Pfizer

Reliability Engineer at Pfizer in Australia, focusing on maintenance and reliability of utility systems, buildings, and equipment within the pharmaceutical industry. The role involves project support, operational support, Root Cause Failure Analysis, and ensuring GxP compliance. Experience with AI tools is a bonus.

Equipment Engineer responsible for the maintenance, repair, and installation of all equipment, general engineering, and infrastructure at the Wuxi factory. This includes participating in annual overhauls, developing maintenance plans, managing spare parts, ensuring GMP compliance, and documenting procedures.

Recruiting role at Pfizer focused on developing and implementing recruitment strategies, sourcing candidates, managing the recruitment cycle, and leveraging employer branding to attract and retain talent. Requires experience in full-cycle recruitment, talent sourcing, stakeholder management, and data analysis, with preferred experience in the pharmaceutical industry.

This role is for a Global Workplace Experience (GWE) Manager at Pfizer, responsible for delivering Real Estate and Facility Management Services and leading workplace transformations in Hong Kong, Macau, Taiwan, and South China. The manager will oversee real estate properties, facilities operations through outsourcing partners, ensure compliance with EHS and Global Security standards, manage vendors, develop business continuity plans, and lead sustainability initiatives. The role requires a minimum of 3 years of direct RE&FM experience in multinational companies, preferably in the pharmaceutical industry, with strong written and spoken Chinese and English skills. Experience in managing outsource deals and project management knowledge is desirable. Technical competencies include Real Estate Strategic Management, Engineering/Construction/Architectural skills, Construction Support and Project Planning, EHS understanding, Analytical Skills, Contract Management, and Capital Planning. Behavioral competencies include strong Communications, Networking, and Analytical Thinking.

Operates and maintains pharmaceutical manufacturing equipment, ensuring production tasks are completed safely, on time, and with quality, adhering to company and regulatory standards (GMP, PQS, EHS). Responsibilities include following SOPs, maintaining equipment, ensuring site hygiene, participating in new product/equipment trials, and assisting with training and validation. Requires vocational or associate degree with relevant experience in pharmaceutical manufacturing and knowledge of GMP and other regulations.

Operate manufacturing equipment and manage materials to produce pharmaceutical products, ensuring adherence to safety and cGMP regulations. This role involves problem-solving, quality inspections, and process improvement within a manufacturing environment.

This role is for a Pharmaceutical Manufacturing Operator I at Pfizer in Wuxi, China. The primary responsibilities involve executing manufacturing tasks according to established procedures, ensuring compliance with cGMPs, troubleshooting issues, and contributing to team deliverables. The role requires a high school diploma, 4+ years of experience in pharmaceutical manufacturing, and strong communication and organizational skills. While not AI-related, it mentions familiarity with common AI tools as a bonus.

Operate manufacturing equipment and manage materials to produce pharmaceutical products, ensuring adherence to safety and cGMP regulations. This role involves problem-solving, quality inspections, and process improvement within a manufacturing environment.

Manager for Equipment Technology, specializing in Filling Line SME at Pfizer's Vizag location. This role focuses on the design, development, maintenance, and reliability of manufacturing processes and equipment, particularly IMA filling lines, to ensure efficient and reliable production of medicines. Responsibilities include technical support, performance optimization, project management, cross-functional leadership, and ensuring compliance with cGMP and regulatory standards.

Occupational Health Nurse at a pharmaceutical factory's Wellness Center in Japan, responsible for emergency response, health check-ups, stress checks, health guidance, mental health support, workplace environment management, health education, and collaboration with EHS and management.

Senior QC Laboratory Analyst at Pfizer in Singapore, responsible for supporting the Reference Standards Program. Duties include meeting KPIs, certifying reference standards, adhering to safety and cGMP policies, conducting analytical testing, equipment training and maintenance, troubleshooting, managing lab inventories, reporting deviations, participating in investigations and audits, and guiding junior analysts.

The Associate Manager for MSAT (Manufacturing Science and Technology) in C&Q (Commissioning & Qualification) at Pfizer's Vizag facility is responsible for overseeing and executing validation processes for pharmaceutical manufacturing. This includes evaluating and approving validation documentation, troubleshooting issues, conducting statistical analysis, managing quality systems, and ensuring compliance with Good Manufacturing Practices and regulatory requirements. The role also involves supporting product transfers, new product development, and continuous improvement projects within a regulated healthcare environment.

This role is for a Process Safety Engineer within Pfizer's Career Progression Program, focusing on ensuring compliance with environmental, health, and safety regulations in biopharmaceutical manufacturing. The program offers 15 months of training and aims to develop professionals for the biopharmaceutical sector. Responsibilities include assisting with facility modifications, managing waste disposal contracts, monitoring waste handling, and updating safety procedures. The role requires a Bachelor's degree and experience in industrial safety, with preferred knowledge of risk assessment and AI tools for productivity enhancement.

Pfizer is offering a 15-month Career Progression Program (CCP) for advanced biopharmaceutical manufacturing executives/professionals in Singapore. The program is designed to cultivate skilled professionals for the biopharmaceutical manufacturing sector, targeting fresh graduates and mid-career individuals with no prior experience in the field. Participants will gain essential skills and experience in developing and modifying manufacturing processes, troubleshooting control systems, ensuring quality and safety standards, and implementing process improvements. The role requires a degree in Engineering (preferably Chemical) or Science (Chemistry major) and strong interpersonal and communication skills.

This role is for a QC Chemist within Pfizer's biopharmaceutical manufacturing sector, focusing on performing and documenting analytical testing, troubleshooting lab issues, and authoring GMP documentation. It is part of a training program for advanced biopharmaceutical manufacturing professionals.

Seeking a China Cloud Engineer to manage cloud hosting services (AWS China, Azure China), servers, storage, networks, and operating systems in China. The role requires hands-on implementation skills, ensuring infrastructure solutions align with global engineering standards and comply with China's PIPL and related regulations. Responsibilities include infrastructure deployment, automation, security, and collaboration with global and local teams.

Pfizer is seeking a China Platform Engineer to manage platform technologies including databases and mid-tier services in Dalian, China. The role involves ensuring platform deployments comply with China's PIPL and global engineering standards, collaborating with global and local teams, and driving continuous improvement in automation and performance.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Supervisor de Producción at Pfizer in Buenos Aires, Argentina. This role involves supervising and coordinating production operations, ensuring compliance with Quality, GMP, EHS, and Data Integrity standards. Responsibilities include leading operational teams, managing the production plan, analyzing deviations, driving continuous improvement initiatives, and collaborating with internal departments. Requires a university degree, 3-5 years of experience in the pharmaceutical industry, and knowledge of GMP in regulated environments.

Pfizer is seeking a Director of Cloud Engineering to lead their multicloud strategy and engineering organization. This role is responsible for driving cloud modernization, platform reliability, and engineering innovation on a global scale, supporting the company's mission to deliver breakthroughs that change patients' lives. The director will shape cloud architecture, evolve engineering practices, and ensure cloud platforms are secure, compliant, scalable, and efficient, leading multiple teams of cloud engineers and fostering a culture of innovation and excellence.

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