Pfizer

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.

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.

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.

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.

This role focuses on managing the operational and regulatory aspects of clinical trial site activation and conduct at Pfizer. It involves coordinating essential documents, ensuring compliance with Good Clinical Practices (GCP) and local regulations, and managing communication between Pfizer, ethics committees, and investigator sites. The role requires a strong understanding of regulatory processes and documentation throughout the study lifecycle.

This role is responsible for ensuring the completeness, quality, and integrity of clinical trial data under a Risk-Based Monitoring (RBM) model. Key activities include developing and implementing RBM systems, defining and monitoring Key Risk Indicators (KRIs), processing and reviewing study data for signal and action management, and ensuring compliance with regulations and SOPs. The role requires technical expertise in clinical trial databases, data management processes, and system setup, as well as strong communication and project management skills.

This role orchestrates global restructuring activities for Colleague Services, integrating with various departments like HR, Finance, and M&A. It involves managing sensitive workforce data, ensuring compliance with labor laws and data privacy, and providing cost analysis and strategic workforce insights to support leadership decision-making. The role requires strong analytical skills, stakeholder management, and the ability to handle confidential information in a fast-paced environment.

Pfizer is seeking an Oncology Field Medical Director with expertise in Malignant Hematology to provide therapeutic area and product knowledge to healthcare professionals within an assigned territory. The role involves planning and executing medical strategy, serving as a conduit for medical information and customer insights, and collaborating with internal teams on clinical trial identification and support. The position requires an MD or DO degree and significant relevant experience, with a strong emphasis on communication, collaboration, and leadership skills in a remote and evolving healthcare environment.

The Medical Review Excellence Manager will partner with in-country Medical Affairs and Marketing teams to review and approve promotional, non-promotional, and internal training materials, ensuring compliance with country laws, regulations, and industry codes. This role involves acting as a subject matter expert, driving continuous improvement in medical review processes, managing stakeholder relationships, and providing consultation for compliant content creation.

Administrative Lead role at Pfizer supporting Vaccine R&D, responsible for day-to-day administrative and business support, calendar management, travel arrangements, meeting organization, procurement, document formatting, training on administrative procedures, and managing onboarding/offboarding logistics. Requires strong organizational, communication, and computer skills, with a minimum of 6 years of administrative experience.

Senior Manager, Data Protection Engineering role at Pfizer, focusing on leading and evolving data protection capabilities. Responsibilities include defining strategy, architecture, and control frameworks for DLP, data discovery, classification, and encryption. The role involves overseeing implementation of data protection technologies, ensuring security-by-design, supporting incident response, and collaborating with Privacy, Legal, and Compliance teams to meet regulatory requirements like GDPR, HIPAA, SOX, and GxP. Requires strong experience in cybersecurity, data protection controls, DLP, data classification, encryption, and cloud integration within regulated environments.

The Oncology Field Medical, Director is responsible for providing therapeutic area/product expertise, including hematology and pipeline, across a broad range of medical customer segments and initiatives in an assigned territory. This role involves planning and executing medical strategy, maintaining knowledge of diseases and medicines, serving as a conduit for medical information and customer insights, and collaborating with internal and external stakeholders. Key responsibilities include delivering approved medical content, identifying and engaging priority customer segments, providing information in response to unsolicited medical requests, supporting clinical trial site identification, and cultivating research and therapeutic area expertise.

This role focuses on developing and executing Health Technology Assessment (HTA), Value & Evidence (HV&E) strategies for Pfizer's early-stage oncology pipeline. The goal is to ensure patients have affordable and timely access to medicines by demonstrating their value to healthcare decision-makers. Responsibilities include developing evidence generation strategies, coordinating with regional teams, creating global value dossiers, conducting HEOR studies, and partnering with external experts.

Pfizer is seeking a Specialty Care & Internal Medicine Medical Lead for the MISP cluster (Malaysia, Indonesia, Singapore, Philippines) to provide medical leadership, develop and execute strategy, and manage the medical team. The role involves cross-functional collaboration with commercial, regulatory, safety, and legal teams, providing medical guidance for product maintenance and defense, and developing strategic partnerships with stakeholders. The lead will also initiate and manage pilot projects for launch excellence and regional medical initiatives, oversee the therapy area medical budget and headcount, and ensure medical quality and compliance. Requires over 7 years of medical affairs experience in pharmaceuticals, with expertise in regulatory/safety risk management, understanding of local health environments and codes of practice, and knowledge of pharmacovigilance and regulatory legislation. An MD is required, with other advanced clinical degrees or an MBA being a plus. Fluency in English is necessary, and local language fluency is preferred. Strong analytical, organizational, communication, and leadership skills are essential, along with the ability to travel within the cluster.

Senior Manager for Pfizer Patient Services, responsible for managing Patient Assistance Programs (PAPs) across various business units. This role ensures programs are developed, maintained, and scaled according to enterprise standards and compliance requirements, collaborating cross-functionally to drive efficiency and consistency. Key responsibilities include managing PAP operations, vendor performance, ensuring compliance with regulations and internal SOPs, troubleshooting operational issues, and modernizing digital engagement experiences. The role also involves data integrity, reporting, and communication with stakeholders.

This role at Pfizer Japan focuses on being a medical scientific point of contact for healthcare professionals and external stakeholders in the Lung Cancer MAS team. The primary responsibilities include demonstrating medical and scientific leadership, developing and executing medical plans to address unmet medical needs, collaborating with medical stakeholders, and contributing to clinical development by providing medical and scientific input.

Clinical Research Manager for Oncology in Japan, responsible for clinical development strategy, execution, and regulatory submissions under the supervision of the Japan Development Leader. Collaborates with global teams, KOLs, and internal stakeholders to advance drug projects.

The role focuses on developing and leading complex projects related to market access strategies, integrating pricing, reimbursement, health technology assessment, and health economic modeling. The Senior Manager will manage economic research studies for clinical trials, formulate research plans, implement analytic strategies, and collaborate with sales teams to assess opportunities using health economic models. The position requires experience in evaluating COA instruments, performing observational research, and understanding global drug development and regulatory standards.

This role leads enterprise offensive security capabilities, including penetration testing, red teaming, and adversary simulation, to identify and prioritize security weaknesses in a highly regulated pharmaceutical environment. It involves partnering with detection and remediation teams to reduce risk and improve defensive outcomes.

Senior Utilities Technician role at Pfizer in Itapevi, SP, Brazil. Responsibilities include diagnosing and repairing equipment issues, performing scheduled preventive electrical maintenance, managing corrective maintenance backlog, identifying and implementing equipment improvements, verifying work results, managing spare parts procurement, and performing low and medium voltage electrical maintenance. The role also involves applying RFT concepts, teamwork, and adhering to Pfizer's manufacturing vision, mission, values, and safety standards. Requires a Technical degree in Electrical Engineering or equivalent, intermediate Excel, Word, PowerPoint, and technical English, with 5 years of prior experience, preferably in the pharmaceutical industry.

Director, Clinical Program Lead at Pfizer in Shanghai, China. This role focuses on leading the clinical development strategy and execution for oncology programs, ensuring adherence to scientific and quality standards, managing timelines, identifying and mitigating risks, and collaborating with internal and external stakeholders. The position requires a strong understanding of clinical trial design, execution, and regulatory requirements within the pharmaceutical industry, with a focus on delivering high-quality clinical deliverables for regulatory submissions and publications. The role also involves people management and ensuring compliance with global and local regulations.

This role at Pfizer focuses on pharmaceutical manufacturing operations, ensuring compliance with cGMP, managing production schedules, supervising operators, and coordinating with other departments for efficient and quality-driven production of medicines. It requires a B Pharmacy degree and experience in manufacturing processes, particularly tablet manufacturing and packaging.

This role supports marketing teams in the compliant execution of commercial activities and events by coordinating activity approvals, managing event administration, and ensuring adherence to Pfizer's ethical, regulatory, and compliance standards. It involves working with cross-functional stakeholders, internal workflow systems, and vendors to manage processes from initiation to closure.

Manager role at Pfizer overseeing clinical studies, focusing on project management, timelines, budget, and ensuring studies meet scope and quality parameters. Requires experience in pharmaceutical R&D and regulatory inspections.

This role at Pfizer focuses on clinical research and development within the healthcare domain. The Sr. Clinician will co-chair clinical study teams, provide clinical and scientific expertise for protocol development, and ensure efficient clinical trial design. Responsibilities include writing protocols, managing study risks, overseeing data quality, selecting sites and investigators, and ensuring regulatory compliance. The role also involves site liaison activities to support trial conduct and maintain relationships with site staff. It requires a deep understanding of disease areas and indications, and may involve mentoring less experienced clinicians.

This role is responsible for performing method transfers, validations, and verifications of complex analytical techniques within a quality control setting at Pfizer. The Associate will interpret and evaluate data for accuracy, ensure compliance with cGMP and GLP, review and revise SOPs, and conduct analyses on finished products, raw materials, and components. The role requires a Bachelor's or Master's degree in Chemistry or Microbiology with relevant experience in analytical testing and a strong understanding of various analytical techniques and regulatory standards.

Associate Manager for Quality Control at Pfizer in India, focusing on ensuring product quality and compliance with GMP in laboratories. Responsibilities include test method validation, media preparation, sample testing, data review, and participation in cross-functional teams. Requires a Master's degree in Chemistry/Microbiology with 5-7 years of analytical testing experience, strong technical skills in method validation, and knowledge of pharmaceutical quality systems. Familiarity with AI tools is a plus.

Internship role focused on supporting and developing features for a web project, involving data cleansing, implementing visualizations, and automating processes. Requires current enrollment in a computer science or related bachelor's degree program and coding experience in JavaScript, Python, or TypeScript.

Operations Administrator at Pfizer in Singapore, responsible for providing administrative and project management support to marketing and medical teams. This includes managing projects, KOL communication, vendor relations, budget oversight, financial processes, and ensuring compliance with company policies and regulations. The role also involves secretarial duties such as travel arrangements, calendar management, and report preparation.

Pfizer is seeking a Quality Assurance Associate in Vizag, India, to ensure the quality, safety, and efficacy of drug products. The role involves reviewing clinical and commercial drug batches, ensuring documentation meets specifications, identifying deviations, approving investigations, and overseeing change control. The associate will contribute to project tasks, maintain compliance with cGMP standards, and support regulatory inspections. This position requires a Bachelor's or Master's degree in Sciences/Pharmacy with relevant experience in the pharmaceutical industry and quality systems.

Senior Process Engineer role at Pfizer focused on leading product manufacturing campaigns, developing and modifying process formulations, methods, and controls to meet quality standards. Responsibilities include technical supervision, process improvements, troubleshooting, ensuring safety and GMP compliance, and collaborating with cross-functional teams in a pharmaceutical manufacturing environment.

This role is for a Senior Process Technician at Pfizer's manufacturing site expansion in Singapore. The technician will operate chemical/fermentation process equipment, perform quality control, handle hazardous materials, and ensure adherence to GMP/GDP standards. Responsibilities include monitoring processes, troubleshooting deviations, documentation, and participating in investigations and commissioning activities. The role requires a technical diploma or GCE 'O/A' levels, 3-5 years of relevant industry experience, and the ability to act decisively and independently.

Senior Associate Quality Assurance role at Pfizer focused on ensuring the quality and compliance of clinical and commercial drug batches. Responsibilities include reviewing batches, conducting statistical process control, approving investigations and change controls, managing projects, and ensuring adherence to GxP and cGMP standards.

This role at Pfizer focuses on Quality Systems, specifically document management and control within a regulated healthcare environment. While the role mentions using AI tools like ChatGPT for productivity, the core responsibilities do not involve building or directly deploying AI/ML models. The primary focus is on ensuring compliance with GMP, GLP, and GCP standards, managing documentation lifecycles, and supporting quality assurance functions.

Pfizer is seeking an EHS Lead for their Melbourne site to oversee environment, health, and safety strategy, ensuring compliance with global and regulatory standards, embedding a strong safety culture, and driving continuous improvement. The role involves managing EHS systems, leading audits, overseeing frontline activities, managing health services, business continuity, and environmental stewardship.

Associate Manager for Manufacturing Quality Assurance (MQA) Downstream operations at Pfizer, focusing on Terminal Sterilization, Visual Inspection, and Packing areas. Responsibilities include ensuring cGMP compliance, reviewing batch records, performing quality checks, and assessing equipment for product quality and patient safety.

This is a 15-month training program for Analytical Chemists in biopharmaceutical manufacturing. The role involves performing chemical analysis using various instruments, compiling and analyzing data, providing manufacturing support, working with vendors, and adhering to good laboratory practices and safety procedures. It is designed for fresh graduates or mid-career individuals with no prior experience in the biopharmaceutical sector.

Manager for Quality Assurance Batch Release in a pharmaceutical manufacturing facility, ensuring compliance with cGMP and overseeing daily release activities, exception reports, and team performance. Requires extensive experience in pharmaceutical quality systems and people management.

The People Experience Manager partners with the Commercial Leadership Team to translate business priorities into effective people strategies, focusing on building colleague capability, talent readiness, organizational effectiveness, compliance, employee relations, and a high-performance culture. This role requires integrity, structure, influence, and disciplined execution in a complex, matrixed environment.

This is a 15-month training program for fresh or mid-career individuals to enter the biopharmaceutical manufacturing sector at Pfizer in Singapore. The role involves laboratory-scale experiments, process development, troubleshooting, and collaboration with various functions to ensure product quality and continuous improvement.

This is a QA Specialist role focused on compliance within pharmaceutical manufacturing. The role ensures adherence to Good Manufacturing Practices (GMP), Pfizer Quality Standards, and regulatory guidelines. Responsibilities include quality oversight of vendor management, managing inspections, collaborating with cross-functional teams, and maintaining quality systems. The position is part of a training program for advanced biopharmaceutical manufacturing professionals.

Internship position focused on pharmaceutical marketing assignments to increase engagement with Health Care Professionals (HCPs) in Singapore. Responsibilities include supporting marketing functions, managing time and professional development, and identifying process improvement activities. Requires active enrollment in an undergraduate program, data interpretation skills, strong organizational and communication skills, and proficiency in Microsoft Office.

Pfizer is seeking an Associate Manager for Process Engineering in Vizag, India. This role is responsible for the design, implementation, optimization, and validation of manufacturing processes and facilities, adhering to cGMP, regulatory, and safety standards. Key responsibilities include process automation, technology transfer, CIP/SIP design, equipment and facility engineering, continuous improvement, new facility design, CQV activities, and DCS & Automation recipe development. The ideal candidate will have a B.Tech/M.Tech with at least 6 years of experience in the pharmaceutical industry, including greenfield/brownfield projects and experience in MSAT/R&D/Process Engineering. Experience with DCS systems like DeltaV and AI tools is preferred.