Pharma, Clinical Research & Healthcare Jobs in India
511 open roles from pharma companies, CROs and hospitals, with new openings added most days. Apply directly through each employer's own page or contact.
Showing 151–175 of 249 jobs
Associate Manager - Automation
Pfizer
Visakhapatnam5+ Years · Onsite25 SeptPfizer’s Vizag manufacturing site plays a critical role in producing essential medicines for global markets, and this Associate Manager – Automation position sits at the heart of its digital manufacturing strategy. You will own Emerson DeltaV DCS configuration, instrumentation reliability, and lifecycle support, ensuring that production lines operate safely, compliantly, and without interruption. As Pfizer continues to invest in smart factories, automation engineers who can bridge control systems, field instrumentation, and GMP requirements are increasingly valuable. This role offers exposure to large-scale pharma operations, validation, cybersecurity, and continuous improvement. It is an excellent opportunity for an experienced automation professional to deepen domain expertise, work with cross-functional teams, and contribute directly to accelerating patient access to life-changing therapies.
Access Field Manager – Market Access & Public Health Partnerships
Novartis
Mumbai5+ Years · Onsite25 SeptNovartis is seeking an Access Field Manager to anchor its state-level market access strategy across priority Indian states and Union Territories. Sitting at the intersection of public health, health economics and commercial strategy, this role is central to Novartis's ambition of expanding timely, reimbursed patient access to its innovative therapy portfolio — spanning cardiovascular, oncology, immunology and rare disease. The position matters because India's access landscape is fragmented: each state operates distinct reimbursement pathways, tender mechanisms and public health priorities. By co-creating solutions with government institutions, payers and health administrators, the Access Field Manager directly influences whether patients actually receive the therapies Novartis develops. For experienced market access or public health professionals, this is a rare opportunity to shape health system policy, build durable government partnerships and translate scientific innovation into measurable real-world patient outcomes.
Operational Pricing Lead - WEMEA
Amgen
Hyderabad5+ Years · Onsite25 SeptThis Operational Pricing Lead (WEMEA) role at Amgen is a strategic market access and health economics position based in Hyderabad, supporting West Europe, Middle East, and Africa. The role sits within Amgen's Global Operational Pricing team, a critical function that balances patient access, reimbursement, and commercial sustainability for innovative medicines and a robust biosimilars portfolio. As biosimilar competition and loss-of-exclusivity pressures reshape oncology and inflammation markets, precise pricing strategy becomes central to Amgen's ability to fund innovation and reach more patients. The OPL ensures pricing governance, reference pricing analysis, launch sequencing, and financial planning assumptions are accurate, compliant, and commercially sound. This is a compelling opportunity for finance, consulting, or pharma pricing professionals to influence high-stakes access decisions across diverse markets, work with global affiliates, and build expertise in HTA, reimbursement, and pharmaceutical pricing operations.
Scientist – Research Computational Biology
Amgen
Hyderabad5+ Years · Onsite25 SeptAmgen's ARIA Computational Biology team in Hyderabad sits at the intersection of large-scale data science and disease biology, and this Scientist role is central to how the company replenishes its therapeutic pipeline. Rather than supporting discovery from the periphery, the position directly shapes which targets advance into Amgen's oncology, inflammation and immunology portfolios. The scientist mines multi-modal omics and screening data to characterise disease endotypes, test therapeutic hypotheses and surface novel targets, while building reusable platforms that make those insights scalable across therapeutic modalities. For an experienced computational biologist, this is a rare chance to work on foundational target biology with a global biotech leader, applying long-read transcriptomics, single-cell atlases and transcriptional foundation models inside a genuinely cross-functional research environment with strong scientific visibility.
Therapy Business Manager – Gastroenterology (GI Optima)
Abbott
Bikaner0-2 Years · Onsite25 SeptAbbott's Established Pharmaceuticals Division (EPD) is hiring a Therapy Business Manager for its GI Optima gastroenterology portfolio in Bikaner, Rajasthan. This frontline commercial role sits exactly where Abbott's science meets patient care — you own a defined territory and are accountable for converting brand strategy into real prescription behaviour among gastroenterologists, physicians, paediatricians and key opinion leaders. The GI segment is among Abbott EPD's most competitive, highest-growth therapy areas in India, making this position a genuine launchpad for a long-term pharmaceutical commercial career. You will operate with considerable autonomy, manage chemists and stockists, and act as the visible face of a globally respected, science-led organisation. For professionals who thrive on measurable targets, relationship-driven selling and credible clinical conversations, this is a high-visibility opportunity backed by structured MNC training.
Territory Business Manager – Restora (Probiotics & Gut Health)
Abbott
Dhule0-2 Years · Onsite25 SeptAbbott's Established Pharmaceuticals Division (EPD) is a cornerstone of the company's emerging-market strategy, delivering trusted, affordable branded generics across cardiology, diabetes, pain management and women's health. The Territory Business Manager for Restora — Abbott's flagship gut-health and probiotic brand — owns the Dhule and surrounding North Maharashtra territory, translating brand strategy into prescriptions, pharmacy pull-through and sustainable market share growth. This is a frontline commercial role with genuine ownership: you design your own call plan, negotiate shelf presence with chemists and stockists, and build prescribing conviction among physicians. Because the territory runs with minimal day-to-day supervision, performance is transparent and meritocratic, and strong performers are fast-tracked into Area Business Manager and brand marketing roles. For a BSc or B.Pharm graduate seeking a high-visibility entry point into a multinational's commercial engine, it is an exceptional launchpad.
Ophthalmology Squad Lead
Roche
Kolkata5+ Years · Onsite25 SeptRoche’s Ophthalmology Squad Lead role in Kolkata is a senior commercial and strategic leadership position within one of the company’s most important therapy areas in India. The incumbent owns the Outcome Based Plan, translating disease-area strategy into measurable patient impact, partnerships and account penetration. This is a high-visibility opportunity to shape the ophthalmology ecosystem, lead cross-functional squads and co-create value propositions with key corporate and regional accounts. The position matters because Roche’s ophthalmology portfolio is central to future growth, requiring visionary leadership, execution excellence and uncompromising compliance. For an experienced pharma leader, it offers the chance to influence access, innovation adoption and team development while working with global and Indian stakeholders to improve retinal and eye-care outcomes.
Area Medical Advisor - Hepatology
Gsk
Kolkata0-2 Years · Onsite25 SeptGSK is seeking an Area Medical Advisor for Hepatology, a pivotal Medical Affairs role that bridges clinical science and commercial strategy across the Kolkata region. You will serve as the scientific anchor for hepatology brands, engaging Key External Experts and Key Opinion Leaders to ensure accurate, on-label medical communication. This position shapes medical education, scientific engagement, and brand strategy while supporting pharmacovigilance and field research feasibility. As GSK advances specialty medicines and vaccines in hepatology and infectious diseases, the Advisor ensures healthcare professionals receive evidence-based insights that improve patient outcomes. For an MBBS or MD professional with pharmaceutical experience, this role offers high visibility, cross-functional collaboration, and the chance to influence regional clinical practice. It is an exceptional opportunity to combine scientific expertise, stakeholder leadership, and patient impact within a global biopharma leader.
Electrical Engineering Technician – Pharmaceutical Manufacturing
Gsk
Nashik5+ Years · Onsite25 SeptGSK’s Nashik manufacturing site is a critical node in the company’s global supply chain, producing medicines and vaccines that reach patients worldwide. This Electrical Engineering Technician role is central to maintaining uninterrupted power and utility services across high-voltage and low-voltage systems, HVAC, boilers, chillers, and compressed air. By executing preventive, predictive, and breakdown maintenance, the technician directly protects product quality, regulatory compliance, and commercial output. The position offers a compelling career opportunity for hands-on electrical professionals who want to deepen their expertise in pharmaceutical manufacturing, automation, and GxP environments. Working cross-functionally with production, quality, and EHS teams, you will help GSK deliver on its ambition to impact 2.5 billion people by 2030 while building a resilient, future-ready engineering career.
Senior Statistical Programmer
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi's Business Operations hub in Hyderabad anchors a global network of centralized statistical, medical and commercial capabilities serving Specialty Care, Vaccines, General Medicines, Consumer Healthcare and R&D. Within that structure, the Senior Statistical Programmer is a linchpin of Medical Affairs biostatistics — converting raw clinical trial and registry data into rigorous, QC'd tables, figures and listings that underpin abstracts, posters, manuscripts and regulatory-grade evidence. The position sits at the intersection of statistical science and programming craft, giving the holder direct exposure to Sanofi's global portfolio and to senior biostatisticians across geographies. For experienced SAS programmers who want their code to shape how medicines are described to physicians, regulators and payers worldwide, this is a rare chance to combine deep technical work with visible scientific impact.
Associate Manager - Manufacturing Quality Assurance (Upstream)
Pfizer
Visakhapatnam5+ Years · Onsite25 SeptThis Associate Manager - MQA Upstream role at Pfizer’s Vizag sterile manufacturing site is a critical quality leadership position supporting cGMP compliance across solution/emulsion preparation, vial and ampoule washing, depyrogenation, filling, capping, and collection. The position safeguards patient safety and product quality for Pfizer’s sterile injectable portfolio, where regulatory scrutiny from USFDA, MHRA, and TGA is intense. By reviewing electronic batch records, assessing AMPS exceptions, overseeing alarm and trend reports, and investigating deviations, the MQA professional ensures every batch meets Pfizer standards and global regulatory expectations. This is a compelling opportunity for experienced QA professionals to deepen expertise in sterile manufacturing, electronic batch systems, and inspection readiness while influencing shop-floor quality culture, process simplification, and continuous improvement at one of Pfizer’s key India sites.
Associate Manager – Manufacturing Quality Assurance
Pfizer
Visakhapatnam5+ Years · Onsite25 SeptPfizer’s Associate Manager, Manufacturing Quality Assurance, based in Visakhapatnam, is a critical cGMP compliance role supporting terminal sterilization, visual inspection and packaging operations. The position ensures that manufacturing processes, batch records and equipment systems remain inspection-ready for global regulators such as USFDA, MHRA and TGA. This is not a generic QA job: it directly protects patient safety, product quality and Pfizer’s commercial supply continuity. The role offers a strong platform for experienced pharma QA professionals to deepen expertise in sterile operations, electronic batch record review, deviation/AMP impact assessment and audit management. With Pfizer’s science- and risk-based quality culture, the successful candidate gains exposure to advanced manufacturing systems, cross-functional troubleshooting and process simplification, making it an excellent long-term career move within global pharmaceutical operations.
Medical Advisor Head Office - Mumbai
Boehringer Ingelheim
Mumbai5+ Years · Onsite25 SeptMedical Affairs role focused on scientific engagement, therapeutic-area insights, medical projects, KOL development, medico-marketing strategy, product registration support and medical labeling activities.
Manager QA - EPD Quality Systems
Abbott
Mumbai5+ Years · Onsite25 SeptManager QA – EPD Quality Systems responsible for managing Quality Systems related initiatives within the EPD Quality System organization to ensure safe, effective and quality products.
Area Manager
Lupin
Ahmedabad5+ Years · Onsite25 SeptManage regional sales operations, drive primary and secondary sales targets, and lead a team of medical representatives in Ahmedabad.
Scientist, Biomarker Analysis
Amgen
Hyderabad5+ Years · Onsite25 SeptAmgen's Scientist, Biomarker Analysis role in Hyderabad is a strategic addition to the Global Development - Precision Medicine organization, specifically within Computational Biology and Translational Analytics. As Amgen expands its India innovation footprint, this position will deliver high-quality clinical biomarker analytics across oncology, inflammation, rare disease, cardiovascular/metabolic, and obesity programs. The scientist will transform complex multi-omics, imaging, and clinical trial data into actionable translational insights that inform target engagement, patient stratification, mechanism validation, and benefit-risk decisions. This is a compelling opportunity for a quantitative biologist to work at the interface of drug development, advanced statistics, and responsible AI, influencing global portfolio decisions while helping build a high-impact precision medicine capability at Amgen India. The role offers deep scientific ownership, cross-functional collaboration, and exposure to late-stage clinical programs.
Therapy Business Manager – Gastroenterology (GI Prima)
Abbott
Bathinda0-2 Years · Onsite25 SeptAbbott's Established Pharma Division (EPD) is a cornerstone of the company's India business, and the GI Prima portfolio sits at the heart of its gastroenterology franchise — a high-growth therapy area spanning proton-pump inhibitors, prokinetics, probiotics and digestive-health brands. The Therapy Business Manager (TBM) is the commercial face of this franchise across the Bathinda belt of Punjab, translating brand strategy into real prescriptions at the point of care. This is a genuinely entrepreneurial field role: you effectively own a territory's performance, build durable relationships with gastroenterologists, physicians, chemists and stockists, and see your impact reflected in weekly prescription audits. For ambitious pharma sales professionals, it offers structured MNC training, clear promotion pathways into Area Business Management, and the credibility of representing a globally respected healthcare brand.
Brand Manager - Adult Vaccines
Gsk
Mumbai2-5 Years · Onsite25 SeptGSK’s Adult Vaccines Brand Manager role in Mumbai is a strategic commercial position responsible for shaping how adult immunization brands are positioned, promoted, and grown across India. As vaccines become a cornerstone of GSK’s infectious disease portfolio, this role directly influences market share, HCP engagement, and patient access. The Brand Manager partners with sales, medical, regulatory, market access, and creative agencies to translate insights into differentiated campaigns. It is a compelling opportunity for pharma marketing professionals who want to combine scientific literacy with omnichannel execution, competitive intelligence, and P&L ownership. The position offers high visibility within a global biopharma leader and a chance to build expertise in one of the fastest-evolving preventive healthcare categories.
Associate Manager, Externally Sponsored Research
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi Business Operations (SBO) in Hyderabad seeks an Associate Manager, Externally Sponsored Research (ESR) to oversee investigator-sponsored studies and externally sponsored collaborations from concept submission through closeout. This role sits at the intersection of clinical research, medical governance, and operational excellence, ensuring that unsolicited research support requests are routed for scientific review and managed in compliance with Sanofi SOPs, ICH-GCP, and local regulations. It is critical to Sanofi's Specialty Care, Vaccines, General Medicines, and R&D pipelines because ESRs generate real-world evidence and expand research partnerships. The position offers deep exposure to global stakeholders, SRC coordination, study start-up, product supply, contracting, and audit readiness. For professionals with clinical trial project management experience, it is a compelling opportunity to build specialized expertise in externally sponsored research operations while contributing to compliant, timely delivery of studies that inform medical and commercial strategy.
R&D Global Regulatory Affairs CMC Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi’s Global Regulatory Affairs CMC & Device Organization seeks an R&D GRA CMC Lead in Hyderabad to shape regulatory strategies for pharmaceuticals, biologics, vaccines, and combination products. This senior role is central to Sanofi’s pipeline, bridging R&D, manufacturing, and health authorities such as the US FDA and EMA. The CMC Lead ensures dossiers meet global quality and compliance standards, accelerates approvals, and mitigates regulatory risks across the product lifecycle. As a strategic partner, the position influences cross-functional teams, regulatory policy, and digital innovation, including AI-enabled regulatory workflows. For experienced CMC professionals, this is a high-visibility opportunity to lead complex submissions, negotiate with regulators, and advance patient access to innovative therapies while growing within a world-class regulatory network.
Assistant Manager – Pharmacovigilance Local Case Intake (Japanese Language)
AstraZeneca
Bengaluru5+ Years · Onsite25 SeptAstraZeneca's Local Case Intake function is the front door of the company's patient-safety ecosystem, and this Assistant Manager role owns it for the Japanese market. Leading a team of Local Case Intake Advisors, you will make sure every adverse event report originating from Japanese Marketing Companies is captured, triaged, followed up and submitted within regulatory clocks. Because Japan is one of AstraZeneca's largest and most tightly regulated commercial markets, accuracy here directly protects licence continuity, Health Authority credibility and patient trust. This is a compelling next step for a pharmacovigilance professional with Japanese language capability who wants to move from individual case processing into people leadership, gaining structured exposure to PMDA interactions, Pharmacovigilance System Master File governance, inspection readiness and global safety transformation work inside a digitally enabled organisation.
Associate Manager - MSAT (Commissioning & Qualification)
Pfizer
Vizag5+ Years · Onsite25 SeptPfizer’s Manufacturing Science & Technology (MSAT) group at Vizag plays a critical role in commissioning, qualification and validation of sterile injectable manufacturing assets. The Associate Manager – MSAT (C&Q) ensures equipment, utilities, facilities and processes are qualified to cGMP, FDA and Pfizer Quality Standards, directly protecting product sterility, patient safety and regulatory compliance. This position matters because Vizag supports regulated-market injectables, where robust validation underpins every batch release. The role offers exposure to complex sterile processes, cleaning validation, computer system validation, audits and technology transfers. For pharma professionals with QA, validation or sterile manufacturing experience, it is a compelling opportunity to deepen technical expertise, work cross-functionally and influence compliance strategy at a global scale while building a pathway toward senior quality and MSAT leadership.
Regulatory Affairs CMC Team Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptThis R&D GRA CMC Team Lead role at Sanofi in Hyderabad is a senior regulatory affairs leadership position within the Global Regulatory Affairs CMC & Device Organization. The incumbent will shape global Chemistry, Manufacturing, and Controls strategies for pharmaceuticals, biologics, vaccines, and combination products, directly influencing approval timelines and lifecycle management. As a critical bridge between technical development, manufacturing, and health authorities, this role ensures Sanofi's innovative therapies reach patients with speed and compliance. The position offers exceptional exposure to FDA, EMA, and other global regulators, matrixed project teams, and cutting-edge digital regulatory tools such as Veeva Vault. For regulatory professionals seeking to lead strategy, mentor specialists, and drive organizational change in a world-class biopharma environment, this is a compelling career step with significant influence on Sanofi's commercial and clinical pipeline.
Medical Science Liaison
Bayer
Delhi NCRFreshers · Onsite24 SeptServe as a scientific and medical liaison with healthcare professionals, thought leaders, medical societies, and other external stakeholders. The role focuses on scientific information exchange, medical education, advisory-board support, congress engagement, clinical-trial knowledge, and therapeutic-area insights.
Kit Production Assistant III
Labcorp
Bangalore2-5 Years · Onsite24 SeptSupport clinical research kit inventory operations by maintaining project and site-level Kit Material Supply systems, processing work orders, resolving kit-supply issues, supporting investigator sites, and ensuring accurate documentation and timely service delivery.