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 26–50 of 115 jobs
Filling Instrumentation Engineer
Pfizer
Visakhapatnam2-5 Years · Onsite4 OctPfizer's Vizag facility is a cornerstone of its global sterile injectables and vaccine manufacturing network. The Filling Instrumentation Engineer role is central to maintaining uninterrupted, compliant operation of critical fill-finish equipment, including vial washing, tunnel sterilization, filling, capping, and inspection lines. By ensuring precise calibration, predictive maintenance, and rapid troubleshooting of instrumentation and automation systems, this engineer directly supports the delivery of life-saving medicines to patients worldwide. The position offers a unique opportunity to work with advanced Siemens, Allen-Bradley, or DeltaV platforms in a GMP-regulated environment. As part of a forward-thinking engineering team, you will contribute to capacity expansions, automation upgrades, and continuous improvement projects, accelerating your career in pharmaceutical engineering while making a tangible impact on global health.
Medical Writer
Thermo Fisher Scientific
Remote2-5 Years · Remote3 OctMedical Writer responsible for producing high-quality clinical and scientific documents for pharmaceutical and CRO clients, supporting projects from planning through final delivery in a fully remote India role.
Officer / Senior Officer – Quality Assurance (OSD)
Sun Pharmaceutical Industries Ltd
Halol2-5 Years · Onsite2 OctQuality Assurance opportunity at Sun Pharma's Halol plant focused on in-process quality assurance, batch documentation, validation, manufacturing oversight and cGMP compliance for oral solid dosage (OSD) operations.
Medical Writer II (MLR Reviewer)
Syneos Health
Delhi NCR2-5 Years · Hybrid2 OctMedical Writer II responsible for scientific writing, publication deliverables and medical-legal-regulatory review readiness. The role combines end-to-end medical writing, Veeva document management, MLR review, publication planning and cross-functional collaboration.
Clinical Data Programmer II
Novotech
India2-5 Years · Hybrid2 OctDrive core clinical trial programming, database design, and data validation activities at a leading global CRO, ensuring strict compliance with GCDMP and ICH-GCP standards.
Scientific Writer - Health Economics and Value Assessment (HEVA)
Sanofi
Hyderabad2-5 Years · Onsite1 OctSanofi’s Global Hub in Hyderabad is a strategic engine for medical, HEVA, and commercial excellence. As a Scientific Writer – Health Economics and Value Assessment (HEVA), you will translate complex health economic and value evidence into clear, compliant publications and communication tools. This role is pivotal for demonstrating product value to payers, healthcare professionals, and internal stakeholders, directly supporting access and reimbursement decisions across Specialty Care, Vaccines, General Medicines, and CHC. You will partner with global HEVA, RWE, and scientific communication teams, managing deliverables from manuscripts and abstracts to Core Value Decks. This is an outstanding opportunity to build therapeutic area expertise, influence global value narratives, and grow within a world-class pharmaceutical organization committed to innovation and patient impact.
Mgr, Regulatory Consulting (Office based)
Syneos Health
Hyderabad2-5 Years · Hybrid1 OctManager, Regulatory Consulting leads regulatory consulting projects, regulatory submissions, client engagements, project teams, and people-management activities while providing strategic and operational regulatory advice across pharmaceutical and related product development programs.
Scientific Writer HEVA
Sanofi
Hyderabad2-5 Years · Onsite1 OctScientific Writer – Health Economics and Value Assessment (HEVA) develops high-quality HEVA communications and evidence-based content supporting product value, access, and reimbursement decisions across global business units.
Senior Officer / Executive - Direct Procurement
Sun Pharmaceutical Industries Ltd
Mumbai2-5 Years · Onsite1 OctManage direct procurement of packaging materials for commercial sites and R&D locations, ensuring timely purchase orders, vendor coordination, delivery tracking, quality documentation, and procurement reporting.
Manager / Senior Manager - Medical Science Liaison
Eli Lilly and Company
Delhi NCR2-5 Years · Onsite1 OctField-based Medical Science Liaison role focused on Cardio-metabolic diseases, scientific exchange with healthcare experts, medical insights, strategic territory planning, and cross-functional collaboration.
Central Monitor Senior Associate
Amgen
Hyderabad2-5 Years · Onsite1 OctCentral Monitor Senior Associate independently performs proactive, data-driven central monitoring across clinical studies, using analytics and structured review to detect risks affecting patient safety, data quality, and protocol adherence.
Associate Project Specialist - Medical Communications
Sanofi
Hyderabad2-5 Years · Onsite30 SeptThis Associate Project Specialist – Medical Communications role at Sanofi in Hyderabad sits within Sanofi Business Operations (SBO), a centralized hub supporting Specialty Care, Vaccines, General Medicines, Consumer Healthcare, and R&D. The position is pivotal to delivering high-quality scientific publications and medical education materials—slide decks, abstracts, posters, and manuscripts—that communicate Sanofi’s clinical evidence to healthcare professionals, regulators, and payers. By coordinating project timelines, compliance submissions, budgets, and stakeholder communication, the specialist ensures scientific writers can focus on content excellence. This is an exceptional opportunity for life-sciences graduates to gain end-to-end exposure to medical publications, publication management tools like iEnvision and PromoMats, and global medical affairs operations. It offers a launchpad into medical writing, publications management, or scientific communications leadership within a top-tier pharmaceutical company.
Engagement Analyst – External Expert Engagement Services
AstraZeneca
Bengaluru2-5 Years · Hybrid30 SeptThe Engagement Analyst role within AstraZeneca's External Expert Engagement Services (E3S) sits at the intersection of Medical Affairs, Commercial and Compliance operations. Based at Manyata Tech Park, Bangalore, this individual-contributor position governs the end-to-end lifecycle of engagements with healthcare providers and patients — advisory boards, consulting assignments and speaking programmes that shape how AstraZeneca's medicines are understood, prescribed and adopted. Because every such engagement carries transparency and anti-bribery obligations, the analyst protects AstraZeneca's licence to operate while accelerating scientific exchange. For professionals with 1–5 years of experience in regulated contracting or compliance workflows, the role offers global exposure, direct partnership with Medical Affairs, Nominated Signatories and Legal, and a clear pathway into compliance, medical affairs operations or risk management careers.
Pharmacovigilance Reporting Associate
ICON
Bangalore2-5 Years · Remote30 SeptSupports accurate and timely preparation, review and submission of pharmacovigilance safety reports for clinical trials and post-marketing activities. The role combines safety-report preparation, adverse-event data analysis, regulatory compliance and cross-functional collaboration.
Senior Global Regulatory Scientist
ICON
Bangalore2-5 Years · Hybrid30 SeptSenior Global Regulatory Scientist responsible for leading global clinical-trial regulatory activities, submission strategy, regulatory project teams, client deliverables, and compliance across pharmaceutical clinical trials in India.
Associate Quality Complaints
Amgen
Hyderabad2-5 Years · Onsite30 SeptOwn and execute quality complaint activities across the global complaint process, ensuring compliant handling, accurate records, timely closure, and appropriate escalation. The role connects customer feedback with quality processes and continuous improvement.
Associate II Reg Strategy, GRS Oncology
Pfizer
Chennai2-5 Years · Hybrid30 SeptSupport global regulatory strategy and lifecycle maintenance activities for oncology products, coordinating submissions, CMC Module 1 documentation, labeling, safety compliance activities, Health Authority responses, and cross-functional regulatory operations.
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Clinical Trial Support Specialist
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite30 SeptSupport end-to-end clinical trial submission operations by preparing submission-ready documents, maintaining clinical trial systems and data, coordinating regulatory milestones, and enabling efficient clinical development activities across the oncology portfolio.
Medical Writer I / Medical Writer II
Parexel
Bangalore2-5 Years · Hybrid30 SeptDevelop high-quality pharmacovigilance and regulatory safety documents, conduct signal detection and assessment, synthesize scientific evidence, and support regulatory compliance across the product lifecycle.
Specialist, Quality Services – Product Complaints
Sanofi
Hyderabad2-5 Years · Onsite29 SeptSanofi's Global Manufacturing & Supply Services hub in Hyderabad is the operational backbone of the company's worldwide product quality agenda, and this Specialist Quality Services (Product Complaints) position sits at the frontline of post-market surveillance. The role owns intake, triage, categorization and closure of Product Technical Complaints across medical devices, pharmaceuticals, biologics and combination products — a workflow that directly protects patient safety and feeds the investigation, field alert and pharmacovigilance machinery of a 110,000-person life-sciences leader. Because Sanofi is investing heavily in AI-driven data standards and reusable quality data, specialists here gain exposure to modern QMS tooling and global cross-functional stakeholders. For an early-career quality professional, it is an exceptional launchpad: high regulatory visibility, structured GxP discipline and a clear route into broader quality, compliance and pharmacovigilance careers.
Clinical Programmer I / II
AstraZeneca
Bengaluru2-5 Years · Hybrid29 SeptThe Clinical Programmer I/II role at AstraZeneca's Manyata Tech Park campus in Bangalore sits at the intersection of clinical science and software engineering — the precise place where modern drug development is being reinvented. Reporting into the Biometrics and Clinical Programming function, this individual-contributor position converts raw trial data from EDC and third-party vendors into validated datasets, automated quality checks and executive-ready dashboards that study teams use to spot anomalies weeks earlier. Because AstraZeneca's pipeline spans oncology, cardiovascular, respiratory and rare disease, the programmer's output directly shapes how quickly and confidently go/no-go decisions are made. For a technically strong SAS or Python developer who wants their code to carry patient-level consequence rather than purely commercial consequence, this is a rare hybrid of engineering craft, regulatory rigour and genuine therapeutic impact.
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Scientific Writer II
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite29 SeptScientific Writer II responsible for authoring and coordinating regulatory and clinical documents, integrating scientific, medical, and regulatory input while managing document strategy, review cycles, timelines, quality, and compliance.
Medical Science Liaison
Bayer
Delhi NCR2-5 Years · Hybrid29 SeptDrive scientific engagement and education as a Medical Science Liaison with Bayer in Delhi.
Clinical Monitoring (CM)
Syneos Health
Hyderabad2-5 Years · Hybrid29 SeptSupport clinical trial oversight through independent monitoring, patient-level data review, study and site-level trend analysis, risk identification, and risk-based quality management.
Senior Statistical Programmer
AstraZeneca
Bengaluru2-5 Years · Hybrid28 SeptBased at AstraZeneca's Manyata Tech Park campus in Bangalore, the Senior Statistical Programmer I role sits within the Oncology Biometrics Programming department—a critical function that turns raw clinical trial data into regulatory-ready evidence. As part of a global team dedicated to eliminating cancer as a cause of death, you will support and lead statistical programming activities across high-priority oncology studies, from clinical study report development to regulatory submissions and commercialisation. This is a compelling opportunity for an experienced SAS programmer who wants to see their code influence filings, accelerate patient access, and shape evidence-based decisions. AstraZeneca's deep pipeline, collaborative research culture, and investment in science and technology make this a career-defining platform for professionals who combine technical rigour with a passion for improving patient outcomes.