physiotherapy (BPT/MPT)• Valid professional registrationExperience and Skills• 2–4 years of experience; oncology experience preferred• Excellent communication and interpersonal skills• Compassionate, patient-focused, and professional approachImportant Remarks• Full-time, permanent role• Monday to Saturday (Sunday fixed off), 8 hours per day• Benefits include health insurance, life insurance, paid sick time, leave encashment, and provident fundSalary Insights• ₹30,000 – ₹35,000 per monthCompany OverviewMOC Cancer Care & Research Centre is a leading oncology healthcare provider in Pune, committed to delivering comprehensive, evidence-based, and compassionate cancer care, focusing on rehabilitation and holistic patient support.FAQsWhat employment types are available?• Full-time, permanent.What qualification is required?• BPT / MPT with valid registration.Is oncology experience required?• Preferred but not mandatory.What benefits are offered?• Health insurance, life insurance, paid sick time, leave encashment, provident fund.Application Tips• Highlight BPT / MPT qualifications and registration• Emphasize oncology rehabilitation or physiotherapy experience• Showcase patient-focused care and communication skills• Keep CV professional and structured

Why This Role MattersIn the pharmaceutical industry, regulatory compliance is the backbone of product approval and market sustainability. Every medicinal product must meet strict regulatory requirements before it reaches patients. Timely and accurate dossier submissions, effective authority communication, and lifecycle documentation management ensure uninterrupted product availability and protect public health.The Regulatory Affairs Executive plays a crucial role in managing product registrations, renewals, and post-approval variations. This position directly supports business growth by ensuring products remain compliant with evolving regulatory frameworks. By coordinating across departments and maintaining precise documentation, the role ensures smooth regulatory operations throughout the product lifecycle.Job DescriptionWe are hiring a Regulatory Affairs Executive responsible for preparing and submitting regulatory dossiers, managing product registrations, and ensuring compliance with applicable national and international guidelines. The role involves coordination with cross-functional teams, responding to regulatory authority queries, and maintaining regulatory documentation systems.The candidate will be responsible for end-to-end regulatory submission support, including new registrations, renewals, and variations, while ensuring product labeling and packaging compliance. The role requires strong attention to detail, regulatory knowledge, and the ability to manage multiple timelines effectively.Key Features of the Role• End-to-end responsibility for dossier preparation and submission• Exposure to new registrations, renewals, and variations• Coordination with cross-functional departments• Direct handling of regulatory authority queries• Involvement in labeling and artwork compliance review• Lifecycle documentation and database managementResponsibilities• Prepare and submit regulatory dossiers for new product registrations• Manage renewals and post-approval variations in accordance with applicable guidelines• Ensure compliance with national and international regulatory requirements• Coordinate with R&D, Quality Assurance, Manufacturing, and Packaging teams to collect required documentation• Review product labeling, packaging materials, and artworks to ensure regulatory accuracy• Respond to regulatory authority queries within defined timelines• Maintain updated regulatory records, licenses, and submission trackers• Monitor changes in regulatory guidelines and implement necessary updates• Maintain regulatory databases and ensure proper archival of submission documents• Support audits and inspections by providing regulatory documentation• Track submission timelines and ensure timely follow-up with authorities• Assist in preparing regulatory strategy inputs for new product launchesRequired Qualifications• Strong understanding of regulatory submission processes• Knowledge of dossier formats and regulatory documentation requirements• Familiarity with labeling compliance and packaging review• Good knowledge of pharmaceutical regulatory guidelines• Strong documentation management and organizational skills• Ability to work within defined regulatory timelinesEducational Requirements• Bachelor’s degree in Pharmacy (B.Pharm)• Master’s degree in Pharmacy (M.Pharm) preferredEquivalent qualifications in Pharmaceutical Sciences or Life Sciences may also be considered.Experience and Skills• 2–5 years of experience in Regulatory Affairs within the pharmaceutical industry• Experience in preparing and submitting dossiers for registrations, renewals, and variations• Familiarity with regulatory guidelines applicable to domestic and/or export markets• Strong written and verbal communication skills• Ability to coordinate with cross-functional teams effectively• Detail-oriented approach with strong analytical skills• Ability to manage multiple projects and meet strict deadlines• Proficiency in documentation tools and regulatory databasesSalary InsightsAnnual salary range: ₹3,21,000 – ₹4,50,000 per yearCompensation is aligned with industry standards for mid-level regulatory professionals in Pune, Maharashtra. Salary may vary depending on experience level, technical expertise, and exposure to regulatory submissions.Additional Benefits:• Health InsuranceCompany OverviewThe organization operates within the pharmaceutical sector and focuses on regulatory compliance, product registration, and lifecycle management. The company is committed to maintaining high standards of regulatory integrity and ensuring that all products meet applicable guidelines before reaching the market.The work environment promotes cross-functional collaboration, professional development, and continuous regulatory learning to stay aligned with evolving compliance frameworks.FAQs1. Is prior regulatory experience mandatory?Yes, experience in dossier preparation and regulatory submissions is required for this role.2. Does this role involve authority interaction?Yes, responding to regulatory authority queries within defined timelines is a key responsibility.3. Is labeling review part of the job?Yes, reviewing labeling, packaging, and artwork for regulatory compliance is included in the role.4. Is this role limited to domestic submissions?The scope may include domestic as well as export market submissions depending on company requirements.Application Tips• Highlight specific dossiers prepared (new registrations, renewals, variations)• Mention markets handled (India, ROW, etc.)• Emphasize experience in responding to authority queries• Showcase labeling and artwork review expertise• Quantify the number of submissions managed or approvals received• Demonstrate cross-functional coordination experience

Why This Role MattersPreclinical safety studies are essential before any drug progresses to human trials. These studies generate critical data required for regulatory submissions and ensure that pharmaceutical products meet safety standards.This role supports both in-life and terminal phases of safety studies conducted under GLP principles. Accurate documentation, scientific discipline, and regulatory awareness are crucial to maintaining data integrity and compliance. It offers strong foundational exposure for candidates aiming to build careers in toxicology, regulatory affairs, or preclinical research.Job DescriptionThe Research Associate – Toxicology & Safety Studies will assist in regulatory literature searches and support ongoing safety studies in laboratory settings.The position involves maintaining laboratory documentation, assisting in animal handling and dosing procedures, collecting biological samples, and ensuring adherence to SOPs and GLP standards.Key Features of the Role• Support regulatory documentation through literature search• Participation in in-life and terminal study phases• Exposure to GLP-compliant laboratory operations• Hands-on animal handling and dosing experience• Biological sample collection (blood, urine, feces)• Laboratory documentation and quality complianceResponsibilities• Conduct literature searches for regulatory write-ups• Support in-life phase activities of safety studies• Assist in terminal procedures and sample collection• Handle animals as per protocol and GLP standards• Perform dosing procedures under supervision• Collect biological samples accurately• Maintain laboratory worksheets, notebooks, and records• Ensure compliance with written SOPs and GLP principles• Follow quality procedures and documentation practices• Work in coordination with study directors and research teamsRequired QualificationsCandidates must meet the following criteria.Educational Requirements• Graduation in Life Sciences or Pharmacy• Post-Graduation in Life Sciences or Pharmacology preferredExperience and Skills• Understanding of GLP principles• Knowledge of regulatory guidelines (added advantage)• Exposure to laboratory documentation practices• Familiarity with animal handling and dosing techniques• Strong analytical and observational skills• Good interpersonal and communication skills• Result-oriented mindset• Ability to work in structured research environmentsSalary InsightsCompensation will be aligned with industry standards for preclinical research roles and may vary based on qualification and experience.Company OverviewThe organization operates within regulated preclinical research and safety evaluation frameworks, supporting pharmaceutical development through GLP-compliant studies. It maintains high standards of scientific accuracy, documentation integrity, and regulatory compliance.FAQsIs animal handling mandatory?Exposure is preferred, but training may be provided depending on experience.Is GLP knowledge required?Yes, understanding of GLP principles is important.What study phases are involved?Both in-life and terminal phases of safety studies.Is regulatory documentation part of the role?Yes, literature search and regulatory support are included.Are pharmacy graduates eligible?Yes, Life Science and Pharmacy graduates are eligible.Application Tips• Highlight academic projects related to toxicology or pharmacology• Mention GLP training or laboratory certifications• Include any animal handling or dosing experience• Emphasize documentation accuracy and regulatory knowledge• Demonstrate result orientation and teamwork abilities

Why This Role MattersPharmacovigilance professionals handling ICSR QC and Final Review are critical to ensuring accuracy, compliance, and timely regulatory reporting. Their expertise directly impacts patient safety and global drug safety standards.Job DescriptionAn opportunity is open for experienced Pharmacovigilance professionals with 5–7 years of hands-on experience in case processing and ICSR QC/Final Review. The role is based in Pune and is suitable for immediate joiners only.Key Features of the Role:• Location: Pune• Experience: 5–7 years• Domain: Pharmacovigilance• Specialization: ICSR QC / Final Review• Immediate joiners preferred• Freshers are not eligibleResponsibilities• Perform ICSR Quality Control (QC) and Final Medical Review• Ensure compliance with global pharmacovigilance standards• Validate case accuracy, completeness, and regulatory timelines• Review case narratives and coding• Ensure adherence to client SOPs and regulatory requirements• Collaborate with PV teams for case resolutionRequired Qualifications• Degree in Pharmacy, Life Sciences, or related field• 5–7 years of Pharmacovigilance experience• Strong experience in ICSR QC / Final ReviewExperience and Skills:• In-depth knowledge of PV case processing workflow• Understanding of global regulatory guidelines (FDA, EMA, ICH)• Strong analytical and attention-to-detail skills• Experience in safety databases• Good communication and documentation skillsSalary InsightsSalary not disclosed (market-competitive package expected for experienced PV professionals).FAQsQ1 Are freshers eligible?No, only professionals with 5–7 years of relevant experience should apply.Q2 Is case processing experience mandatory?Yes, hands-on experience in ICSR QC/Final Review is required.Q3 What is the location?Pune.Q4 Are immediate joiners preferred?Yes, immediate joiners are preferred.How to ApplyInterested candidates meeting the criteria can share their CV Application Tips• Clearly highlight ICSR QC / Final Review experience• Mention safety databases worked on (e.g., Argus, ARISg)• Specify total Pharmacovigilance experience• Confirm notice period or immediate availability

Why This Role MattersMedical writing plays a central role in translating complex clinical and scientific data into clear, compliant, and impactful communication for healthcare professionals, regulators, and patients. As a Senior Medical Writer at Syneos Health, you will directly support global pharmaceutical and biotech organizations by developing scientifically accurate and regulatory-compliant content. This role contributes to accelerating therapy delivery, enhancing scientific communication quality, and ensuring patient-centric information dissemination. Through high-quality medical information writing, this position strengthens evidence-based decision-making across clinical, regulatory, and medical affairs functions.Job DescriptionThe Senior Medical Writer will serve as a lead contributor on medical information writing projects, supporting global standard scientific response documents, FAQs, guidance materials, manuscripts, and publication deliverables. The role requires coordination with cross-functional teams including data management, regulatory affairs, biostatistics, and medical affairs. The candidate will respond to escalated scientific queries from healthcare professionals and internal stakeholders while ensuring adherence to journal, congress, and company regulatory standards. The position demands scientific accuracy, attention to detail, leadership in mentoring junior writers, and familiarity with literature search and publication planning tools.Key Features of the Role:• Remote full-time opportunity• Leadership role within medical writing function• Exposure to global publication and medical information projects• Cross-functional collaboration with regulatory and clinical teams• Opportunity to mentor junior medical writers• Involvement in scientific figure development and publication planningResponsibilities• Lead assigned medical information writing projects• Mentor and guide less experienced medical writers• Develop and update global scientific response communications (gSSRCs)• Respond to escalated scientific queries from HCPs and stakeholders• Conduct literature searches using PubMed and client databases• Develop manuscripts, abstracts, posters, and oral presentations• Ensure adherence to regulatory and journal guidelines• Review documents for scientific accuracy and referencing quality• Coordinate with regulatory, medical affairs, and biostatistics teams• Support publication planning using tools such as Datavision and PubConnect• Create scientific figures using GraphPad Prism and Adobe Illustrator• Maintain compliance with SOPs and client templates• Monitor project timelines and budget specifications• Serve as peer reviewer for internal document quality checksRequired Qualifications• Strong experience in medical information writing or publication writing• Familiarity with regulatory standards and journal guidelines• Experience handling scientific documentation and literature analysis• Ability to work independently with minimal supervision• Strong project management capabilitiesEducational Requirements:• Advanced degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or related discipline preferred• Equivalent relevant experience consideredExperience and Skills:• Experience in clinical manuscript and publication development• Strong scientific writing and editing expertise• Familiarity with figure creation and data visualization tools• Knowledge of publication planning platforms• Excellent analytical and literature review skills• Strong communication and stakeholder coordination skills• Attention to detail and high-quality documentation standards• Ability to work within budget and timeline constraints• Leadership and mentoring capabilitiesAge Eligibility:No specific age criteria mentioned. Candidates must meet educational and professional qualification requirements.Salary InsightsCompensation is competitive and aligned with industry standards for senior medical writing roles. Salary may vary based on experience, therapeutic expertise, and project leadership exposure. Additional benefits may include career progression programs, training opportunities, and performance incentives.Company OverviewSyneos Health is a fully integrated biopharmaceutical solutions organization operating in over 110 countries with approximately 29,000 employees globally. The organization accelerates clinical development, medical affairs, and commercialization strategies for pharmaceutical and biotech clients. Known for its patient-centric Clinical Development model, Syneos Health supports the majority of recently approved FDA and EMA products. The company promotes diversity, professional growth, and a collaborative culture under its “Work Here Matters Everywhere” philosophy.FAQsIs prior medical writing experience required?Yes, senior-level experience in medical writing is expected.Is the role fully remote?Yes, this position is remote-based in Pune/Pimpri-Chinchwad Area.Does the role involve travel?Minimal travel may be required (less than 25%).What type of documents will be handled?Medical information documents, manuscripts, abstracts, posters, and scientific responses.Are regulatory guidelines important for this role?Yes, adherence to journal, regulatory, and SOP standards is critical.Application Tips• Highlight publication and medical information writing experience clearly• Showcase manuscript, abstract, and scientific communication exposure• Mention familiarity with PubMed, regulatory guidelines, and figure tools• Quantify project leadership or mentoring experience• Emphasize compliance, accuracy, and document quality standards• Tailor your resume to highlight therapeutic area expertise and writing portfolio

Why This Role MattersPharmacovigilance plays a critical role in protecting patient safety by monitoring, detecting, and preventing adverse drug reactions. As a Pharmacovigilance Associate at Tata Consultancy Services, you will contribute directly to global drug safety operations, ensuring regulatory compliance and supporting pharmaceutical clients in maintaining high-quality safety standards. This role is essential in strengthening patient trust, maintaining regulatory integrity, and supporting life sciences innovation through structured safety monitoring and reporting.Job DescriptionTata Consultancy Services is hiring Pharmacovigilance Associates to support adverse event case processing, safety data management, and regulatory compliance activities. The selected candidate will be responsible for reviewing and processing Individual Case Safety Reports (ICSRs), performing drug safety data entry and validation, and ensuring accurate and timely submission of regulatory reports. The role requires hands-on experience with safety databases such as Argus or ARISg and strong knowledge of global pharmacovigilance regulations.Key Features of the Role:• Exposure to global pharmacovigilance operations• Opportunity to work with leading pharmaceutical clients• Hands-on experience with Argus Safety and ARISg databases• Involvement in signal detection and risk assessment support• Cross-functional collaboration within life sciences teams• Competitive salary structure aligned with industry standardsResponsibilities• Process and review adverse event case reports• Perform drug safety data entry and validation• Ensure compliance with global pharmacovigilance regulations• Work on safety databases such as Argus or ARISg• Conduct case follow-ups and resolve safety queries• Prepare and review case narratives• Maintain accuracy and completeness of safety data• Collaborate with cross-functional teams for safety reporting• Support signal detection and risk assessment activities• Participate in audits and regulatory inspections• Maintain documentation as per SOPs and guidelines• Ensure timely submission of regulatory reports• Identify discrepancies and resolve safety data issues• Assist in quality control and compliance checksRequired Qualifications• University Graduate (Life Sciences, Pharmacy, Biotechnology, Nursing, or related field preferred)• 2–4 years of experience in pharmacovigilance or drug safety• Experience in ICSR processing and case management• Hands-on knowledge of Argus Safety or ARISgEducational Requirements:• Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, or related discipline• Relevant certification in Pharmacovigilance preferredExperience and Skills:• Strong understanding of pharmacovigilance and drug safety processes• Expertise in ICSR case processing• Knowledge of global regulatory compliance requirements• Proficiency in Argus Safety or ARISg• Good understanding of medical terminology• Strong analytical and data review skills• Attention to detail and quality-focused mindset• Effective communication and documentation skills• Ability to work within defined timelines and SOP frameworksAge Eligibility:No specific age criteria mentioned. Candidates must meet educational and experience requirements.Salary Insights₹4,00,000 – ₹8,00,000 per annum (based on experience and expertise). Compensation may vary depending on candidate profile, project allocation, and skill level.Company OverviewTata Consultancy Services (TCS) is a global IT services, consulting, and business solutions organization delivering technology-driven solutions to leading enterprises worldwide. With a strong presence in life sciences and healthcare domains, TCS supports pharmaceutical and biotech organizations in pharmacovigilance, regulatory operations, clinical research, and digital transformation initiatives. TCS operates across multiple countries and is known for innovation, operational excellence, and client-centric solutions.FAQs1. Is experience in Argus mandatory?Experience in Argus or ARISg is strongly preferred.2. Is this a client-facing role?The role involves collaboration with internal and external stakeholders in safety reporting.3. Is remote work available?Location is specified as Mumbai / Pune; work model depends on project allocation.4. What growth opportunities are available?Career progression may include Senior PV Associate, Drug Safety Specialist, or Quality Reviewer roles.Application Tips• Highlight ICSR processing and case narrative experience clearly• Mention safety database expertise (Argus/ARISg) prominently• Showcase knowledge of global PV regulations• Quantify case volume handled per month if possible• Emphasize audit experience and compliance adherence• Tailor your CV specifically for pharmacovigilance keywords

Role & Responsibilities• Perform primary medical review of safety cases including assessment of seriousness, listedness/labeling, causality, adverse event coding, and narrative review• Update and document daily case data and feedback in tracking tools to ensure workflow management• Take full responsibility for assigned deliverables in line with quality, compliance, productivity SLAs, and KPIs• Provide medical training and guidance to case processing teams after completion of one year of tenure• Support aggregate reporting and signal detection activities related to single case processing• Maintain high standards of customer service and compliance cultureQualification• Bachelor’s degree in Medical Science or MD or DO or equivalent qualification• Fortrea may consider relevant equivalent experience in lieu of formal education• English proficiency – Speaking (ILR Level 3+), Writing/Reading (ILR Level 4+)Experience• Working knowledge of medical sciences, diagnosis, therapeutics, drug treatments, and procedures• Knowledge of regulatory requirements for Clinical Research• Understanding of ICH-GCP guidelines• 1–2 years of clinical practice experience preferredSkills• Medical safety and pharmacovigilance knowledge• Clinical case assessment and causality evaluation• Understanding of regulatory compliance and post-marketing surveillance• Strong documentation and analytical skills• Ability to work in office or home-based environmentAbout the CompanyFortrea is a global contract research organization (CRO) providing clinical development and post-marketing services to pharmaceutical, biotechnology, and medical device companies. The organization focuses on delivering high-quality clinical research, pharmacovigilance, and regulatory support services to improve patient safety and accelerate drug development worldwide.