Doctor Jobs

Roles & Responsibilities• Conduct patient assessments and provide dental care• Diagnose oral health conditions and create treatment plans• Perform routine dental procedures including fillings, cleanings, and extractions• Maintain accurate medical records and documentation• Use appropriate medical terminology in all patient communications and documentation• Ensure adherence to hygiene, safety, and clinical protocols• Collaborate with dental team to provide patient-centered careSkills Required• Proficiency in patient assessment, medical documentation, and record-keeping• Strong understanding of dental procedures and treatment planning• Excellent communication and interpersonal skills• Ability to work effectively in a team environmentQualifications• Bachelor’s degree in Dentistry (BDS) from a recognized institution• Valid dental license to practice• Minimum 1 year of clinical experience preferredAbout the CompanyDrSmilez Healthcare Pvt Ltd operates a network of dental centers in Chennai, providing comprehensive dental care services. The organization is committed to patient-centered care, high-quality treatments, and professional development for its dental staff. DrSmilez focuses on delivering exceptional oral healthcare while maintaining modern facilities and advanced treatment protocols.

Roles & Responsibilities• Provide primary healthcare services under the Suitcase Clinic model• Conduct consultations, urgent care, diagnostic testing, and treatment across domains such as Dental, Pediatrics, Geriatrics, and Gynaecology• Manage patient interactions and deliver high-quality, patient-centered care• Prescribe medications and develop treatment plans• Maintain accurate medical records using AI-powered tools• Collaborate with the healthcare team to improve patient outcomes• Utilize AI-driven tools for scheduling, record-keeping, and diagnostics to ensure seamless patient experiences• Attend to patients at various locations across Pune as requiredSkills Required• Proficiency in patient care, diagnosis, and treatment planning for diverse primary healthcare needs• Strong communication and interpersonal skills for patient consultations and team collaboration• Ability to work flexibly and attend patients in multiple onsite locations• Experience or willingness to work with AI-driven clinical tools• Prior experience in community healthcare or portable clinical setups is a plusQualifications• MD Pediatrics, MD Medicine, MBBS with experience in Geriatrics, Gynecologist, or Dentist• Relevant medical licensure and certifications to practice in IndiaWhat We Offer• Opportunity to work in an innovative AI-integrated healthcare setup• Exposure to diverse patient populations across age groups and specialties• Supportive and collaborative work environment• Hands-on experience with portable, tech-enabled primary healthcare delivery• Opportunities for professional growth and skill developmentAbout the CompanyHAI Suitcase Clinics®, a unit of Yuvrus Healthcare Innovations, is revolutionizing primary healthcare delivery by combining portable medical services with advanced AI technology. Based in Pune, the clinic brings high-quality care directly to patients, whether at home or in a clinic, across Dental, Pediatrics, Gynaecology, and Geriatrics. By integrating smart automation, digital prescriptions, real-time scheduling, and secure medical record management, HAI Suitcase Clinics ensures efficient, accessible, and patient-centered healthcare anytime, anywhere.

Roles & Responsibilities• Diagnose, treat, and manage oral and dental health issues• Perform dental procedures including preventive, restorative, and surgical treatments• Provide guidance and education to patients on oral health and hygiene• Maintain accurate and detailed patient records• Collaborate with other healthcare professionals for integrated patient care• Provide training and guidance to junior staff and team members• Ensure patient-focused care with high standards of quality and safetySkills Required• Strong diagnostic and clinical skills in dentistry• Knowledge of medicine and emergency medicine practices• Familiarity with cardiology and related conditions is an advantage• Excellent communication and interpersonal abilities• Ability to train, mentor, and work collaboratively with staffQualifications• Bachelor’s degree in Dentistry (BDS) or equivalent• Required licensure to practice dentistry• Specialization or prior experience in dental surgery is a plusExperience• Demonstrated experience working in a clinical or hospital setting• Experience collaborating with physicians and healthcare teamsAbout the CompanyZeel Hospital is a healthcare facility in Sagwara, Rajasthan, dedicated to providing comprehensive and patient-centered medical and dental services. The hospital combines modern facilities, skilled healthcare professionals, and a focus on quality care to ensure optimal outcomes for patients. Zeel Hospital emphasizes compassionate treatment, teamwork, and the promotion of overall health and wellness within the community.

Roles & Responsibilities• Diagnose and treat conditions related to the face, mouth, and jaws• Perform oral surgeries, including extractions of wisdom, normal, and complex teeth• Conduct dental implant procedures• Ensure strict adherence to medical, safety, and sterilization protocols• Manage patient care with high standards of quality and safety• Collaborate effectively with the dental and clinical team for comprehensive careSkills Required• Expertise in oral surgery and dental implants• Strong diagnostic, decision-making, and patient management skills• Knowledge of anesthesiology relevant to oral and maxillofacial procedures• Excellent communication and teamwork abilities• Commitment to patient safety and continuous learningQualifications• Board certification in Oral and Maxillofacial Surgery• Strong foundation in medicine and dentistry with focus on oral health careExperience• Proven experience in oral and maxillofacial surgical proceduresAbout the CompanyN Patel Dental Care is a primary dental clinic located in central Pune, committed to delivering high-quality, patient-centered dental care. The clinic combines experienced dental professionals with modern surgical and diagnostic protocols, emphasizing safety, precision, and compassionate care to ensure optimal outcomes for all patients.

Roles & Responsibilities:• Provide quality healthcare services as per assigned medical or paramedical role• Diagnose, treat, and manage patients following NHM clinical guidelines• Deliver nursing care, patient monitoring, and community health support• Perform dental, pharmacy, and laboratory services accurately and efficiently• Maintain patient records, reports, and documentation• Support public health programs and outreach initiatives• Ensure hygiene, safety standards, and proper equipment handling• Coordinate with healthcare teams and government health officials• Follow ethical practices and organizational protocolsQualification:• Medical Officer – MBBS• Community Nurse – GNM / B.Sc Nursing• Dental Technician – BDS• Lab Technician – 12th / DMLT• Other posts – As per official notificationExperience / Age Limit:• Minimum Age: 21 Years• Maximum Age: 45 Years• Age relaxation applicable as per Government normsSelection Process:• InterviewApplication Fee:• General / Other Candidates – ₹100/-• SC / ST / OBC Candidates – ₹50/-Important Dates:• Application Start Date: 19-01-2026• Application Last Date: 09-02-2026About the Company:The District Health and Family Welfare Society (DHFWS), Darjeeling operates under the National Health Mission (NHM) to strengthen public healthcare delivery across the district. The organization focuses on providing accessible, affordable, and quality healthcare services through hospitals, community health centers, and outreach programs, aiming to improve overall health outcomes and support government public health initiatives.Official NotificationClick Here

Roles & Responsibilities:• Assist in planning and execution of research activities under assigned projects• Conduct clinical, laboratory, and field-based research work as required• Collect, analyze, and document research data accurately• Support interdisciplinary research initiatives related to animal and public health• Prepare reports, presentations, and research documentation• Coordinate with research teams and project investigators• Ensure compliance with institutional research protocols and ethical standards• Maintain proper records of research activities and project outcomesTotal Vacancy: 01Qualification:• MBBS / BDS from a recognized institutionExperience / Age Limit:• Minimum Age: 21 Years• Maximum Age: 45 Years• Age relaxation applicable as per organizational normsSelection Process:• InterviewImportant Dates:• Walk-in Start Date: 21-01-2026• Walk-in Last Date: 27-01-2026Walk-in Interview Address:• Office of the Director, Centre for One Health, GADVASU, LudhianaAbout the Company:Guru Angad Dev Veterinary and Animal Sciences University (GADVASU), under the Department of Animal Husbandry and Dairying, is a premier institution dedicated to education, research, and extension services in veterinary, animal, and allied sciences. The university plays a key role in advancing animal health, zoonotic disease research, and public health initiatives through interdisciplinary and translational research programs.Official NotificationClick Here

Total Vacancies: 23Roles & Responsibilities:• Provide medical, dental, nursing, and allied healthcare services as per assigned role• Diagnose, treat, and manage patients in accordance with ECHS healthcare protocols• Maintain accurate medical records and patient documentation• Assist senior medical professionals in delivering quality healthcare services• Ensure compliance with hygiene, safety, and government healthcare standards• Perform administrative and support duties related to healthcare operations• Carry out duties responsibly as per designation (Medical, Paramedical, Technical, or Support Staff)Qualification:• Medical Officer: MBBS• Dental Officer: BDS• Nursing Assistant: GNM / B.Sc Nursing• Other Posts: 8th / 12th (as per post)Experience / Age Limit:• Minimum Age: 21 Years• Maximum Age: 45 Years• Age relaxation applicable as per ECHS / Government normsSelection Process:• InterviewImportant Dates:• Application Start Date: 22-01-2026• Last Date to Apply: 12-02-2026About the Company:The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative established to provide comprehensive medical care to ex-servicemen and their dependents. ECHS operates through a wide network of polyclinics and empanelled hospitals across the country, ensuring accessible, affordable, and quality healthcare services. The organization plays a vital role in supporting the health and well-being of veterans by delivering reliable and structured medical assistance under government healthcare standards.Official NotificationClick Here

Roles & Responsibilities • Create and maintain Safety Data Sheets (SDS) for global markets • Perform hazard classification as per GHS, CLP, OSHA regulations • Handle regulatory compliance workflows including labels, registrations, renewals • Review raw materials, formulations, and finished products for compliance • Maintain regulatory data accuracy in SDS authoring tools and ERP systems • Respond to regulatory queries from internal and external stakeholders • Ensure documentation and records meet regulatory standards and timelines Qualification • Bachelor’s or Master’s degree in Chemistry, Pharmacy, Chemical Engineering, or related field Experience • Experience in corporate regulatory affairs or chemical regulatory environment • Hands-on exposure to SDS and label authoring • Experience in product registration or regulatory compliance preferred Skills • Strong knowledge of global chemical regulations (GHS, CLP, OSHA) • SDS and label authoring experience • Good analytical, documentation, and communication skills • Ability to work independently and with cross-functional teams About the Organisation Diversey, a Solenis company, is a global leader in hygiene and cleaning solutions. Its Global Regulatory Affairs Service Center (GRASC) in Mumbai supports worldwide regulatory compliance across Diversey’s chemical product portfolio, offering strong global exposure and professional growth.

Roles & Responsibilities • Handle regulatory compliance workflows including SDS creation, labels, product registrations, notifications, and renewals • Author Safety Data Sheets (SDS) for multiple global geographies as per applicable regulations • Derive hazard classifications for substances and mixtures using GHS, CLP, OSHA, and other regulations • Perform raw material, formulation, and finished product compliance reviews • Maintain data accuracy and integrity in SDS authoring tools and ERP systems • Respond to regulatory queries from internal and external stakeholders within defined TATs • Coordinate with team leads and SMEs for resolution of complex or high-priority requests • Maintain regulatory records as per defined formats and standards • Support global regulatory compliance across Diversey’s product portfolios Qualification • Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, Environmental Science, Pharmacy, or related discipline Experience • Experience working in a corporate regulatory affairs or chemical regulatory environment • Hands-on experience in SDS and label authoring • Exposure to product registration, regulatory compliance, or regulatory consulting • Proven interaction with competent authorities is preferred Skills • Strong knowledge of global chemical regulations and hazard communication (GHS, CLP, OSHA) • Experience with SDS authoring software and regulatory databases • Good analytical, documentation, and problem-solving skills • Ability to prioritize tasks and meet strict timelines • Excellent written and verbal communication skills in English • Ability to work independently and in cross-functional teams About the Organisation Diversey, a Solenis company, is a global leader in hygiene, cleaning, and sustainability solutions. Through its Global Regulatory Affairs Service Center (GRASC) in Mumbai, Diversey supports regulatory compliance across worldwide markets. Solenis values its people as its greatest asset, offering a collaborative, inclusive, and growth-oriented work environment with exposure to global regulatory operations.

Roles & Responsibilities • Perform plant troubleshooting and process optimization in coordination with Production teams • Investigate and close OOS/OOT cases; execute DOE and implement CAPA • Develop and implement salvage processes for non-conforming batches • Prepare and submit PDRs and technical reports to QA • Participate in Plant CFT meetings and provide technical inputs • Conduct laboratory trials to resolve plant issues and share technical data • Ensure documentation compliance with GLP, GMP, and cGMP guidelines • Participate in continuous training, safety programs, and technical skill development Qualification • M.Sc in Chemistry / Pharmaceutical Sciences or related discipline Experience • 1–3 years of experience in Process Technology / Manufacturing / Technical Services • Exposure to pharmaceutical plant operations preferred Skills • Strong knowledge of GMP, cGMP, and GLP requirements • Hands-on experience with OOS/OOT investigations, DOE, and CAPA • Good documentation and report-writing skills • Strong analytical and problem-solving abilities • Effective communication and cross-functional coordination skills About the Organisation Cadila Pharmaceuticals is one of India’s leading pharmaceutical manufacturers with a strong presence across domestic and international markets. Known for its focus on quality, innovation, and patient-centric solutions, Cadila offers robust opportunities for professionals to grow in pharmaceutical manufacturing, process technology, and GMP-driven operations through hands-on exposure and cross-functional collaboration.

Roles & Responsibilities • Search and retrieve toxicological data from scientific literature and regulatory databases to support safety assessment of new and existing products • Review and document safety data for ingredients, products, and technologies used in consumer healthcare products • Prepare toxicology sections of Ingredient Monographs, safety statements, and product summaries • Summarize and interpret risk assessment data for key toxicological endpoints • Identify, analyze, and report project-relevant data from secondary sources and available databases • Respond to safety-related queries from consumers and regulatory authorities • Ensure accuracy, relevance, and up-to-date toxicological information in all deliverables • Work independently as well as collaboratively within project-specific teams Qualification • Master’s degree in Toxicology, Life Sciences, Pharmacy, or a related scientific discipline Experience • 1–2 years of experience in toxicological research, safety assessment, or scientific documentation Skills • Strong domain knowledge in Toxicology • Experience with regulatory and scientific databases (ECHA, PCPC, EFSA, ToxPlanet, Embase, PubMed, etc.) • Excellent scientific writing and report preparation skills • Strong analytical and data interpretation abilities • Proficiency in MS Office (PowerPoint, basic Excel) and internet research tools • Good written and verbal communication skills • Ability to work independently in a fast-paced environment About the OrganisationThe organization is a globally reputed pharmaceutical company committed to ensuring the safety of its products through robust toxicological evaluation and scientific excellence. It offers a dynamic, performance-driven environment with opportunities for learning, professional growth, and exposure to global product safety operations. 

Roles & Responsibilities Literature Review & Evidence Generation • Conduct systematic and targeted literature searches (PubMed, Embase, Cochrane, open sources) • Analyze clinical and scientific data to generate meaningful insights • Stay updated on therapeutic, regulatory, and guideline developments Medical & Scientific Writing • Create, review, and edit scientific content across OTC and Rx domains • Develop manuscripts, abstracts, posters, slide decks, guideline summaries, and white papers • Ensure compliance with publication and ethical standards (ICMJE, CONSORT) Content Review & Quality Control • Review medical, promotional, and scientific materials as per SOPs and guidelines • Validate references, ensure plagiarism-free content, and maintain formatting standards • Ensure clarity, accuracy, and consistency in all deliverables Project Execution & Collaboration • Understand client objectives and timelines and deliver high-quality outputs • Manage multiple projects simultaneously and respond to ad-hoc requests • Collaborate with cross-functional teams including medical writers, graphics, and clients Qualification • MBBS / BDS / PhD / Master’s in Pharmacy or related fieldSkills • Strong scientific writing, editing, and literature analysis skills • Excellent knowledge of clinical study designs and evidence synthesis • Proficiency in MS Word, PowerPoint, Excel, and online research tools • Strong attention to detail, time management, and independent working ability • Excellent written and verbal communication skills Good to Have • Exposure to US/EU regulatory documentation • Experience with reference management tools (EndNote, Zotero, Mendeley) • Familiarity with statistical or visualization tools (SPSS, RevMan, GraphPad, R) About the Organisation A global scientific communications organization supporting pharmaceutical, OTC, and consumer healthcare clients with high-quality medical writing, evidence synthesis, and compliant scientific content across therapeutic areas.

Roles & Responsibilities • Develop and maintain pharmaceutical forecasting models across multiple therapeutic areas • Support portfolio strategy and valuation decisions in collaboration with BD Analytics HOCT team • Apply statistical forecasting, time-series analysis, and predictive modeling techniques • Perform scenario analysis related to pricing, market access, and regulatory outcomes • Analyze large datasets including sales forecasts, epidemiology, and competitive intelligence • Build advanced Excel-based forecasting and financial models, including dashboards • Prepare insight-driven reports and PowerPoint presentations for senior leadership • Collaborate with cross-functional and IT teams to automate data collection and reporting • Monitor market trends, competitor activity, and pipeline developments Qualification • Bachelor’s or Master’s degree in Biology, Biotechnology, Finance, Economics, Business, or related field • MBA preferred but not mandatory Experience • 1–3 years of experience in pharmaceutical forecasting, portfolio analytics, or commercial analytics • Prior exposure to Oncology, Hematology, or Cell Therapy is an added advantage Skills • Strong proficiency in Advanced Excel and VBA • Experience handling pharma datasets (sales, epidemiology, competitive intelligence) • Knowledge of forecasting methodologies and analytical modeling • Exposure to BI tools, forecasting software, or Python is a plus • Strong analytical, problem-solving, and critical-thinking skills • Excellent communication and stakeholder management abilities • Ability to work independently and collaborate across teams About the Organisation Bristol Myers Squibb (BMS) is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for patients with serious diseases. With a strong presence in Oncology, Hematology, and Cell Therapy, BMS leverages advanced analytics and data-driven decision-making to shape portfolio strategy and drive impactful business outcomes worldwide.

Roles & Responsibilities • Manage day-to-day administrative activities for non-linguistic pharmacovigilance projects • Coordinate file transfers, internal quality checks, and client deliveries • Track project progress and ensure adherence to timelines and deadlines • Support PV production teams to deliver high-quality outputs • Implement and maintain Good Pharmacovigilance Practices (GVP) • Ensure compliance with Good Documentation Practice (GDP) • Provide project support activities as assigned by the supervisor or manager Qualification • Bachelor’s degree (Life Sciences, Pharmacy, or related field preferred) Experience • Fresh graduates or candidates with relevant exposure to pharmacovigilance, literature monitoring, or PV operations • Strong interest in pharmacovigilance and drug safety domain Skills • Excellent written and spoken English communication skills • Proficiency in MS Word, Excel, and Outlook • Strong attention to detail and documentation accuracy • Ability to learn and adapt to PV systems and technology platforms • Good problem-solving and critical-thinking abilities • Strong organizational and multitasking skills • Ability to work independently and in a team-oriented environment About the Organisation TransPerfect is a global leader in language, content, and life sciences solutions, supporting pharmaceutical and biotech companies worldwide. Its Pharmacovigilance Solutions team delivers high-quality, compliant safety services, offering professionals a structured work environment, global exposure, and long-term career growth in the drug safety and pharmacovigilance domain.

Roles & Responsibilities • Manage clinical trial databases ensuring accurate and high-quality data flow • Perform data review, cleaning, and validation activities • Design, develop, and review eCase Report Forms (eCRFs) • Ensure compliance with ICH-GCP, ICH, EU, and FDA regulatory guidelines • Support study start-up, maintenance, and close-out activities • Collaborate with cross-functional teams to maintain data integrity • Contribute to audit readiness and regulatory inspection support • Maintain proper documentation throughout the clinical trial lifecycle Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related scientific discipline Experience • Minimum 1 year of experience as a Clinical Data Manager or Data Management Associate • Equivalent combination of education, training, and experience may be considered Skills • Strong knowledge of clinical data management processes • Understanding of end-to-end clinical trial lifecycle • Hands-on experience with clinical trial databases and CDMS tools • Sound knowledge of ICH-GCP and global regulatory requirements • Excellent documentation, communication, and coordination skills • Fluent in English (written and spoken) • Ability to work collaboratively in cross-functional teams About the Organisation Excelya is a fast-growing, global Contract Research Organization (CRO) known for its people-centric culture and strong presence in Europe and India. The company supports global clinical trials in regulatory-compliant environments, offering professionals long-term career growth, exposure to international studies, hybrid work flexibility, and continuous learning opportunities within a collaborative and inclusive workplace.

Roles & Responsibilities • Maintain thorough knowledge of Pharmacovigilance and Medical Information procedures, legal requirements, and quality documents • Handle adverse event reports and PV data in line with local regulations and company standards • Provide accurate and timely safety information to Health Authorities and relevant stakeholders • Support the Country Safety Head in local safety surveillance, risk management, and safety issue handling • Manage product alerts and market research programs with appropriate regulatory communication • Respond to Medical Information inquiries from healthcare professionals, patients, and customers with high-quality, compliant responses • Collaborate effectively with internal teams and external third parties within PV and Medical Information functions • Actively contribute to North Europe Cluster PV & Medical Information projects and daily operations Qualification • University degree in Pharmacy, Medicine, or an equivalent scientific discipline Experience • Prior experience in the pharmaceutical industry or equivalent • Experience in Pharmacovigilance, Drug Safety, or Medical Information preferred Skills • Strong knowledge of pharmacovigilance regulations and medical information processes • Excellent planning, organization, and attention-to-detail skills • High accuracy and compliance-oriented work approach • Strong interpersonal and communication skills for interaction with HCPs, patients, and internal teams • Proficiency in MS Office and relevant safety/MI systems • Ability to work collaboratively in cross-functional and multicultural teams • Fluency in English and Norwegian (written and spoken) About the Organisation Sanofi is an R&D-driven, AI-powered global biopharmaceutical company dedicated to improving lives through innovative medicines and vaccines. With deep expertise in immunology and a strong pipeline across diabetes, transplant, cardiovascular, and specialty care, Sanofi delivers treatments to more than 100 million people annually, combining global scale with local impact and a strong culture of collaboration, inclusion, and scientific excellence.

Roles & Responsibilities • Develop, program, validate, and maintain clinical trial databases in compliance with company SOPs and regulatory standards • Design and maintain CDASH-compliant Case Report Forms (CRFs) and support the standard CRF library • Perform Medidata RAVE study build activities including database setup, edit checks, and custom functions • Develop and implement custom functions using C# programming within Medidata RAVE • Act as the primary technical point of contact for Data Management teams on assigned clinical studies • Ensure high-quality database design, validation documentation, and audit readiness • Provide technical support throughout the clinical trial lifecycle from study startup to database lock • Support global clinical trials across multiple therapeutic areas Qualification • Bachelor’s or Advanced degree in Life Sciences, Computer Science, or equivalent Experience • Minimum 3+ years of experience in Clinical Database Programming • Hands-on experience in Medidata RAVE study build and maintenance • Experience working in CRO, pharma, or biotech clinical research environments Skills • Strong expertise in Medidata RAVE (study build, edit checks, custom functions) • Proficiency in Custom Functions and C# programming • Knowledge of CDASH standards and CRF design principles • Familiarity with Veeva EDC is an added advantage • Understanding of clinical data management and regulatory requirements • Excellent documentation and validation skills • Strong attention to detail and quality mindset • Effective communication and cross-functional collaboration skills About the Organisation Medpace is a globally recognized Clinical Research Organization (CRO) with more than three decades of experience supporting Phase I–IV clinical trials across multiple therapeutic areas. Known for its scientific-driven approach and strong in-house expertise, Medpace offers a stable, growth-oriented environment where clinical research professionals can build long-term careers while contributing to global drug development programs.

Roles & Responsibilities • Analyze organizational processes, business models, and system integrations with technology • Act as Subject Matter Expert (SME) in Drug Safety and Pharmacovigilance for Veeva Vault Safety • Lead requirement-gathering workshops and define system requirements for Veeva Vault implementation • Assess current-state processes and define future-state business solutions aligned with regulatory needs • Design and configure Veeva Vault to meet FDA, EMA, and ICH regulatory requirements • Document business and system requirements including URS, FS, and user stories • Develop test scripts and support system validation and UAT activities • Serve as the primary liaison between customers, stakeholders, and delivery teams • Collaborate with Product Owners to manage backlogs, prioritize user stories, and support agile delivery • Participate in RFPs and support business development initiatives • Ensure compliance with global Drug Safety and Pharmacovigilance regulations • Provide post-implementation support and optimization for Veeva Vault Safety solutions • Lead change management activities to support client transition to Veeva Vault • Define deployment strategies and post–go-live support plans • Mentor and guide cross-functional teams to ensure successful project delivery Qualification • 15 years of full-time education (Bachelor’s degree or equivalent) Experience • Minimum 5 years of experience in Business Requirements Analysis • Hands-on experience as a Life Sciences / Pharmacovigilance Business Analyst • Experience working on Drug Safety and Pharmacovigilance systems preferred Skills • Strong expertise in Business Requirements Analysis • In-depth knowledge of Pharmacovigilance & Drug Safety Surveillance • Hands-on experience with Veeva Vault Safety • Familiarity with PV systems such as Argus, ArisGlobal • Knowledge of GxP, ICH, FDA, EMA, and global safety regulations (ICH E2E) • Understanding of medical terminology and safety dictionaries (MedDRA, WHO Drug) • Experience with Agile delivery models and backlog management • Proficiency in tools such as JIRA, Confluence, HP-ALM, Q-Test • Working knowledge of SQL, Oracle, XML, Medidata, TMF, eCRF • Strong documentation, communication, and stakeholder management skills • Leadership, mentoring, and cross-functional collaboration abilities • Strong analytical, critical thinking, and problem-solving skills About the Organisation The organization operates at the intersection of life sciences and digital transformation, delivering technology-enabled solutions for Pharmacovigilance, Drug Safety, and regulatory compliance. With a strong focus on Veeva Vault implementations and global regulatory standards, it supports pharmaceutical and life sciences clients in optimizing safety operations, ensuring compliance, and driving efficient, high-quality system delivery across global programs.

Roles & Responsibilities:• Convert patient health information into accurate alphanumeric medical codes• Review medical reports including diagnosis, procedures, and prescriptions• Assign ICD-10, CPT, and HCPCS codes as per medical documentation• Ensure accuracy and compliance with medical coding guidelines• Support medical claims processing and healthcare documentation• Maintain confidentiality of patient and medical recordsQualifications & Experience:• UG / PG graduates from Life Science, Paramedical, or Medical background• Eligible streams include BDS, BPT, Nursing (GNM/DGNM), Pharmacy, Physiotherapy, Biotechnology, Microbiology, Biochemistry, Biomedical, Bioinformatics, Zoology, Botany, Biology, Medical Lab Technology, Radiology, Dialysis, Cardiac Care, OT & Anaesthesia Technology, Physician Assistant, and related courses• Freshers and recent pass-outs (2016–2025) are eligibleSkills Required:• Basic knowledge of Anatomy and Physiology• Good communication and interpersonal skills• Basic computer and documentation skills• Willingness to learn medical coding standards• Attention to detail and accuracyBenefits & Perks:• System-based desk job• 5-day work week (Saturday & Sunday off)• Day shift only• Food and cab facility provided• Performance-based incentives• Salary increment after 6 months for experienced candidates• PF and medical insurance benefits• Gratuity after 5 years• Referral bonus available• Overseas job opportunitiesJob Locations:• Chennai, Coimbatore, Vellore, Trichy, Salem, Erode, Thanjavur• Tirunelveli, Nagercoil, Villupuram, Karur, Theni• Tirupati, Andhra Pradesh, Telangana, Kerala, Tamil NaduAbout the Company:• Achievers Spot is an ISO 9001:2015 certified medical coding training and placement organization based in Chennai.• The company provides classroom and certification-based training in ICD-10, CPT, HCPCS, Anatomy, Physiology, and Medical Coding.• Achievers Spot has successfully placed candidates in leading healthcare BPOs and MNCs across India, offering strong career growth in the healthcare IT sector.