Pfizer

This role is a Medical Affairs Specialist (MAS) at Pfizer in Japan, focusing on Oncology and Hematology. The primary responsibilities include serving as a scientific point of contact for healthcare professionals and external stakeholders, providing and exchanging medical/scientific information, contributing to local medical strategies, and developing/executing medical plans. The role involves collaborating with stakeholders, managing unsolicited medical requests, and gathering/analyzing medical insights to address unmet medical needs and ensure the safe and effective use of products. It requires maintaining high scientific standards and compliance in all activities.

This role is a Medical Affairs Scientist (MAS) at Pfizer Japan, focusing on Gastroenterology. The primary responsibilities include serving as a medical scientific point of contact for healthcare professionals and external stakeholders, providing and exchanging medical/scientific information, contributing to local medical strategies, and developing/executing medical plans. The role involves identifying unmet medical needs, conducting scientific exchanges, managing unsolicited medical requests, supporting investigator-sponsored research and medical grants, and generating real-world evidence. The goal is to foster strong scientific relationships and ensure the safe and efficacious use of Pfizer's products.

Develops and implements market access strategies for new pharmaceutical assets, focusing on pricing, reimbursement, and ensuring optimal patient access. This involves deep stakeholder analysis, cross-functional team leadership, and strategic planning to support product launch and long-term potential.

Manager/Sr Manager, Pricing & External Affairs at Pfizer in Japan, responsible for developing and executing pricing strategies for new drugs, leading negotiations with MHLW, and shaping pro-innovation pricing frameworks. Requires deep understanding of Japanese healthcare systems and pricing rules, strategic thinking, and strong communication/negotiation skills.

Responsible for in-country study/site management and clinical/scientific oversight of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable laws, GCP, and Pfizer standards. This role involves leading and coordinating trial execution, managing investigator site relationships, and ensuring timely communication between global and local study teams. Requires excellent Japanese and English communication skills.

Pfizer is seeking a Japan Study Manager to oversee and manage clinical trials in Japan. This role involves collaborating with CROs and clinical sites to ensure patient safety, data quality, and adherence to GCP and Pfizer standards. Responsibilities include study start-up, monitoring, issue resolution, and communication between global and local teams. Requires strong study and site management experience, knowledge of GCPs, and excellent Japanese and English communication skills.

Perform environmental monitoring in a safe, compliant, and efficient manner within Pfizer's Aseptic Manufacturing Environment to ensure product quality. Responsibilities include sampling, data entry, report authoring, supply management, aseptic gowning, and documentation practices, adhering to cGMP, GLPs, and EHS standards.

Manager for Flexible Resource Strategy at Pfizer, focusing on vendor management and contracting for Clinical Development and Operations (CD&O) and other R&D functions. The role involves partnering with internal customers to identify resourcing options, manage sourcing and contracting efforts, and ensure compliance with business requirements. Experience with drug development phases and contracting/budgeting models is required. Familiarity with AI tools like ChatGPT and Microsoft Copilot is a plus.

Seeking a Principal Scientist for Downstream Process Development in Bioprocess R&D. The role involves hands-on laboratory research to develop and optimize recovery and purification processes for recombinant proteins, supporting clinical programs. Responsibilities include designing studies, analyzing data, contributing to process characterization and validation, authoring reports, and providing technical leadership.

The role of Utilities Leader at Pfizer's Buenos Aires plant is responsible for ensuring the availability of plant utility equipment and managing the electrical system. This includes participating in technical specifications for new equipment, planning corrective/preventive/predictive maintenance, reporting deviations, and ensuring compliance with cGMP and EHS standards. The role also involves managing the M&R budget, supervising technical staff, and collaborating with internal clients and corporate initiatives.

This role supports the design, development, implementation, and maintenance of stability protocols and studies for pharmaceutical products. Responsibilities include reviewing and assessing stability data, providing quality stability reports for regulatory submissions, and authoring stability sections of regulatory documents. The specialist will analyze stability data, identify and troubleshoot issues, and ensure compliance with cGMPs and relevant regulations (FDA, ICH).

This role is for an Aseptic Production Lead at Pfizer, responsible for overseeing and potentially leading lower-level staff in pharmaceutical manufacturing. The role involves managing personal time, contributing to projects, providing direction and training, problem-solving, adhering to standards and guidelines, monitoring equipment, and improving processes using Lean principles. It requires a high school diploma, 6+ years of experience, attention to detail, problem-solving skills, and the ability to work independently or in groups. Bonus points for a bachelor's degree, pharmaceutical manufacturing experience, and familiarity with AI tools.

This role is a Quality Lead responsible for supporting the evaluation, selection, development, qualification, and integration of new suppliers, partners, products, and contractors within Pfizer's pharmaceutical operations. It involves ensuring commercial readiness, conducting quality due diligence, managing quality agreements, and providing quality support for new product launches and technology transfers, all while adhering to strict regulatory compliance and quality systems.

Quality Assurance Supervisor role at Pfizer in Shanghai/Suzhou, focusing on implementing and maintaining quality management systems, conducting audits, managing product disposition, and ensuring supplier quality within the pharmaceutical industry. The role involves adherence to GxP, GMP/GDP, and local regulations, with a preference for licensed pharmacists and experience with AI tools for productivity.

This role is for a Junior Officer in Pharmaceutical Manufacturing at Pfizer, focusing on ensuring the availability of essential medications. Responsibilities include managing personal contributions, prioritizing workflow, completing assignments based on established procedures, identifying process improvements, troubleshooting issues, and training team members. The role requires hands-on experience with critical manufacturing machines and adherence to cGMPs and safety guidelines.

Operations Engineer at Pfizer Singapore responsible for analyzing and designing operational sequences and workflows to improve production facilities, ensuring compliance with regulations and Good Manufacturing Practices (GMP). The role involves process monitoring, safety and environmental improvements, process reliability, validation, technology transfers, cost control, and inventory management. Key activities include supporting plant operations for API manufacturing, collaborating on investigations, driving continuous improvement initiatives, ensuring EHS and GMP compliance, executing production and maintenance activities, troubleshooting processing issues, and participating in commissioning and validation.

Manager, Market Access at Pfizer in India responsible for shaping and executing access strategies within public and private healthcare ecosystems. This involves understanding reimbursement pathways, building partnerships, and supporting health economics and evidence strategy to drive adoption of innovative therapies and adult vaccination programs.

Pfizer Singapore is recruiting for a Process Development Scientist to support manufacturing site expansion. The role involves analyzing and designing operational sequences and workflows to improve production facilities, ensuring compliance with regulations and Good Manufacturing Practices. Responsibilities include process monitoring, safety and environmental improvements, process reliability, validation, technology transfers, cost control studies, and developing implementation plans. The scientist will also contribute to project milestones, provide technical expertise, review process data, solve problems, support training, manage efforts for short-term goals, and maintain laboratory operations. The role requires a Bachelor's Degree, leadership/process experience, laboratory experience, basic technical knowledge, strong organizational and documentation skills, effective communication, and proficiency in Microsoft Applications. Core competencies include teamwork, organic synthesis, analytical chemistry, and technical writing.

This role focuses on microbiological testing and quality control within a pharmaceutical setting, ensuring the safety and efficacy of products. Responsibilities include media preparation, various microbiological tests, data interpretation, documentation compliance, and procedure review. The role requires a Master's degree in microbiology or biotechnology with 4-7 years of experience, strong technical skills in method validation and testing, and knowledge of GMP/GLP.

Pfizer is offering a 15-month Career Progression Program (CCP) for fresh graduates or mid-career professionals in Singapore to develop skills in biopharmaceutical manufacturing. The program includes training on manufacturing instructions, process control systems, quality and EHS investigations, process improvements, and team collaboration. A degree in Engineering (Chemical preferred) or Science (Chemistry major) is required.

Administrative Lead role at Pfizer, focusing on supporting senior leaders and large teams. Responsibilities include meeting management, travel coordination, budget tracking, recruitment support, document preparation, vendor management, and employee engagement activities. Requires at least 7 years of experience as an administrative professional and proficiency in Microsoft Office. Familiarity with AI tools is a plus.

Group Manager for Quality Control at Pfizer in India, responsible for leading QC teams, overseeing analytical activities (in-process, finished product, stability), managing equipment qualification and calibration, ensuring compliance with cGMP and regulatory requirements, and driving continuous improvement. The role requires extensive pharmaceutical industry experience in QC, with a focus on people management, laboratory operations, and quality systems.

This role is part of a training program focused on operational effectiveness within biopharmaceutical manufacturing. The specialist will lead and coach using Lean and Six Sigma methodologies, deploy an Integrated Manufacturing Excellence (IMEx) 'way of working', and contribute to site performance and continuous improvement. Responsibilities include training colleagues, guiding Green and Yellow Belts, measuring site performance, leading problem-solving initiatives, managing projects for site stabilization, and tracking performance metrics.

Lead digital and automation capabilities at a manufacturing site, focusing on strategy, portfolio ownership, operational reliability, compliance, and people leadership within a regulated healthcare environment.

The Senior QC Lab Manager at Pfizer in Singapore will oversee Quality Control laboratory services and teams, ensuring compliance with GLPs, GDPs, cGMPs, and Pfizer Quality Standards. Responsibilities include leading analytical testing, data review, equipment management, quality systems, personnel management, budget development, and ensuring a safe working environment. The role involves collaborating with various site functions and managing analytical method transfers and product stability programs.

This role is for a Medical Advisor in the Oncology department at Pfizer in Shanghai, China. The primary responsibilities include managing medical activities, ensuring scientific validity and ethics, enhancing local data generation, managing product lifecycle from a medical perspective, evaluating new products and research programs, developing post-marketing research strategies, providing direction for Phase IV studies, designing and managing local Non-interventional Studies (NIS), developing and implementing medical strategy, developing and implementing publication plans, evaluating Investigator-Initiated research proposals, providing medical input on business decisions, co-developing product strategy and messaging with marketing, providing medical support for marketing activities, developing medical insight documents for business partners, reviewing and approving local standard response letters to HCPs, developing training programs for sales force, supporting drug registration activities (labeling, medical justification, feasibility evaluation, site selection, protocol synopsis, study report), academic communication with KOLs and medical societies, crisis management, providing expert opinion in safety events management, and ensuring medical compliance. The role requires a clinical medicine background, master's degree or above, 3 years of clinical practice in Tier 3 hospitals or medical affairs experience, and fluency in English.

Administrative Assistant role at Pfizer, supporting business leaders with comprehensive administrative tasks, process improvements, and logistics. Requires a Bachelor's degree, 5+ years of experience, and proficiency in Microsoft Office. Preferred experience includes supporting executive leadership, knowledge of the pharmaceutical industry, and experience with AI tools like ChatGPT or Copilot.

Associate Director, Research and Development for Vaccines at Pfizer in Japan. This role involves providing medical and scientific expertise for clinical trials, contributing to protocol design and development strategy, ensuring patient safety across studies, and interacting with regulatory authorities and key opinion leaders. The position requires a medical degree and licensing, with a focus on the Japan and Asia-Pacific regions.

The Data Manager is responsible for the timely and high-quality review and query management of clinical data for Pfizer's portfolio. This role involves executing key data management deliverables to ensure the integrity of clinical data, including data acquisition standards, database design, data review, query management, data access and visualization, metrics reporting, database release, and submission activities. The Data Manager will collaborate with Clinical Data Scientists to ensure operational excellence and adherence to SOPs and working practices, ensuring high-quality CDIS documents for inspection and submission readiness.

This role is responsible for executing transactional HR activities related to the Colleague Life Cycle, excluding recruitment. It involves processing changes, administering leave, supporting benefits and compensation, HR reporting, and internal controls. The role also focuses on process improvement and service enhancement, supporting colleagues with inquiries, liaising with other teams, and running reports. A basic qualification is at least 1 year of experience in HR Shared Services or a similar customer service environment, with strong attention to detail and customer focus. Preferred qualifications include knowledge of AI and automation tools like Microsoft Power Automate, experience with HR systems like Workday or Service Now, and familiarity with payroll software.

Lead cloud platform operations for availability, reliability, security, and cost efficiency across enterprise cloud environments (AWS, Azure, GCP). Drive automation-first practices, incident management, SRE principles, and ensure compliance with security and regulatory requirements. Manage operational teams and partner with engineering and security.

This role focuses on content management within Pfizer's Emerging Markets Content Catalyst Center of Excellence. The primary responsibilities include ensuring content integrity, governance, reuse readiness, and operational excellence across the entire content lifecycle. The role acts as a guardian of content systems, metadata, and scientific accuracy to improve time-to-market, reuse rates, and compliance. It involves managing content submission and approval processes, analyzing performance, and supporting the adoption of new technologies, including AI-enabled workflows.

Undergraduate placement role in Pfizer's Global Hospital & Biosimilars Commercial team, focusing on portfolio management, commercial marketing, and supply chain operations for established brands and biosimilars. The role involves stakeholder management, project implementation, and data-driven value proposition development within the hospital medicines market.

Student position in Zagreb, Croatia, assisting with the processing and administration of training materials, product complaint handling, trend analysis, and computer work. Requires students from chemistry, biotechnology, pharmacy, or veterinary fields, with excellent English and Croatian, proficiency in MS Office, and availability for full-time work. Candidates should be in their final years of study, responsible, adaptable, systematic, precise, and team players.

This role supports the quality of medical activities, audit/inspection readiness, and risk mitigation across therapeutic areas for Pfizer's Medical Affairs and National Medical Operations. It involves ensuring compliance with regulatory standards, managing quality events, and participating in inspections and audits.

Pfizer is seeking an Apprentice Process Technician for their biopharmaceutical manufacturing plant in Dublin, Ireland. This 2-year program combines part-time learning with work placement, leading to a Higher Certificate in Bio Process and Chemical Process Technician. The role involves assisting with routine production activities, equipment preparation, material handling, in-process checks, and supporting sampling and validation activities within a cGMP environment. The position requires a strong work ethic, commitment to compliance, and willingness to work shifts.

Lead the supply chain for investigational products in clinical studies, overseeing matrix teams, managing budgets, identifying risks, and ensuring delivery from API to clinical sites. This role involves developing global supply strategies, collaborating with study teams, and ensuring quality and regulatory compliance.

This role is a Microbiology Leader at Pfizer, responsible for ensuring the microbiological quality control of products, raw materials, and packaging materials. It involves planning and implementing quality programs, managing laboratory personnel, ensuring compliance with GMP and EHS regulations, validating microbiological processes, and managing budgets. The role also focuses on data integrity and continuous improvement within the laboratory setting.

Responsible for disposition of API and API intermediates, including review of completed batch production and laboratory control records, ensuring deviations are investigated and resolved. Focuses on quality and compliance within a pharmaceutical setting.

This role is responsible for the programming of high-quality clinical databases, supporting assigned segments of the Pfizer portfolio. Accountabilities include the design, development, and maintenance of clinical databases, ensuring data integrity and applying standards for consistency in asset/submission data. It involves close collaboration with study team members to create data capture solutions and ensuring compliance with SOPs and work practices.

Duales Studium Business Administration/International Industrial Management (B.A.) at Pfizer in Berlin, starting 1.9.2026. The program combines theoretical studies at HWR Berlin with practical experience in various Pfizer departments (Marketing, Sales, IT, Finance, HR, etc.). It focuses on international business and industrial management, with most coursework in English. The program lasts 3 years and offers an attractive salary, opportunities for international experience, and a comprehensive benefits package. Requires (Fach-)Abitur with good grades in German, Math, and English, an interest in business and the pharmaceutical industry, MS Office skills, strong communication abilities, and teamwork skills.

The GSC Market Logistics Specialist is responsible for operational accountability of Market Logistics activities in the Irish market, coordinating material movement, managing inventory, overseeing import/export compliance, managing logistics service providers, and controlling the logistics budget. The role focuses on ensuring efficient flow of products to meet customer requirements within financial constraints and driving continuous improvement of logistics processes.

This role is for a Medical Affairs Scientist at Pfizer, focusing on building relationships with healthcare professionals and stakeholders to advance patient outcomes. The scientist will generate and share medical insights, manage external engagements, and collaborate with internal teams. The role requires an advanced scientific degree and pharmaceutical experience, with a strong emphasis on stakeholder management and compliance within the healthcare and pharmaceutical industry.

Marketing internship in Immunology and Inflammation at Pfizer, supporting marketing managers and cross-functional teams on a dynamic product portfolio. The role involves developing omnichannel activities and solutions for healthcare professionals, working with various departments, and creating promotional and digital materials for mature, launching, and developing products.

This role is responsible for sample logistics within Pfizer's Vaccines R&D, involving receiving, tracking, documenting, storing, aliquoting, distributing, and disposing of samples from clinical trials according to approved protocols and GxP/regulatory requirements. It includes using electronic databases and robotic instruments for sample handling and distribution.

Pfizer is seeking a Young Graduate Automation Engineer for a two-year program in Puurs, Belgium. The role involves rotations through Process Automation, Technology & Systems, and Data Science & Software Development, focusing on industrial automation solutions like PLC and SCADA systems. The program aims to build a broad engineering foundation with intensive guidance and coaching, leading to a permanent role.

This role focuses on developing synthetic routes and scalable chemical processes for novel small molecule components in targeted therapeutics within the pharmaceutical industry. It involves route scouting, process development, and characterization, applying principles of organic chemistry and process research. The role also includes mentoring junior scientists, leading cross-functional teams, and overseeing GMP production batches.