Pfizer

Seeking a Postdoctoral Fellow to develop AI/ML enabled bioprocess models and control strategies for recombinant protein production. The role involves creating hybrid mechanistic-data driven models, integrating omics data, applying ML/DL for prediction, and exploring agentic AI for model orchestration and transfer learning. Responsibilities include designing experiments, implementing model predictive control, validating models, and communicating results.

This role leads the strategy and technical direction for applied AI in Inflammation & Immunology at Pfizer, focusing on translating advances in LLMs, agentic systems, and multimodal AI into reusable capabilities. The position involves shaping the AI portfolio, defining governance and evaluation standards, managing external partnerships, and driving AI adoption across scientific decision-making processes. It requires a technically credible leader with strong scientific judgment to ensure solutions are robust, trusted, and improve the speed and quality of evidence generation.

Senior Manager role focused on designing, developing, and deploying AI agents for enterprise workflow automation, decision enhancement, and intelligent user interactions. Requires experience with agentic orchestration frameworks, vector databases, RAG, and LLM principles, along with leadership in managing technical teams and delivering enterprise-scale projects.

AI/ML Engineer role focused on vaccine research, applying AI/ML to discover and develop vaccines. Responsibilities include shaping scientific strategy with AI, owning foundational and predictive modeling end-to-end, advancing generative AI for vaccine design, engineering robust ML systems, decoding high-dimensional biology, and elevating AI fluency. Requires PhD or Master's with experience in AI/ML within life sciences, knowledge of vaccine R&D, and expertise in foundation models, generative AI, and ML system design.

This role focuses on building and deploying production-grade full-stack applications that integrate LLM and AI capabilities into pharmaceutical research workflows. Responsibilities include developing backend services for data processing, embedding generation, vector search, and LLM orchestration, creating frontend interfaces, implementing RAG systems and agentic LLM architectures, and deploying/maintaining systems on AWS. The role also involves contributing to semantic frameworks and conceptual research.

Senior Manager, Applied AI Workflow Scientist at Pfizer, focused on applying LLMs and agentic AI to scientific use cases in Inflammation & Immunology. The role involves identifying high-value scientific applications, building reusable AI workflows and agentic systems, and partnering with scientists to ensure adoption and impact. It emphasizes practical application, scientific credibility, user partnership, and scalable workflows.

Director of AI Engineering role focused on applying AI automation and advanced analytics in regulated healthcare R&D operations. The role involves leading the definition and delivery of AI solutions for lab and office workflows, strengthening operational decision-making through predictive models, enabling regulated AI systems with governance, optimizing development planning, and engineering/scaling production-grade ML platforms. Requires expertise in predictive modeling, optimization, automation, generative AI, and ML system design, with strong programming skills in Python and ML frameworks, and experience scaling models in cloud/HPC environments. Collaboration across scientific, operational, quality, and business teams is critical.

Senior Director, US Commercial Product Lead, AIA at Pfizer. Owns the AI product roadmap for US Commercial, ensuring strategic alignment and delivery of AI-driven solutions. Leads a team of Product Owners, manages a budget, and collaborates with Commercial, Digital, and Analytics teams. Ensures adherence to data privacy, security, and ethical AI standards. Drives stakeholder engagement and change management for AI capabilities adoption. Accountable for delivering measurable business outcomes through AI.

This role is primarily focused on medical information and review within the healthcare domain, ensuring scientific accuracy and compliance of promotional and non-promotional content. While the role requires demonstrating AI fluency and using approved AI tools, its core function is not the development or direct application of AI/ML models, but rather the application of AI tools to enhance existing processes in medical information and review.

Product leader responsible for owning and delivering AI capabilities for content creation, review, and approval processes within Pfizer's commercial marketing organization. This role involves defining and executing a product roadmap, driving stakeholder engagement, and partnering with cross-functional teams to deliver AI-enabled solutions.

Internship role supporting data analytics, business intelligence, and AI-enabled initiatives within Pfizer's Commercial Excellence & Innovation team. Focuses on improving data quality, translating data into insights, and supporting early AI/advanced analytics use cases in a regulated environment. Involves data preparation, analysis using Python/SQL, and exposure to ML concepts, LLMs, and AI agents.

This role is for a Senior Director/Team Head in Oncology Late Stage Data Review at Pfizer. The primary responsibility is to oversee data integrity, analysis, quality, and the adoption of AI and best practices for the Late-Stage Oncology portfolio. The role involves managing and mentoring a team, partnering with various functional lines, setting data review strategies, and ensuring compliance with SOPs and regulations. A key aspect is the application of AI in streamlining data review activities and embracing evolving technologies.

AI Data Engineer focused on Computational Toxicology at Pfizer. The role involves applying Data Engineering and MLOps best practices to automate scientific workflows, curate AI-ready datasets, and enable scalable AI solutions for drug safety science. This includes preparing, structuring, and validating data for AI-enabled toxicology assessments, integrating multi-modal datasets, and implementing scalable data pipelines.

This role is for a Senior Manager, AI and Data Science Solution Engineer at Pfizer in Greece. The primary focus is on implementing technology solutions across various functions, coordinating with delivery engineers, acting as a technical interface, developing user stories, and assisting with test execution. While the role involves using AI tools and understanding responsible AI practices, it does not involve core AI/ML model development or research.

This is a 15-month training program for mid-career professionals in biopharmaceutical manufacturing. The trainee will support the development, implementation, and improvement of industrial automation and digital solutions, including AI-enabled systems, under supervision. The role focuses on building a foundation in automation, digital technologies, and the responsible use of Generative AI within regulated frameworks.

Senior AI Product Manager at Pfizer, focused on developing and launching AI/LLM-driven digital products using rapid prototyping and MVP-first approaches. The role emphasizes defining product vision, collaborating with cross-functional teams, managing lean roadmaps, and driving agile ceremonies to accelerate time-to-value in a fast-paced, experimental environment.

This role is for a senior software engineer who will design, build, and maintain software systems, leveraging AI tools to enhance productivity and verifying AI-generated code. The role involves being embedded with business units (Commercial, Manufacturing, R&D) to act as a 'startup CTO', bridging product building and business problem-solving. Responsibilities include driving technical initiatives, developing technical leaders, shaping technology-driven business strategy, designing AI-augmented engineering workflows, establishing reliability and documentation standards, and driving process efficiency. The role emphasizes curiosity, outcome ownership, polymath orientation, precision communication, and systems thinking, with expert-level skills in business immersion, data integration, full-stack development, multi-audience communication, problem discovery, rapid prototyping, stakeholder management, and team collaboration. Practitioner-level skills include AI evaluation and verification.

This internship within Pfizer's Global Commercial Analytics & AI (GCA) division focuses on supporting the Integrated Insights & Strategy (IIS) team in France. The role involves contributing to performance measurement, investment analysis, and leveraging insights to guide brand strategies. Key responsibilities include market analysis, customer segmentation, advanced analytics support (predictive modeling, data science, machine learning), performance tracking, competitive landscape analysis, forecasting, and managing market research studies. The role emphasizes data-driven decision-making and collaboration with various internal teams.

This role focuses on designing, prototyping, and developing laboratory automation solutions for process development in healthcare, leveraging technologies like computer vision and machine learning. It involves integrating automated hardware, implementing robotic control and data management systems, and using coding languages like Python or C++ for AI/ML applications. The goal is to enhance automation for laboratory experimentation and drug development workflows.

This role focuses on epidemiological research within healthcare, specifically for drug safety surveillance. It involves conducting literature reviews, designing database studies to assess risks and effectiveness of interventions, and engaging with regulatory agencies. While the role mentions using AI tools like ChatGPT, AI/ML is not the core craft.

This role focuses on implementing and overseeing the GCP Quality Management System (QMS) for clinical development activities in China. It involves ensuring compliance with global standards and regulatory requirements, managing inspections and audits, and providing vendor quality oversight. A key aspect is contributing to digital and AI initiatives, supporting AI-enabled processes like Site Start-Up, participant recruitment, eSource, and data analysis, with the goal of improving quality and operational efficiency in clinical development.

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.

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.