Pfizer

This role focuses on managing supply planning activities to ensure reliable product supply, leveraging digital tools and automation. While it involves using AI tools like ChatGPT for problem-solving and productivity enhancement, the core function is supply chain management, not the direct development or deployment of AI models. The role emphasizes data analytics, scenario analysis, and cross-functional collaboration within a supply chain context.

This role focuses on delivering financial analytics, dashboards, and reporting using visualization tools like Power BI. It involves analyzing financial data, ensuring data accuracy, and supporting the adoption of modern analytics capabilities. The role will apply AI-enabled tools responsibly to enhance reporting efficiency, but the core function is finance analysis and reporting, not AI/ML model development.

The Associate MQA Downstream role at Pfizer is responsible for ensuring quality and compliance with cGMP standards in pharmaceutical manufacturing processes, specifically in Terminal Sterilization, Visual Inspection, and Packing areas. This involves reviewing batch records, performing inspections, monitoring processes, and identifying areas for improvement to ensure product safety and patient care.

This role is responsible for executing content management of non-complex local product documents, local label documents, and patient leaflets for nationally registered products. It involves system management for labeling activities, QC of labeling text, and ensuring data integrity. The role requires basic knowledge of labeling and regulatory principles, proficiency in systems, and experience with structured data. Experience in Regulatory Affairs, particularly with product labeling and regulatory guidelines, is important.

Associate role in pharmaceutical manufacturing at Pfizer, focusing on supporting production processes, problem-solving, and ensuring quality and adherence to standards. Requires a High School Diploma/GED and 2+ years of experience, with bonus points for cGMP experience and familiarity with AI tools.

This role supports the Quality Organization by ensuring compliance with regulatory requirements, company quality systems, and cGMP. It focuses on continuous improvement, project leadership, and cross-functional partnerships to enhance compliance, efficiency, and inspection readiness in a pharmaceutical manufacturing environment.

Pfizer is seeking a Policy Manager for Argentina to design and implement public policy initiatives focused on strengthening the public market. This role involves leading complex projects in public health contexts, collaborating with technical teams, managing strategic relationships with patient associations and civil society organizations, and ensuring compliance. The manager will also promote innovative approaches, including the use of digital tools, analytics, and AI, and identify opportunities for scaling successful initiatives.

Pfizer is seeking a Clinical Development Medical Director to serve as a clinician within a vaccine development program. This role involves providing medical and scientific expertise and oversight for clinical trials, ensuring patient safety, contributing to protocol design and strategy, supporting study teams, and interacting with regulatory authorities and key opinion leaders. The position requires accountability for the medical and scientific validity of study reports and disclosures.

Administrative Lead role supporting the VP, Head of Agent Product Management at Pfizer. Responsibilities include calendar management, meeting coordination, travel arrangements, expense reporting, and supporting AI events. Requires strong organizational and communication skills, with a demonstrated aptitude for learning and applying AI tools.

The role is for a Pharmacist as a Process Manager in Product and Process Development at Pfizer in Germany. The responsibilities include overseeing development and transfer activities for solid dosage forms, ensuring compliance with safety, environmental, and GMP regulations, and maintaining the pharmaceutical quality of clinical and regulatory test samples. The role also involves project management, tech transfer coordination, and supporting manufacturing sites with transfer activities. A degree in pharmacy or a related field, experience in drug development or production, and fluency in German and English are required.

Pfizer is seeking a Senior Director of Clinical Development Scientist to provide scientific oversight and ensure the quality of clinical trials in Internal Medicine. The role involves leading clinical execution, protocol development, data and safety review, and collaboration with various stakeholders including Health Authorities and KOLs. The position also requires managing clinical deliverables, ensuring TMF compliance, and potentially contributing to regulatory filings and publications. The role may also involve managing and mentoring other clinical colleagues.

Instrument Engineer role at Pfizer's biopharmaceutical manufacturing site in Strängnäs, Sweden. Responsibilities include developing, managing, and future-proofing plant instrumentation, ensuring compliance with quality standards and validated status. The role involves technical expertise, leading technical tasks, participating in qualification and deviation management, preventive maintenance planning, continuous improvement initiatives, and managing service agreements. Requires a technical degree or equivalent experience, expertise in instrumentation/metrology/electrical fields, understanding of measurement techniques and uncertainties, and experience in regulated environments (GMP is a plus). Strong communication skills in Swedish and English are necessary. The ideal candidate is structured, analytical, solution-oriented, responsible, and collaborative.

Director, Evidence Generation Systems at Pfizer, responsible for hands-on ownership, delivery, and evolution of core Evidence Generation systems within a regulated healthcare environment. The role involves translating business priorities into system designs, driving delivery across platforms, and resolving integration and compliance challenges. Focus on strategy execution, system modernization, and ecosystem integration.

Senior Regulatory Associate at Pfizer in the UK, responsible for obtaining and maintaining Marketing Authorizations and supporting Clinical Trial Applications for assigned products and markets. This role involves strategic regulatory activities, providing advice, managing applications and renewals, responding to regulatory authority queries, and ensuring compliance with legal requirements. It requires a life sciences or chemistry graduate with proven experience in Regulatory Affairs for Human Medicinal Products.

Lead people, technology, and financial resources in pharmaceutical manufacturing to achieve desired outcomes, ensuring adherence to SOPs, GMPs, and plant protocols. Manage investigations, corrective actions, and team performance while fostering continuous improvement and compliance.

This role is for a Senior Project Manager at Pfizer's Innovation Centre in Hangzhou, China. The primary responsibility is to manage the full lifecycle of digital solutions projects for doctors and patients, ensuring successful completion within established objectives, budgets, and timelines. The role involves coordinating with cross-functional teams, managing project compliance risks, and reporting on project status. It requires strong project management experience, organizational skills, and the ability to drive project progress and achieve business objectives.

Pfizer is seeking an Engineering Maintenance Technician in Dublin, Ireland, to manage maintenance and reliability engineering activities for utilities, buildings, and equipment. The role involves providing engineering support for project execution, operational support, reviewing work orders, conducting Root Cause Failure Analysis (RCFA), ensuring calibration compliance with Good Manufacturing Practices (GxP), and assisting in the development of the Preventative Maintenance program. The ideal candidate will have a Diploma/Degree in an Engineering/Technical Discipline or Electrical/Mechanical Trade Qualification, 3+ years of experience, and strong troubleshooting skills in mechanical and electrical systems, with desirable experience in commissioning, qualification, start-up, and process automation systems.

This role is for a Group Manager focused on Inspection Readiness within Pfizer's pharmaceutical operations in India. The primary responsibilities include managing the Site Quality Review program, overseeing CAPA management, ensuring compliance with regulations and GMP, and coordinating with global teams for inspection preparation. The role requires strong knowledge of pharmaceutical manufacturing, quality systems, and people management, with a minimum of 10 years of experience in the industry.

This role manages the process of creating and updating labeling artwork for pharmaceutical packaging, ensuring compliance with regulatory requirements and coordinating with various internal and external stakeholders. It involves initiating artwork requests, tracking changes, managing timelines, and ensuring accurate final content for product packaging.

Senior Manager, MAPP Technical Lead at Pfizer, responsible for the end-to-end architecture strategy of the MAPP compliance platform, ensuring alignment with business objectives and adherence to privacy and data protection requirements. This role involves guiding development teams, ensuring compliance with security and data governance frameworks, and identifying platform improvement opportunities.

Pfizer is seeking a Director of Vaccines Clinical Research (MD required) to provide medical and scientific expertise for clinical trials, ensuring patient safety and overseeing study design, execution, monitoring, delivery, and reporting. The role involves designing development strategies, participating in committees, reviewing compounds for in-licensing, and supporting new business development. Responsibilities include managing safety surveillance, protocol design, study team support, data interpretation, regulatory document authorship, and interactions with regulatory authorities, key opinion leaders, and principal investigators.

Pfizer is seeking a GU Oncology Field Medical Director to provide therapeutic area and product expertise in genitourinary oncology across assigned customers and initiatives within a territory. The role involves planning and executing medical strategy, maintaining knowledge of oncology and Pfizer medicines, serving as a resource for medical information, contributing to medical content strategy, and collaborating with internal and external stakeholders. Responsibilities include delivering approved medical content, identifying and engaging priority customer segments, responding to unsolicited medical requests, supporting clinical trial site identification, providing medical support for Investigator Sponsored Research, cultivating research expertise, and representing Pfizer Medical Affairs at professional associations.

This role is for a Senior Production Operator at Pfizer, responsible for operating, maintaining, and troubleshooting pharmaceutical manufacturing equipment. The position requires experience with cGMP, SOPs, and safety protocols, with a focus on ensuring production quality and efficiency. It involves hands-on mechanical work, data interpretation from control systems, and training new hires. The role is critical for delivering medicines to patients.

Senior Manager, Global Medical Affairs for Obesity will provide support for the Global Obesity Medical strategy to achieve short- and long-term Medical objectives in alignment with the overall business strategy. The incumbent is an integral member of the Global Medical team, supporting ongoing and new Medical initiatives to enable productive internal cross-functional and external professional partnerships.

Medical Science Liaison (MSL) role focused on vaccines, involving customer-facing medical education, scientific information dissemination, customer engagement, and collaboration to improve patient outcomes. The role requires strong communication, analytical, and organizational skills, with an understanding of pharmaceutical industry codes and local regulations. Experience in the vaccine therapeutic area is preferred.

Supervisor responsible for leading downstream production of mAb products, ensuring targets, quality, compliance, cost standards, and customer service are met. This includes managing staff, planning, performance assessment, and employee counseling. Ensures work is accurate, timely, efficient, and compliant with corporate policies, SOPs, cGMP, and FDA regulations. Participates in investigations and continuous improvement initiatives using LEAN and Six Sigma. Optimizes resources for maximum production and ensures quality and safety standards.

Supervisor for downstream operations of mAb products in pharmaceutical manufacturing, focusing on production targets, quality, compliance, and team management. Ensures adherence to cGMP and FDA regulations, optimizes resources, and leads production staff.

Administrative Partner role at Pfizer supporting the Oncology Medical Head, Hematology. Responsibilities include calendar management, meeting coordination, travel logistics, expense reporting, and handling confidential correspondence. Requires strong organizational, communication, and problem-solving skills, with proficiency in Microsoft Office Suite. Experience with AI tools like ChatGPT is a plus.

Administrative Lead role at Pfizer, providing comprehensive support to business leaders, managing records, scheduling, implementing process improvements, and organizing logistics for meetings. Requires a High School Diploma/GED with 6 years of experience, proficiency in Microsoft Office, and strong organizational and communication skills. Preferred experience includes supporting executive leadership in a global organization, pharmaceutical industry knowledge, and experience with AI tools like ChatGPT or Copilot for productivity enhancement.

This role is for an Assistant Associate in Engineering Stores at Pfizer, responsible for managing material receipts, storage, and issuance within the manufacturing logistics and supply team. The position involves using systems like SAP MM/EAMS/ARIBA, adhering to cGMP and safety procedures, and ensuring efficient material flow to support patient access to medicines. Key duties include inventory management, documentation, and supporting audits.

Manager for Indirect Taxation in India, responsible for hands-on management and execution of GST, Customs, and EOU-related compliances for a large multinational pharmaceutical organization. The role involves supporting the Taxation Lead in compliance, audits, reconciliations, litigation support, and regulatory interactions, ensuring timely and accurate filings and adherence to evolving tax laws.

The Specialty Care Field Medical Director, MD at Pfizer is responsible for providing therapeutic area and product expertise to external medical stakeholders in an assigned territory. This 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. The director will also identify potential sites for Pfizer-sponsored clinical trials and support the Investigator Sponsored Research (ISR) process. The role requires an MD or DO degree and at least 4 years of relevant experience, with strong scientific communication, interpersonal, and leadership skills.

The Hematology Field Medical Director at Pfizer is responsible for providing therapeutic area and product expertise in malignant hematology and pipeline to various medical customer segments within an assigned territory. This role involves planning and executing medical strategy, maintaining knowledge of the therapeutic area and Pfizer medicines, serving as a conduit for medical information, and collaborating with internal and external stakeholders. The position requires strong communication skills, the ability to manage projects remotely, and significant travel.

This role focuses on providing therapeutic area and product expertise to external medical stakeholders within a designated territory. Responsibilities include planning and executing medical strategies, maintaining knowledge of diseases and medicines, serving as a conduit for medical information and insights, and educating stakeholders on disease states and care guidelines. The role also involves collaborating with internal teams on medical content strategy, clinical trial site identification, and supporting investigator-sponsored research. It requires strong scientific communication, leadership, and interpersonal skills, with a focus on optimizing patient care.

Pfizer is seeking an Oncology Field Medical Director with expertise in Malignant Hematology to provide therapeutic area and product knowledge to healthcare professionals in an assigned territory. The role involves executing medical strategy, serving as a conduit for medical information and customer insights, supporting clinical trial identification and the Investigator Sponsored Research process, and collaborating with internal and external stakeholders.

Senior QC Laboratory Analyst at Pfizer responsible for performing and reviewing analytical testing of raw materials, API samples, and in-process samples. The role involves adhering to cGMPs, ALCOA principles, and Data Integrity requirements, troubleshooting laboratory issues, and contributing to continuous improvement activities within a regulated healthcare environment.

This role is a Regional CET Manager for CFC Training in China, responsible for delivering training programs directly in the field, identifying training needs, developing tailored solutions, and assessing employee knowledge and skills. The role also involves contributing to the Regional Manager Leadership Team and reporting on training activities.

This role is for a Medical Information Communication Specialist at Pfizer in China. The primary responsibilities include academic promotion of products and professional support to customers within a designated region, under the guidance of a regional manager. Key tasks involve visiting clients, communicating product information, organizing academic events, collecting and analyzing market feedback, and maintaining communication with internal and external stakeholders. The role requires a college degree in a relevant field (medicine, pharmacy, life sciences preferred), proficiency in MS Office, good English, strong communication and teamwork skills, and a willingness to learn and self-motivate. Prior pharmaceutical industry experience is preferred. A strong emphasis is placed on compliance with company policies, industry standards, and anti-corruption laws like FCPA.

This role is for an Associate, Talent Acquisition at Pfizer in the Philippines, responsible for full-cycle recruitment from entry-level to Manager roles. The position involves managing end-to-end recruitment, stakeholder management, and ensuring a positive candidate experience. Key responsibilities include sourcing, selection, offer development, process compliance, and utilizing AI tools to enhance efficiency. The role requires strong organizational, communication, and problem-solving skills, with a preference for experience in the pharmaceutical industry and ATS platforms.

Seeking a Social Media Operations Manager for prescription drug initiatives, focusing on strategy, KOL/KOC collaboration, content creation, and strict adherence to pharmaceutical regulations. The role requires a blend of creativity and analytical skills to drive engagement and ensure brand compliance.

This role provides regulatory support for pharmaceutical products throughout their lifecycle, from initial registration to withdrawal. It involves managing regulatory dossiers, responding to health authority queries, and coordinating cross-functional activities for tenders, reporting, and launch planning. The position requires strong organizational skills, technical aptitude, and proficiency in Korean and English.

This role is a Health Care Executive at Pfizer in India, responsible for achieving sales budgets in an assigned geographical territory. Key responsibilities include developing sales strategies, conducting sales analytics, managing customer relationships (medical practitioners, chemists, wholesalers), delivering promotional messages, booking orders, preparing reports, and coordinating with internal teams. The role also involves managing product samples, promotional materials, and adhering to company policies and procedures. While the role mentions using technology for better information and effective field operations, it does not involve direct AI/ML development or application.

This role is for a Medical Information Communication Supervisor at Pfizer in Beijing, China. The primary responsibilities include providing product information and support to customers, visiting clients, communicating medical information, organizing events, and achieving business objectives. The role also involves coaching junior specialists, managing key accounts, and contributing to regional projects and platforms. The ideal candidate will have a strong background in the pharmaceutical industry, excellent communication and teamwork skills, and a commitment to compliance and integrity.

This role is a Medical Information Communication Specialist at Pfizer in Beijing, China. The primary responsibilities include promoting products academically and providing professional support to customers within their assigned region. This involves visiting clients, communicating drug information, organizing academic promotion activities, collecting and analyzing market feedback, and maintaining effective communication with internal and external stakeholders. The role requires a university degree in a related field, proficiency in MS Office, good English, strong communication and teamwork skills, and a willingness to learn. Prior experience in the pharmaceutical industry and a strong understanding of compliance regulations (FCPA, etc.) are preferred. The core competencies emphasize professionalism, compliance, business acumen, customer engagement, execution, and self-development.

Senior QC Laboratory Analyst at Pfizer responsible for performing and reviewing analytical testing of raw materials, API samples, and in-process samples. The role involves adhering to cGMPs, ALCOA principles, and Data Integrity requirements, troubleshooting laboratory issues, and contributing to continuous improvement activities within a regulated healthcare environment.

This role is for a Senior Medical Science Liaison (MSL) in the Dermatology department for Guangzhou, China. The primary responsibilities involve maximizing the value of Pfizer products by developing KOL management strategies, establishing regional platforms, providing medical training to sales teams, and supporting business decision-making. The role also involves enhancing local data generation through investigator-initiated research and providing medical expert input in safety event management, all while ensuring company compliance.

This role at Pfizer is for a Medical Advisor in the anti-infective field, focusing on developing and executing medical strategies for products in China. Responsibilities include enhancing local data generation, providing medical input for business decisions, training sales forces, supporting drug registration, academic communication with Key Opinion Leaders (KOLs), crisis management, safety event management, and ensuring medical compliance. The role requires deep medical expertise in the therapeutic area and strong collaboration with various internal and external stakeholders.

The role of Senior Regional Medical Advisor in Guangzhou, China, focuses on maximizing the value of Pfizer products by developing KOL management strategies, establishing regional academic relationships, providing medical training to sales teams, and supporting product lifecycle management. It involves communicating scientific information, leading medical programs, generating local medical insights, and ensuring compliance with company policies and regulations. The position requires a clinical or medical background, strong therapeutic area knowledge, and experience in pharmaceutical business operations.