This role supports the planning and execution of customer innovation and transformation strategies within Pfizer's China Inflammation & Immunology (I&I) and Geographic Expansion (GE) Business Units. It involves managing digital platforms, driving business impact through stakeholder influence, aligning with digital strategy, supporting go-to-market transformation, building digital capability platforms, implementing digital initiatives, leveraging marketplace insights for multichannel marketing programs, developing digital operation plans, and managing digital data collection and training. The role requires a Bachelor's degree, diverse commercial experience, 1+ years in pharma marketing or digital marketing, and strong communication and project management skills.

Pfizer is seeking a Health Representative for their Oncology division in Kuala Lumpur, Malaysia. This role focuses on identifying and implementing effective engagement strategies (virtual and in-person) to maximize product demand and drive sales. The representative will build customer relationships, deliver targeted messaging using approved materials, leverage product and disease knowledge, and strategically deploy Pfizer resources. A Bachelor's degree and at least 4 years of sales experience are preferred, along with strong business acumen, analytical skills, and the ability to adapt to new technologies.

This role is for a Regional Medical Information Communication Manager at Pfizer in Taizhou, China. The primary responsibilities include managing regional business and product groups, setting performance and compliance goals, leading and developing a sales team, ensuring compliance with company policies and regulations, and achieving sales targets. The role requires at least 2 years of Pfizer sales experience or 3 years of sales experience in a similar foreign pharmaceutical company, with a proven track record of meeting or exceeding sales performance. Internal candidates with sales management experience are preferred. A strong emphasis is placed on compliance and ethical business practices.

The Manager will develop various types of medical affairs content, including abstracts, manuscripts, presentations, summaries, and multimedia formats. This involves researching, organizing, and interpreting medical information, collaborating with cross-functional teams (including generative AI groups), ensuring accuracy and compliance, and staying updated on content generation trends and technologies.

Manager, Japan Compliance role at Pfizer, responsible for overseeing the implementation of Pfizer’s compliance program, leading strategic initiatives to assess and mitigate global risks, and partnering with various functions. The role involves supporting risk management, business advisory, third-party risk management, and culture building, with a focus on integrating data- and AI-enabled approaches into compliance activities and assessing emerging technology risks.

Pfizer is seeking a Regional Medical Advisor in Jinan, China, to develop and execute regional medical development and life-cycle management strategies for inline products. This role involves establishing academic platforms, managing Key Opinion Leaders (KOLs), providing medical training to sales teams, driving regional business decisions, enhancing local data generation through Investigator-Initiated Research (IIR), managing safety events, and ensuring company compliance. The position requires a Master of Medicine or above, 3 years of clinical practice or medical affairs experience, and strong knowledge of the therapeutic area and pharmaceutical business.

This role is for a Regional Medical Advisor in Hematology Oncology in Beijing, China. The primary responsibilities include maximizing the value of Pfizer products through medical activities, implementing medical/research/disease management programs, conducting medical education, facilitating communication with healthcare providers and key influencers, and providing medical training to commercial teams. The role involves leading medical-to-medical communication, contributing to product strategy, supporting clinical research (non-interventional and investigator-initiated), implementing medical programs, and ensuring medical compliance.

The Associate Manager, Medical Communications and Content Solutions at Pfizer will develop medical affairs content, including abstracts, manuscripts, posters, and multimedia formats. Responsibilities include researching, compiling, and quality checking content, collaborating with internal teams, and ensuring adherence to quality and compliance requirements. The role involves training on new tools, including generative AI platforms, and becoming an expert in new content creation skills and technologies.

The Manager of Medical Communications and Content Solutions (MCCS) at Pfizer is responsible for developing a wide range of medical affairs content, including abstracts, manuscripts, presentations, and digital media. This role involves researching, organizing, and interpreting medical information, collaborating with cross-functional teams, and ensuring the accuracy and compliance of all content. The manager will also support the development of training materials and stay updated on trends in medical content generation, including the use of generative AI technologies.

Medical Advisor role at Pfizer focusing on hematology in China. Responsibilities include developing medical strategies, managing local data generation, supporting drug registration, providing medical input to business decisions, training sales forces, and academic communication. The role requires deep therapeutic area knowledge and ensuring medical compliance.

This role is responsible for defining and executing the Candidate Experience (CX) strategy in Japan, ensuring a high-quality and scalable hiring process that aligns with global frameworks while addressing local market dynamics and regulatory requirements. The lead will partner with business leaders, HR, recruiters, and RPO partners to manage the end-to-end candidate journey, build capabilities, influence stakeholders, and drive continuous improvement. Key responsibilities include strategy governance, CX delivery across all hiring segments, stakeholder partnership, data analysis for insights, people leadership, and ensuring compliance with Japanese labor laws. Experience in recruitment, people management, and working in large multinational firms is required, with a preference for experience in matrix organizations or the pharma/healthcare industry. Fluency in Japanese and English is essential.

This role is for an Employee Relations Manager in the HR Planning department at Pfizer Japan. The primary focus is on strengthening organizational capabilities and improving performance through HR initiatives, fostering corporate culture, and enhancing employee engagement. Key responsibilities include planning and implementing HR strategies, managing labor relations and union negotiations, ensuring compliance with labor laws and regulations, overseeing outsourced HR operations, and participating in cross-functional projects. The role requires deep knowledge of labor laws, HR policies, and strong project management and communication skills, with a preference for experience in labor relations or employee relations.

This role is for a Senior QC Chemist at Pfizer in Singapore, focusing on performing analytical method transfer, validation, and verification according to SOPs, GMP, and GLP. Responsibilities include supporting regulatory submissions, conducting investigations, training colleagues, reviewing results, and contributing to continuous improvement. The role requires a Bachelor's degree or equivalent experience and demonstrated technical skills in method validation and testing, with preferred experience in HPLC, GC, and AI tools for productivity.

This role involves collecting, assessing, and managing safety information for Pfizer's marketed and investigational products. Responsibilities include data entry into global safety databases, ensuring compliance with Japanese, US, and European regulations, supporting audits and inspections, responding to queries, and contributing to global safety process development projects. The role requires fluent Japanese, medical or science background, and English communication skills.

Responsible for regulatory activities related to post-approval CMC (Chemistry, Manufacturing and Controls) change management for pharmaceutical products, contributing to the maintenance of a stable and continuous product supply. This includes managing product approval changes, changes for drug manufacturers, and developing regulatory strategies for applications. The role also involves providing regulatory information to Development Japan, and developing and managing internal cross-functional processes.

This role involves monitoring drug surveillance programs, processing adverse reports for clinical trials and post-marketing activities, and ensuring compliance with regulatory requirements and corporate policies. The associate will analyze post-marketing safety data and determine appropriate workflows for case processing.

Project Manager role within Pfizer's Portfolio Project Management (PPM) group in Japan. The role focuses on maximizing product value throughout all stages from introduction to post-market lifecycle management. Responsibilities include leading cross-functional teams, developing and executing development strategies, ensuring alignment between R&D and commercial departments, and managing lifecycle plans for new and existing products. Requires strong leadership, project management experience in the pharmaceutical industry, knowledge of drug development and commercialization processes, and English communication skills.

Responsible for the clinical development of assigned projects in Japan, working under the supervision of the Japan Development Leader. This role involves formulating and executing global and Japan development strategies, evaluating candidates, leading clinical studies, and preparing documentation. Requires strong scientific, leadership, and project management skills, with fluency in both Japanese and English.

Statistician role at Pfizer focused on clinical trial design, analysis, and interpretation, ensuring compliance with regulatory requirements and company standards. The role involves collaborating with clinical development teams, providing statistical expertise, and contributing to drug development plans and regulatory submissions. Requires advanced statistical skills, understanding of drug development, and knowledge of clinical medicine and regulations.

The Medical Content Operation Manager at Pfizer will oversee the entire lifecycle of online medical content for priority therapeutic areas, ensuring high-quality content experiences for healthcare professionals (HCPs) and patients. This role involves close collaboration with various internal teams and external agencies to develop content plans, manage production processes, ensure accuracy and consistency, and explore innovative content models, all while adhering to scientific standards and company SOPs.

Responsible for statistical operations related to clinical trials and regulatory submission documents for vaccine projects. This includes creating and managing the quality of statistical analysis plans, providing statistical advice on development plans and protocols, and supporting programming tasks as needed. The role involves global collaboration and reporting directly to Global Vaccine Research.

The Medical Affairs Scientist (MAS) role at Pfizer Japan serves as a key medical scientific point of contact for healthcare professionals, medical societies, regulators, and academia. This role involves providing and exchanging medical scientific information, contributing to the implementation of local medical strategies, identifying unmet medical needs, and conducting scientific exchanges with healthcare professionals to ensure the safe and efficacious use of products.

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.