Jobs at Pfizer

Support local pharmacovigilance safety data management by maintaining legally required documentation, supporting report submission and distribution, tracking follow-up letters, assisting inspection preparedness, and applying company SOPs for case receipt and archiving. Work under supervision and use relational databases and office IT tools.

Lead administration and continuous improvement of Veeva eQMS for Regulatory Quality Assurance. Own access management, release coordination, reporting, and user documentation. Provide Vault configuration expertise, triage enhancement requests, represent Digital Systems in cross-functional programs, support data extracts and reporting, and drive AI-enabled process improvements and platform transformation within a GxP-regulated pharmaceutical environment.

Support engineering and manufacturing by preparing documentation, analyzing data, running tests, troubleshooting equipment, leading meetings, managing change controls and requalification packages, ensuring GxP compliance, and developing SOPs and technical standards to support site operations and regulatory audits.

The MQG Senior Associate supports medical quality oversight, manages inspection readiness, and handles quality events at Pfizer.

The Cloud Engineer will enhance cloud infrastructure, develop automation workflows, ensure security compliance, and collaborate on cloud solutions. Ideal candidates have cloud engineering experience and proficiency in Infrastructure as Code.

Perform microbiology QC testing (water analysis, sterility, endotoxin, MLT, CCIT), prepare media and cultures, sample and label materials, verify equipment, analyze and record data in computerized systems, maintain GMP/GLP documentation, revise SOPs, and support projects under supervisor direction.

Manage supply assurance and inventory for a pharmaceutical product portfolio: set inventory targets, monitor shelf-life, plan product launches and changes, perform root-cause analysis of deviations, drive improvement plans, support audits, and liaise with brand and manufacturing stakeholders.

Perform clinical data review and query management, support database design, testing, validation and implementation of EDC and other collection tools, maintain CDS documentation in the TMF, support data cleaning, visualization, DM metrics and database release to ensure data integrity and regulatory readiness.

Designs, develops, and maintains high-quality clinical databases; creates data capture solutions with study teams; ensures data integrity and standards compliance; learns and applies Pfizer database technologies; follows SOPs.

Perform, optimize, and troubleshoot NGS and single-cell genomics workflows including sample/tissue processing, nucleic acid extraction, library prep, sequencing, QC, and upstream data quality assessment. Validate and implement new assays and platforms, document SOPs and ELN records, train staff, and support cross-disciplinary research to deliver high-quality genomic datasets for drug discovery and preclinical development.

Lead data management, reporting, and analytics for clinical/medical evidence activities. Manage complex projects, allocate resources, develop solutions, ensure regulatory-compliant data standards, partner with business leadership, and build diverse talent pipelines to deliver timely, high-quality clinical data to stakeholders.

Perform GMP analytical testing of raw materials using HPLC, GC, FTIR/IR, UV, pH, titrations and wet chemical methods. Record and maintain cGMP-compliant data, identify and help investigate OOS results or instrument issues, support continuous improvement and lab visual management, and collaborate with the QC raw materials team.

Lead country-level regulatory strategy and execution for licensed and development products. Provide regulatory advice to cross-functional teams, manage national submissions, NRAs interactions, variations, renewals, device support, supply continuity, and regulatory databases while ensuring compliance, inspection readiness, and stakeholder engagement.

Lead development and execution of market access, pricing, and reimbursement strategies for pipeline and in-line assets. Integrate health economic evidence and payer insights, lead pricing projects and submissions, collaborate cross-functionally, manage budgets and timelines, engage external stakeholders (payers, HTA bodies, patient groups), and drive capability building and continuous improvement across the team.

Provide regulatory support for international country/cluster teams across product lifecycle including initial registrations, lifecycle management, and withdrawals. Author and review M1 local dossier components, coordinate HA query responses, support tenders, audits, labelling and launch planning, and ensure timely, compliant dossier submissions. Partner with Submission/Dossier Managers, identify regulatory requirements and emerging risks, and implement process efficiencies to meet quality and timeline goals.

Senior sales role replacing an existing team member. Base moved to Mumbai; responsible for covering West region (Mumbai, Pune, Ahmedabad). On-premise position at Pfizer focused on regional sales coverage and territory management.

Promote cardiovascular therapies within an assigned territory by driving sales, building in-person and virtual relationships with providers, executing territory call plans, leveraging analytics and digital tools, educating on product and disease state, collaborating cross-functionally, and completing compliant administrative tasks.

The Senior Manager, Field Medical, MD is responsible for executing medical strategies and engaging healthcare professionals. This role includes scientific communication, patient-focused discussions, and collaborating with internal teams to optimize care delivery and support clinical trials.

The Senior Manager, Field Medical oversees medical strategy and supports scientific exchange, collaborating with healthcare professionals to address clinical practice gaps and enhance patient outcomes.

Oversee engineering project operations, manage budgets and schedules, facilitate team communication, conduct risk analysis, and mentor team members in a pharmaceutical context.