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 1–25 of 28 jobs
Principal Tech Engineer – Site Serialisation Systems
Gsk
Bengaluru5+ Years · Onsite6 days agoGSK is recruiting a Principal Tech Engineer to lead technical work on site serialisation systems within its PIMMS Manufacturing Track & Trace product. The position is hands-on, spanning solution design, validation, implementation and the resolution of complex integration failures across multiple manufacturing sites.
Director - SN Risk & Compliance Manager
Gsk
Bengaluru5+ Years · Onsite10 days agoGSK is hiring a Director - SN Risk & Compliance Manager in Bengaluru to hold the risk and compliance position of the ServiceNow and enterprise tools platform across its operational life. The role runs risk and compliance assessments on platform change, verifies control attestation before release, and maintains qualification and release evidence.
Quality Specialist (QMS, Documentation)
Merck
Bangalore5+ Years · Onsite4 OctQuality Assurance Specialist responsible for maintaining the Quality Management System, leading quality activities, ensuring regulatory compliance, and strengthening product and process quality within Merck's Life Science division in India.
Expert - Regulatory Labelling Operations
Merck KGaA
Bangalore5+ Years · Onsite3 OctThe Expert - Regulatory Labelling Operations role focuses on global labeling operational excellence, process optimization, compliance tracking and continuous improvement within Regulatory Quality Safety (RQS).
Assistant Manager, Clinical Data Management
Teva Pharmaceuticals
Bangalore5+ Years · Onsite2 OctLeads and supports Clinical Data Management delivery with subject matter expertise, study oversight, quality control and process improvement. The role combines technical CDM expertise with resource coordination, mentoring, standards development and audit support.
Medical Writing Specialist
Novo Nordisk
Bangalore5+ Years · Onsite1 OctSenior medical writing specialist role responsible for leading clinical reporting deliverables, setting direction for complex medical writing work, coordinating global stakeholders, and driving quality and process improvements across clinical development programmes.
GPV Professional, Case Processing
Teva Pharmaceuticals
Bangalore0-2 Years · Onsite30 SeptSupport global pharmacovigilance case processing by accurately processing adverse events, maintaining high-quality safety data, performing medical coding and data verification, managing follow-ups, and meeting regulatory and operational timelines.
Manager, Clinical Operations
Parexel
Bangalore5+ Years · Onsite29 SeptManager, Clinical Operations responsible for team oversight, clinical project delivery, resource planning, staff development, quality control, client management, and compliance with clinical research standards and regulations.
Quality Specialist (QMS, Documentation)
Merck KGaA
Bangalore5+ Years · Onsite29 SeptQuality Assurance Specialist responsible for managing QMS, quality documentation, audits, investigations, compliance, and continuous improvement within Merck's Life Science division in India.
Safety Operations Advisor 1
Novo Nordisk
Bangalore5+ Years · Onsite28 SeptProvide medical expertise across global pharmacovigilance operations by evaluating adverse events, performing medical reviews and causality assessments, ensuring regulatory reporting compliance, and driving consistent safety practices across clinical and post-marketing programs.
Zonal Business Manager - South - Lung Cancer
Johnson & Johnson
Bangalore5+ Years · Onsite28 SeptDrive business growth in the assigned South territory for the Oncology franchise, maintaining effective customer relations and maximizing sales objectives.
Therapy Business Manager – Gastroenterology (GI Prospera)
Abbott
Bengaluru0-2 Years · Onsite26 SeptAbbott's Established Pharmaceuticals Division (EPD) is a cornerstone of the company's emerging-market growth engine, and the GI Prospera franchise sits at the centre of its gastroenterology portfolio. As Therapy Business Manager, you own a defined territory — the requisition references Gorakhpur in the title while the requisition location is Abbott's Bangalore (Thungs Tower) office — and act as the commercial face of the division to gastroenterologists, consulting physicians, chemists and stockists. This is a high-autonomy, high-visibility field role: prescription generation, market-share expansion and relationship depth with key stakeholders directly shape divisional revenue. For professionals who want an MNC-caliber commercial career, Abbott offers structured selling systems, therapy-focused training and a clear pathway into senior sales and brand leadership across its India and global EPD network.
Assistant Manager, Clinical Data Management
Teva Pharmaceuticals
Bangalore5+ Years · Onsite26 SeptAssistant Manager responsible for leading and supporting Clinical Data Management activities, ensuring accurate and timely study delivery, quality compliance, process improvement and effective stakeholder coordination.
Senior Medical Writer
Gsk
Bengaluru2-5 Years · Onsite26 SeptGSK is a global biopharmaceutical leader focused on vaccines and specialty medicines across respiratory, immunology, oncology, HIV and infectious diseases. The Senior Medical Writer in Bengaluru sits within a high-impact R&D documentation function that translates complex clinical and regulatory data into clear, compliant submissions. This role directly supports protocols, clinical study reports, CTD modules, investigator brochures and health-authority responses, making it central to accelerating GSK's pipeline and patient access. Working in a global matrix with clinical leads, biostatisticians and asset teams, the writer ensures scientific integrity and timely delivery. For experienced medical writers, this is a compelling opportunity to deepen regulatory writing expertise, collaborate across therapeutic areas, and contribute to medicines and vaccines that impact billions. GSK's culture of ambition for patients, accountability and inclusion further makes this a strong career platform in India's fast-growing biopharma sector.
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.
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.
Analyst - Dangerous Goods
Merck KGaA
Bangalore0-2 Years · Onsite24 SeptSupport the safe, compliant, and efficient movement of goods across global supply chains while applying scientific and regulatory expertise to Dangerous Goods activities. The role combines compliance, cross-functional collaboration, process improvement, and global project support.
Senior Specialist Submission Management
Merck
Bangalore5+ Years · Onsite19 SeptSenior regulatory submission management role focused on planning, publishing, quality checking and dispatching regulatory submissions to Health Authorities.
Manager, RA Publishing & Submissions
Astellas
Bangalore2-5 Years · Onsite19 SeptManager-level Regulatory Affairs Publishing & Submissions role focused on global regulatory submissions, publishing operations, submission standards, quality control and regulatory operations.
Safety Surveillance Adviser I
Novo Nordisk Global Business Services (GBS)
Bangalore2-5 Years · Onsite19 SeptSafety Surveillance Adviser I supporting Global Patient Safety activities across the lifecycle of Novo Nordisk medicines, including safety surveillance, signal and aggregate management, safety labelling, regulatory safety reporting, and cross-functional safety communication.
Quality Specialist (QMS, Documentation)
Merck
Bangalore5+ Years · Onsite18 SeptQuality Assurance Specialist responsible for QMS management, audits, investigations, quality documentation, regulatory compliance, staff training, quality metrics, and continuous improvement within Merck's Life Science division in India.
Safety Surveillance Adviser I
Novo Nordisk
Bangalore2-5 Years · Onsite16 SeptSafety Surveillance Adviser role within Global Patient Safety, supporting product safety surveillance, safety labelling, aggregate reporting, risk management and proactive safety communication across the medicine lifecycle.
Communication BP, LS India & Communications Lead, India
Merck
Bangalore5+ Years · Onsite16 SeptLead the end-to-end communications agenda for Merck's Life Science business in India, shaping brand presence, employee engagement and external communications while translating regional and global strategy into locally relevant narratives.
Senior Specialist Submission Management
Merck Group
Bangalore5+ Years · Onsite13 SeptSenior regulatory submission management specialist responsible for planning, compiling, publishing, quality-checking, and dispatching regulatory submissions while ensuring compliance, data integrity, and submission timelines.
Sr. International RA Specialist
BD
Bangalore5+ Years · Onsite13 SeptSenior Regulatory Affairs professional responsible for supporting global medical device registrations and lifecycle activities across multiple international markets. The role combines regulatory strategy, technical documentation review, risk assessment, and cross-functional coordination to enable compliant market access.