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 1–24 of 24 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.
Manager - Legal
Motherhood Hospitals
Bangalore5+ Years · Onsite1 OctLead all aspects of corporate legal operations, contract drafting, litigation management, and stakeholder advisory.
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.
Nursing In-Charge - Emergency
Manipal Hospitals
Bangalore5+ Years · Onsite26 SeptNursing In-Charge for the Emergency Department responsible for overseeing daily operations, managing nursing staff, and ensuring compliance with clinical protocols.
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.
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 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.
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.
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.
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.
Implementation Consultant and Integration Developer
Infosys Limited
Bangalore5+ Years · Onsite18 SeptDrive end-to-end integration architecture and technical implementation for enterprise contact center (CCaaS) platforms and modern voice/API ecosystems.
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.
Senior Analyst, Advanced Analytics
Labcorp
Bangalore5+ Years · Onsite11 SeptSenior analytics role focused on advanced SQL, statistical analysis, experimentation, dashboards, automation and AI-assisted workflows to turn marketing and commercial data into actionable business decisions.
Senior Specialist / Expert - Safety Medical Writer
Merck KGaA
Bangalore5+ Years · Onsite11 SeptSupport Global Patient Safety teams by producing high-quality pharmacovigilance medical-writing deliverables, including periodic safety reports, signal assessments, benefit-risk documents, risk-management plans, patient safety narratives, and health hazard reports.