Pfizer

This role is for a Machine Operator at Pfizer's Puurs production facility in Belgium. The primary responsibilities include ensuring the optimal functioning of filling lines, preparing and starting production activities, setting up and adjusting machines, performing checks, resolving machine downtime and minor breakdowns, performing daily maintenance, and maintaining cleanliness and order. The role requires technical and process insight, the ability to work independently and as part of a team, and experience in a GMP environment. The company emphasizes quality, safety, innovation, and teamwork.

This role focuses on designing, implementing, and automating secure, scalable, and modern cloud platforms (AWS, Azure, GCP) using Infrastructure as Code (Terraform) and scripting (Python). It involves platform automation, security guardrails, compliance, and collaboration with other engineering teams to deliver cloud solutions within an enterprise environment.

Senior Cloud Engineer responsible for designing, building, and evolving secure, scalable, and highly automated cloud platforms across a multi-cloud environment. Focuses on cloud standards, reference architectures, and engineering best practices, with strong emphasis on Infrastructure as Code and automation.

This role is for a Development Head overseeing vaccine clinical research and development programs at Pfizer. The position requires extensive expertise in clinical research, program design, and regulatory activities to ensure successful implementation and registration of vaccine candidates. Responsibilities include leading global clinical research programs, providing scientific and procedural expertise, managing clinical project teams, and ensuring quality and safety across studies. The role also involves potential in-licensing reviews and contributing to business development. A medical degree and over 10 years of pharmaceutical industry experience in clinical research are required, with specific experience in end-to-end vaccine clinical development.

Senior Manager of Cyber Risk Management responsible for assessing, enhancing, and operationalizing the enterprise cyber risk program. This role involves setting strategy, developing policies, leading a team, and partnering with cross-functional teams to ensure technology, data, and business processes meet internal control expectations, security requirements, and global regulatory obligations. The role requires a strong understanding of various regulatory frameworks and industry standards.

Senior Manager, Data Protection for Pfizer's Global Cybersecurity Governance, Risk, and Compliance team. Responsible for establishing, governing, and operationalizing the enterprise data protection program globally, ensuring sensitive data is identified, classified, protected, and governed in alignment with regulations and policies. Partners with various teams to embed information protection requirements into technology and processes, drives control assurance, and reports on risk metrics.

The role is for a Manufacturing Technician at Pfizer in Zagreb, Croatia. The technician will participate in the production of active pharmaceutical ingredients and filled syringes, operate automated systems, maintain equipment, and ensure compliance with GMP and safety standards. The position involves shift work and requires a technical or scientific background.

Clinical Development Scientist, Director role at Pfizer focused on providing medical and scientific leadership for clinical trials in Inflammation and Immunology. Responsibilities include protocol development, study execution, data interpretation, risk management, and contributing to regulatory filings. Requires a PhD/PharmD with 5+ years of experience or MS with 7+ years, or BS/BA with 8+ years in a relevant science discipline, with deep knowledge of clinical development, ICH/GCP, and global regulatory requirements.

This role supports the Alliance Management and Business Operations Lead to manage a portfolio of research collaborations within Pfizer's Discovery Network. Responsibilities include coordinating alliance activities, managing contracts, facilitating governance meetings, and driving process improvements. The role requires knowledge of scientific operations, industry-academic alliances, and strong project management and communication skills.

Clinical Development Medical Executive Director in Hematology responsible for defining and executing the development strategy of hematology programs, leading clinical development subteams, and overseeing clinical trials.

Pfizer is seeking a Global Development Lead (MD, Sr. Director) for Internal Medicine to lead clinical development for assigned assets. This role involves designing, executing, and interpreting clinical studies, creating clinical development plans, and partnering with cross-functional teams and external stakeholders. The position requires extensive knowledge of clinical development, global regulations, and experience managing large teams in the biopharmaceutical industry.

Global Senior Medical Director responsible for the medical strategy of the Respiratory pipeline portfolio at Pfizer. This role involves external scientific engagement, supporting clinical studies, synthesizing insights, and shaping clinical development plans. It requires deep scientific expertise in pulmonology/allergy and a strong KOL network. The role collaborates across functions to define medical strategy, evidence generation plans, and stakeholder engagement, aiming to support the development and launch of innovative therapies.

Electrical Engineer focused on power distribution, automation systems, and vendor management for facility operations in a regulated R&D site. Responsibilities include engineering oversight, capital planning, and ensuring compliance for electrical and controls systems.

This role is for a Senior Associate Scientist in Pharmaceutical Research and Development at Pfizer, focusing on the formulation development and analytical characterization of biotherapeutics. The scientist will use various biophysical and biochemical techniques, support drug product manufacturing process development, and be responsible for data compilation and reporting. The position requires a Bachelor's or Master's degree in a relevant scientific field with 0-4 years of experience.

Senior Medical Director in Hematology responsible for supporting clinical trials, leading subteams in clinical development, and contributing to development strategies and regulatory interactions within the pharmaceutical industry.

This role focuses on the selection, qualification, and implementation of packaging components and container closure systems for pharmaceutical products, including combination products. It involves supporting formulation and process development, authoring technical documentation, participating in design control teams, conducting investigations, driving testing activities, and authoring regulatory submission content. The role requires strong technical expertise in parenteral packaging, medical device development, and regulatory compliance within a cGMP environment.

Seeking a Principal Scientist with expertise in enzymatic peptide synthesis and biocatalysis for innovative process development in peptide and API manufacturing. Requires a PhD and strong experimental skills, with industry experience preferred. Role involves designing, optimizing, and scaling enzymatic processes, collaborating cross-functionally, and contributing to scientific innovation.

Seeking a VP, Global Head of Statistics for Vaccine Clinical Research and Development (VCRD) to set vision and provide leadership for data management, modeling, and statistical advice across a complex portfolio of clinical development projects. This role requires deep expertise in statistical analysis tools, regulatory guidelines (FDA, ICH), and managing a large team of statisticians and modelers.

Associate's degree level role focused on operating, maintaining, and calibrating laboratory and robotic equipment in a regulated GxP setting for Pfizer's Vaccines division. Responsibilities include performing routine maintenance, documenting work in LIMS/ELN, and ensuring compliance with standard operating procedures.

Internship position for a pharmacy student at Pfizer in Berlin, Germany. The role involves supporting various medical and regulatory aspects of pharmaceutical development and product management, with opportunities to gain practical experience in areas like oncology, medical information, primary care, and regulatory sciences.

Internship opportunity at Pfizer in Freiburg, Germany, focusing on pharmaceutical production processes. The role involves learning about manufacturing, quality control, and development within a GMP-regulated environment. Interns will support daily operations, work on independent sub-projects, and gain insights into global pharmaceutical development.

This role is for a Principal Packaging Engineer in Biotherapeutics Pharmaceutical Research & Development at Pfizer. The individual will lead a team, provide strategic direction for laboratory operations supporting drug product and combination product development, and champion quality and compliance. Responsibilities include overseeing testing activities, component and container closure system selection, and authoring regulatory submission content. The role requires strong expertise in parenteral packaging, medical device/combination product development, and experience in GMP/ISO 13485 environments.

Pfizer is seeking a Pflichtpraktikant (m/f/d) in Finance to support Controlling, Reporting, and Month-End Closing. The role involves creating reports, analyses, and actively participating in daily business operations within a dynamic team. Candidates should be students in a business administration program with a focus on accounting, controlling, or finance, possess strong MS Office skills (especially Excel), have good numerical understanding, analytical skills, and be fluent in German and English.

Project Engineer Building at Pfizer in Belgium, responsible for the architectural and civil engineering aspects of capital projects, from feasibility studies to construction, validation, and startup. The role involves managing project plans, ensuring compliance with regulations and quality standards, and collaborating with internal and external stakeholders. Requires a Master's degree in Civil Engineering (Building) and strong project management skills.

The Maintenance Operator role at Pfizer in Zagreb, Croatia, focuses on the planned and corrective maintenance of equipment and infrastructure. Responsibilities include performing preventive maintenance activities, diagnosing equipment failures, and suggesting improvements to maintenance processes. The role requires a technical high school degree, experience in equipment maintenance, and basic computer skills. The company offers benefits such as organized transport, training programs, and various bonuses.

This role defines, governs, and enables visual and design standards for content across Emerging Markets, focusing on creating scalable, reusable, and high-quality content. It aims to improve efficiency, brand consistency, and usability by treating design as a system capability and optimizing content for reuse across various platforms.

Senior Manager, Field Medical, MD at Pfizer responsible for providing therapeutic area and product expertise, scientific exchange, medical engagement, customer insights, and research support within assigned geographies. The role involves delivering accurate medical information, supporting research, and acting as a medical resource to internal and external stakeholders, contributing to medical strategy through patient-focused, data-informed scientific exchange.

Senior Manager, Field Medical, MD role at Pfizer, focused on providing therapeutic area and product expertise in assigned geographies. Responsibilities include scientific exchange, medical engagement with healthcare professionals, customer insights gathering, and research support. The role requires an MD degree and involves maintaining scientific knowledge, delivering medical information, and contributing to medical strategy through patient-focused, data-informed scientific exchange.

Senior Manager, Field Medical, non-MD role at Pfizer, focused on providing therapeutic area and product expertise across assigned geographies. Responsibilities include scientific exchange, medical engagement, customer insights, and research support, with a focus on healthcare professionals and organized customer segments. The role involves delivering accurate medical information, supporting research, and serving as a medical resource.

Senior Manager, Field Medical, non-MD role at Pfizer, responsible for providing therapeutic area and product expertise, scientific exchange, medical engagement, customer insights, and research support to healthcare professionals and organized customers. The role involves delivering accurate medical information, supporting research, and identifying gaps between evidence-based care and real-world practice.

Pfizer is seeking a Clinical and Translational Biomarker Lead to develop and implement biomarker strategies for assigned assets in weight management and cardiometabolic disease. This role involves scientific and technical leadership, managing external and internal partners for biomarker assays and data, and contributing to clinical development plans, regulatory filings, and publications. The lead will oversee assay lifecycle management, manage external laboratories, and interpret biomarker results in the context of clinical studies.

The Field Medical Director role at Pfizer focuses on providing therapeutic area and product expertise to medical customers within a designated territory. Responsibilities include delivering approved medical content, engaging with healthcare professionals (HCPs), supporting clinical trial site identification, and providing insights on disease states and patient needs. This role requires strong scientific knowledge, communication skills, and the ability to collaborate within a matrixed environment.

Pfizer is seeking a Director-level Clinical Development Scientist for their Oncology portfolio. This role involves scientific oversight, data integrity, and quality of clinical trials, partnering with cross-functional teams, authoring study documents, and analyzing emerging safety and clinical data. Requires extensive experience in clinical research, particularly in Phase 3 Oncology trials, and a strong understanding of regulatory guidelines.

This role is for a Senior Manager in Oncology Clinical Development at Pfizer, responsible for scientific oversight, data integrity, and quality of clinical trials. The position involves authoring protocols, reviewing clinical data, analyzing safety profiles, and ensuring compliance with regulations and SOPs. It requires a strong background in clinical research within the oncology space, experience with large datasets, and collaboration with cross-functional teams.

Oncology Field Medical Director role focused on providing therapeutic area and product expertise to customers in an assigned territory, managing medical strategy, and serving as a conduit for medical information and customer insights. Requires an MD/DO degree and expertise in breast or gynecologic oncology.

Student position in Zagreb, Croatia, focusing on sampling and testing in a production environment. Responsibilities include collecting microbiological samples, checking physical parameters, sampling raw materials and energy sources, receiving samples, issuing analysis results, maintaining documentation, and participating in equipment qualification/validation. Requires availability 3 days a week, including weekends, with advanced English and MS Office skills. Preference for biotech, chemical, pharmaceutical, veterinary, or health-related fields.

Medical Director providing Clinical Development leadership for late-phase Hematology clinical trials, overseeing design, conduct, and analysis. Collaborates with cross-functional teams (regulatory, pharmacovigilance, biostatistics, medical affairs) and external stakeholders to ensure scientific, ethical, and regulatory standards are met. Responsibilities include medical monitoring, data review, safety monitoring, investigator interactions, and contributing to clinical and regulatory documents. Provides strategic guidance and interprets clinical data.

Pfizer is seeking a Director, Health Technology Assessment (HTA), Value & Evidence (HV&E) for their Obesity portfolio. This role will lead the development and execution of global evidence generation strategies, including HEOR studies, to ensure optimal patient access to treatments. The Director will collaborate with cross-functional teams and external experts to inform healthcare decision-making and support reimbursement requirements.

Pfizer is seeking a Director, HTA, Value & Evidence (HV&E) to support the strategic goals of the Internal Medicine Division by driving optimal patient access for early pipeline obesity and non-obesity products. This role involves formulating HEOR strategy, overseeing evidence generation activities (RWD studies, economic models), and preparing for Phase 3. The Director will lead the development and execution of global evidence generation strategies, including HEOR studies and patient-reported outcomes, and partner with internal and external stakeholders to ensure appropriate dissemination of HEOR materials and support asset strategies.

Pfizer is seeking an Oncology Field Medical Director (MD) with expertise in genitourinary (GU) oncology to provide therapeutic area and product knowledge to customers within an assigned territory. The role involves executing medical strategy, serving as a conduit for medical information, collaborating with internal teams on clinical trial identification, and supporting research initiatives. The position requires an MD or DO degree, strong communication and interpersonal skills, and the ability to travel extensively.

Pfizer is seeking an Oncology Field Medical Director (MD) with expertise in genitourinary (GU) oncology to provide therapeutic area and product knowledge to customers in an assigned territory. The role involves planning and executing medical strategy, serving as a conduit for medical information, identifying potential clinical trial sites, and collaborating with internal and external stakeholders. The position requires an MD or DO degree, 4+ years of relevant experience, and strong communication and interpersonal skills, with significant travel required.

Pfizer is seeking a GU Oncology Field Medical Director to provide therapeutic area and product expertise in genitourinary oncology across assigned territories. The role involves planning and executing medical strategy, engaging with customers, serving as a resource for medical information, and collaborating with internal teams on medical content and clinical trial identification. The position requires strong communication and interpersonal skills, with a focus on patient centricity and compliance.

This role is for a Director of Oncology Field Medical Outcomes, focusing on engaging with payers and integrated customers to educate them on the clinical and economic impact of Pfizer's Oncology medicines. The role involves analyzing real-world data, pharmacoeconomics, and outcomes to improve patient care and population health, with a strong emphasis on Health Information Technology (HIT) and clinical informatics.

Administrative Lead role providing comprehensive administrative support to the Chief Development Officer within Inflammation & Immunology Development at Pfizer. Responsibilities include calendar management, meeting coordination, travel logistics, expense reporting, and ensuring adherence to company policies and compliance requirements. The role requires independent work, prioritization, and managing multiple tasks in a fast-paced global organization. Interaction with senior leaders, scientists, clinicians, and collaborators is expected.

The Specialty Care Field Medical Director provides therapeutic area and product expertise to external medical stakeholders in an assigned territory. Responsibilities include planning and executing medical strategies, maintaining knowledge of disease states and medicines, serving as a conduit for medical information and insights, developing medical educational content, and ensuring all activities comply with Pfizer policies and guidance. The role involves educating stakeholders on disease states and care guidelines to improve patient outcomes, identifying potential sites for clinical trials, and supporting the Investigator Sponsored Research process. The candidate must have an MD or DO degree, relevant experience, strong leadership, communication, and interpersonal skills, and the ability to manage projects in a remote, matrixed environment.

Clinical Development Medical Director at Pfizer responsible for medical and scientific oversight, data integrity, and quality of clinical trials in Internal Medicine. This role involves providing medical monitoring, contributing to protocol design, ensuring regulatory compliance, and potentially managing other clinical colleagues. Requires a medical degree and significant experience in biopharmaceutical clinical research and development.

This role is for a Specialty Care Field Medical Director at Pfizer, responsible for providing therapeutic area and product expertise to external medical stakeholders within an assigned territory. The role involves planning and executing medical strategies, maintaining knowledge of disease states and medicines, serving as a conduit for medical information and insights, and contributing to medical educational content strategy. It also includes educating stakeholders on disease states and care guidelines, identifying sites for clinical trials, and supporting Investigator Sponsored Research. The position requires strong leadership, communication, and interpersonal skills, with a focus on optimizing patient care and adhering to all company policies and compliance guidance.

Clinical Development Medical Director (Associate Director) at Pfizer responsible for medical and scientific oversight, data integrity, and quality of clinical trials in Internal Medicine. This role involves providing medical monitoring, clinical support, protocol design input, and contributing to regulatory filings and reporting.