Jobs at Pfizer

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.

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.

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 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.

Lead clinical development and regulatory strategy for assigned project in Japan, coordinating with global and local teams, KOLs, and stakeholders. Oversee study design, protocol documents, safety reviews, committees (IDMC/AC), and J-NDA submission materials while driving team leadership, stakeholder engagement, and process improvements.

Leads Pfizer Japan’s GU cancer Medical Affairs team, developing and executing medical strategies, engaging healthcare professionals and key opinion leaders, overseeing evidence generation, ensuring regulatory and safety compliance, managing budgets, and coaching Medical Affairs Scientists. The role coordinates cross-functional and global stakeholders, supports scientific communications, gathers customer insights, and contributes to business development and responses to critical supply issues.

Develops protein subunit vaccine production processes within Pfizer’s Early Bioprocess Development group. Responsibilities include optimizing cell line workflows, executing fermentation and bioreactor studies, analyzing process and molecular data, documenting experiments, preparing technical reports, and presenting findings to cross-functional teams. The role requires hands-on expertise in cell culture, molecular biology, flow cytometry, and process optimization while adhering to scientific, ethical, and regulatory standards.

Develop and execute access strategies for oncology assets, ensuring optimal patient access and alignment with stakeholder needs while managing pricing and reimbursement activities.

Owns the design and production delivery of an AI-driven SRE platform and agentic incident pipeline. Coordinates a Greece-based AI Operations pod, establishes safe agent capabilities and integration standards, and develops connectors, runbooks, observability, and guarded remediation workflows. The role applies AI, automation, SRE practices, and infrastructure expertise across hosting domains while ensuring reliability, auditability, rollback, measurable accuracy, and continuous toil reduction.

Build and maintain AI operations automation platforms, connectors, integrations, remediation playbooks, data pipelines, and evaluation tooling. Automate infrastructure administration using Ansible, Terraform, Python, PowerShell, and Bash. Improve hosting reliability through predictive operations, guarded remediation, rollback, auditing, testing, CI/CD, documentation, and continuous improvement. The role is hybrid in Greece and requires periodic international and domestic travel of less than 10%.

Leads hospital-focused pharmaceutical sales for sterile injectables by developing territory and account plans, engaging healthcare providers and key opinion leaders, promoting approved products, explaining access and reimbursement resources, and driving product demand. Builds customer relationships through virtual and in-person interactions, uses digital engagement tools and analytics, collaborates with medical and account teams, and provides compliant product and disease-state education.

Leads Pfizer’s U.S. Oncology Medical Affairs organization, including headquarters and field medical teams. Develops regional medical strategies, supports clinical development and asset lifecycle planning, oversees data generation and dissemination, builds KOL relationships, aligns medical and commercial priorities, manages budgets, and coaches a large, matrixed organization. Requires deep oncology expertise, pharmaceutical industry experience, clinical trial knowledge, and exceptional leadership.

Conduct drug discovery research in cardiovascular biology, focusing on identifying and validating therapeutic targets and biomarkers related to atherosclerosis. Design and execute cellular, molecular, imaging, ex vivo, and animal studies; analyze data; collaborate with internal and academic scientists; communicate findings through publications and presentations; uphold scientific and regulatory standards; and mentor junior scientists.

Leads regional activation of oncology patient advocacy partnerships and educational programs. Delivers or coordinates disease-state education, connects patients and caregivers with appropriate resources, manages sponsorships, budgets, events, and project plans, and reports insights and measurable outcomes. Collaborates across Pfizer teams, ensures compliance with CP208 and applicable regulations, strengthens advocacy relationships, and develops solutions supporting patient engagement and unmet patient needs. This field-based role requires substantial travel, occasional evening and weekend work, and operation of a company vehicle.

Investigates pharmaceutical manufacturing and laboratory quality issues, including deviations, out-of-specification results, and atypical investigations. Identifies root causes, recommends corrective and preventive actions, and ensures reports meet regulatory and company requirements. The role manages moderately complex projects, plans work activities, resolves problems, mentors colleagues, and collaborates across teams while following established procedures.