Jobs at Pfizer

Provides comprehensive administrative support to the Head of Oncology Portfolio Management and senior team members. Responsibilities include coordinating governance meetings, managing calendars, travel, expenses, confidential materials, office supplies, SharePoint permissions, onboarding, and complex administrative issues. The role requires independent judgment, strong organization, collaboration, communication, and advanced proficiency with Microsoft Office, SharePoint, Teams, Ariba, and related systems.

Provides technical expertise and operational support for sterile inspection of injectable pharmaceutical products. Troubleshoots automated inspection equipment, investigates complex deviations, performs root-cause analysis, develops and validates manufacturing processes, leads improvement projects, supports audits and compliance activities, trains operations colleagues, and serves as a site SME for automated visual and spectroscopy-based inspection technologies.

Leads specialty-care commercial analytics and insights for Pfizer brands, using secondary data, AI-enabled tools, and advanced analytics to identify business drivers, risks, and opportunities. Partners with brand, data science, market access, and commercial teams to shape strategy, standardize methodologies, modernize reporting, and communicate actionable recommendations to senior leaders. Oversees vendor analytics, ensures data quality, and provides therapeutic-area expertise across patient segments, market dynamics, and competitive trends.

Supports regulated in vivo research studies involving mouse and rat care, welfare, handling, injections, recordkeeping, and dataset analysis. Performs approved non-surgical procedures, applies the 3Rs, maintains laboratory standards, and may conduct ELISAs, blood sampling, reagent ordering, and data analysis. The role requires a BSc or equivalent experience, a Home Office Personal License, regulated animal-handling experience, and strong organizational and communication skills.

Leads moderately complex pharmaceutical and technical transfer projects, managing schedules, budgets, milestones, risks, issues, dependencies, resources, and cross-functional accountability. Oversees improvement initiatives, prepares status reports, resolves project issues, and supports operational teams in a regulated cGMP manufacturing environment. The role requires independent judgment, stakeholder communication, project coordination, and occasional support for global calls or 24/7 manufacturing operations.

Leads environmental health and safety strategy and compliance for Pfizer’s Bothell campuses. Oversees EHS management systems, regulatory permits, audits, inspections, risk reduction, emergency preparedness, contractor management, budgets, and environmental initiatives. Partners with site leadership, research teams, regulators, and regional peers to drive continuous improvement. Manages and develops EHS personnel while supporting biosafety, laboratory safety, fire and life safety, occupational hygiene, and capital projects.

Leads field medical strategy and stakeholder engagement for Pfizer vaccines and antivirals across an assigned territory. Provides scientifically accurate medical education, communicates clinical and outcomes data, supports clinical trials and investigator-sponsored research, leads advisory boards, develops medical account plans, and shares stakeholder insights. Collaborates with Medical Affairs, HEOR, research, and cross-functional teams while mentoring colleagues and ensuring compliant, patient-focused communications. Requires 40–50% travel and strong expertise in vaccines or antivirals.

Develops global medical communications content, including manuscripts, abstracts, congress materials, literature reviews, educational resources, presentations, and multimedia. The role researches, organizes, interprets, quality-checks, and ensures compliant delivery of medical content while coordinating with cross-functional teams. Responsibilities also include project tracking, issue resolution, stakeholder collaboration, and adoption of new content creation tools, including generative AI platforms.

Drives sales and develops customer relationships across an assigned neuroscience territory. Engages healthcare providers in person and virtually, creates territory call plans, uses analytics to identify opportunities, educates customers on approved products and disease-state information, collaborates cross-functionally, and completes administrative responsibilities compliantly.

Provides nursing care to healthy participants in first-in-human and early-phase clinical trials. Responsibilities include monitoring participants, taking vital signs and ECGs, collecting blood samples, administering medications, ensuring safety and protocol compliance, maintaining data accuracy, and collaborating with multidisciplinary research teams. The role includes structured training in clinical research and requires flexible shift work, including alternating weekends and occasional voluntary nights.

The Vaccines Field Medical Director provides therapeutic-area and product expertise to external medical stakeholders across an assigned territory. Responsibilities include developing medical engagement strategies, delivering scientific education, supporting clinical trials and investigator-sponsored research, leading advisory boards, sharing stakeholder insights, collaborating with Medical Affairs and cross-functional teams, supporting patient advocacy efforts, and mentoring colleagues. The role requires an MD or DO, extensive stakeholder communication, compliance with medical policies, leadership capabilities, and 40–50% travel.

Manages Quality Management and Commercial Quality services from Pfizer’s Istanbul service center. Oversees quality events, investigations, CAPA, audit remediation, reporting, analytics, governance, service transitions, and stakeholder engagement. Drives process standardization, automation, AI-enabled solutions, continuous improvement, data stewardship, and scalable service delivery while ensuring compliance with quality standards and timelines.

A 3–6 month internship at Pfizer Newbridge for currently enrolled Science, Engineering, or related STEM students. Interns gain hands-on experience in pharmaceutical manufacturing, engineering, quality, supply chain, and business operations while contributing to projects and developing technical and professional skills. Applicants must be legally eligible to work in Ireland, remain enrolled during recruitment, and be available for at least three months in 2027.

Lead development and execution of public and private market access strategies in India. Map reimbursement pathways, secure formulary inclusion, build private-sector access partnerships, develop HEOR and value evidence, track policy changes, and engage stakeholders across government, payers, hospitals, and internal cross-functional teams to drive uptake of innovative therapies and adult vaccination.

Executes and oversees EMEA payroll and time-and-attendance processes, including payroll validation, reconciliations, statutory remittances, reporting, audits, complex adjustments, compliance, and employee inquiries. Collaborates with People Experience, Finance, and external vendors to maintain data integrity and service quality. Supports year-end filings, team training, system upgrades, process improvements, and payroll controls while handling confidential information.

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.

Designs and evaluates AI agents for site reliability and infrastructure operations. Responsibilities include creating agent workflows, prompts, retrieval and decision logic; building evaluation harnesses with ground-truth datasets and quality metrics; establishing reasoning guardrails; converting operational knowledge into retrievable context; and measuring improvements in toil and MTTR. The role partners with SRE, operations, platform, and AI teams to deploy reliable agent-assisted workflows.

Two-year Pfizer R&D rotational program for recent STEM graduates, featuring four six-month rotations across drug discovery, clinical development, regulatory operations, data analytics, computational biology, and laboratory research. Associates complete at least two laboratory rotations while developing technical expertise, business acumen, teamwork, and leadership skills through projects, mentorship, and cross-functional collaboration.

Leads regulatory execution hub teams managing multi-market pharmaceutical dossiers from initial applications through product withdrawal. Oversees regulatory document authoring, submission preparation, labeling and artwork updates, health-authority responses, dossier quality review, compliance, audit readiness, portfolio prioritization, operational efficiency, and cross-functional collaboration. Manages team performance, talent development, KPIs, quality metrics, and change initiatives while supporting global regulatory and commercial objectives.

Leads Pfizer’s oncology portfolio strategy, brand planning, campaign development, stakeholder engagement, forecasting, and promotional compliance. Adapts global strategies to local market needs, develops omnichannel demand-generation programs, coordinates cross-functional teams, manages revenue and A&P forecasts, and supports prelaunch planning and long-range portfolio growth.