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 176–200 of 287 jobs
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.
Regulatory Affairs Manager
AstraZeneca
Mumbai5+ Years · Hybrid25 SeptAstraZeneca is seeking a Regulatory Affairs Manager in Mumbai to lead complex regulatory strategies for its innovative biopharmaceutical portfolio. This senior role sits at the intersection of science, compliance and commercial delivery, shaping submissions, lifecycle management and health-authority interactions across global and regional markets. The position is critical to accelerating patient access to medicines, ensuring filings are right first time and maintaining AstraZeneca’s reputation with regulators. You will advise cross-functional teams, mitigate regulatory risks and champion process improvements in a company known for scientific leadership. For an experienced regulatory professional, this is a high-visibility opportunity to influence pipeline decisions, mentor talent and work with global stakeholders. It offers a rare blend of strategic ownership, operational depth and career-defining exposure within one of the world’s leading patient-focused pharmaceutical companies.
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.
Market Access Specialist
Roche
Delhi NCR5+ Years · Hybrid25 SeptRoche is seeking a Market Access Specialist to join its Access & Policy team in New Delhi, with coverage across Delhi and Haryana. This senior role is central to Roche's mission of expanding equitable healthcare access in India across oncology, ophthalmology, rare diseases and neurology. The position shapes evidence-based, innovative programs that strengthen health systems, support state-level partnerships, and improve prevention, early detection, screening and quality of care for underserved populations. Working closely with State Access Partners, government bodies, public health organizations and internal cross-functional teams, the incumbent translates strategy into scalable, measurable impact. For professionals passionate about health policy, access and system transformation, this is a rare opportunity to influence public-private collaboration at scale while advancing a global leader's patient-access agenda in India.
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.
Clinical Study Manager II
ICON
Bangalore5+ Years · Hybrid24 SeptManage day-to-day clinical trial activities and lead planning, execution, monitoring, and issue resolution for complex clinical studies. The role supports sponsor-dedicated clinical development programmes while ensuring regulatory compliance, data integrity, quality, timelines, and efficient resource utilization.
Manager QA – EPD Quality Systems
Abbott
Mumbai5+ Years · Onsite24 SeptManage Quality Systems initiatives within Abbott's EPD Quality System organization, supporting Quality Management System processes with emphasis on Third-Party Manufacturer and Supplier Quality Management. The role drives continuous improvement, regulatory compliance, global initiatives, and quality-system governance.
Senior Medical Advisor
Pfizer
Mumbai5+ Years · Onsite24 SeptProvide scientific and medical expertise to support medical strategy, launch readiness, evidence generation, and external engagement for Specialty Care and Internal Medicine pipeline products while ensuring scientific integrity and regulatory compliance.
Associate Consultant Neuro Surgery
Fortis Healthcare
Bangalore5+ Years · Onsite24 SeptSeeking an Associate Consultant Neuro Surgery to deliver expert surgical care, manage neurological disorders, and contribute to clinical excellence at People Tree Hospital.
Consultant – Anesthesiologist
AIMS India
Faridabad5+ Years · Onsite24 SeptSeeking an experienced Consultant Anesthesiologist to provide expert anesthetic care, manage critical care units, and ensure patient safety during surgical procedures.
Director, Process Development- Drug Product
Amgen
Hyderabad5+ Years · Onsite24 SeptLead and build the Drug Product Technologies organization at Amgen Hyderabad, driving process development, digital transformation, and global biotech deliverables.
Medical Governance Lead
Novartis
India5+ Years · Onsite24 SeptMedical Governance Lead accountable for strengthening governance, compliance, SOP adherence, MLR oversight, audit readiness and Managed Access Program governance across Medical Affairs activities in India.
Head of Manufacturing and Supply Services Hyderabad Hub
Sanofi
Hyderabad5+ Years · Hybrid23 SeptLead and direct large-scale manufacturing and supply operations and teams (400+ personnel) at the Hyderabad Hub.
Attending Consultant Radiology
Fortis Escorts Heart Institute & Research Centre
Delhi NCR5+ Years · Onsite23 SeptProvide expert radiological diagnostic and consultative services at Fortis Escorts Heart Institute in Delhi.
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Speciality Care Advisor - Cardiology (field based in Mumbai)
Bristol Myers Squibb
Mumbai5+ Years · Onsite23 SeptDrive territory performance for Cardiology by identifying and mapping healthcare accounts, engaging healthcare professionals, supporting scientific activities and executing commercial strategies in line with BMS objectives and values.
Director, Process Development - Drug Product
Amgen
Hyderabad5+ Years · Onsite23 SeptLead the establishment and growth of Amgen's Drug Product Technologies organization in Hyderabad, building a high-performing team and operating model while expanding global drug product process-development capabilities through technical, digital and cross-functional innovation.
Uro OT Incharge
Max Super Speciality Hospital
Delhi NCR5+ Years · Onsite22 SeptLead Uro OT nursing operations at Max Super Speciality Hospital, Noida 128, ensuring top-tier surgical safety, patient care, and team management.
Associate Manager SRC Governance
Sanofi
Hyderabad5+ Years · Hybrid22 SeptOur Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Main responsibilities: Committee review Governance team support to set up governance to review meetings for all 4 committee reviews for ESRs, Phase 1 studies, Global Health Studies and MRPTC as per the established operating model. Study Review Committee (SRC) Primary responsibility is to Set up governance to review approval meetings for all 4 committee reviews - Company Sponsored Studies & Externally Sponsored Collaborations (CSS & ESC), ISS, Global Health Studies as per the established operating model. Identify stakeholders, organize pre-SRC meetings, maintain Action Registers, and manage audit readiness. Medico-Regulatory Pharmacovigilance Transversal Committee (MRPTC) Lead the conduct of the MRPTC including preparatory meetings, minutes, follow-up, and stakeholder coordination. Phase I SRC Set up governance for Phase 1 study review approval meetings, ensure cross-functional alignment, and manage risks and timelines.
Medical Affairs Manager
Johnson & Johnson
Mumbai5+ Years · Hybrid22 SeptMedical Affairs leadership role supporting DePuy Synthes country strategy, evidence generation, stakeholder engagement, innovation and medical/scientific activities.
Regional Manager - Coronary & Renal Denervation
Medtronic
Hyderabad5+ Years · Remote22 SeptLead and coach a regional sales team to drive commercial growth and market adoption of advanced coronary and cardiovascular medical technologies at Medtronic.
Manager Regulatory Affairs
Abbott
Mumbai5+ Years · Onsite22 SeptExperienced Regulatory Affairs professional responsible for product registration submissions, regulatory strategy, agency interactions, lifecycle management, and regulatory support for established pharmaceutical products.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite22 SeptDirector-level clinical operations leadership role responsible for clinical trial delivery across India, from feasibility through site close. The position leads India-based teams and FSP partners while coordinating with global functional leaders, sites, investigators, vendors, and regulatory authorities.
Senior Manager, Analytics Products and Technology - Obesity
Amgen
Hyderabad5+ Years · Onsite21 SeptOwn the development and evolution of business-facing analytics and decision-support products for Amgen's global obesity business.
Regulatory Labeling Mgr
Amgen
Hyderabad5+ Years · Onsite21 SeptSupport the planning, coordination, and execution of EU and global labelling compliance activities within the Regulatory Affairs organisation.
Linux Platform Engineer
Eli Lilly and Company
Bangalore5+ Years · Onsite21 SeptLead the design, implementation, and management of enterprise Linux platforms and Ansible automation across hybrid multi-cloud environments.