Pfizer
Pharma · Pharma
- HQ
- New York City, US
- Founded
- 1849
- Size
- 75,000+
- Website
- pfizer.com
Pharma · Pharma
Pfizer has 19 active AI-related job listings. The majority of these roles are focused on agents, accounting for 32% of the openings, followed by data roles at 26%. Engineering is the most frequent function, with 14 positions. The company is actively hiring for roles involving agent orchestration, model serving, and RAG. Over the last 30 days, Pfizer posted 45 new AI roles.
Currently tracking 10 active AI roles, down 57% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $65k–$358k (avg $176k).
Pfizer currently has 18 active AI-related roles in our index. The most common open titles are: Clinical Development Scientist, Director (Inflammation and Immunology) (2), AI Data Engineer--LLMs / Agentic Systems, AI/ML Engineer - Vaccine Research, Business Title Senior Scientist, Sterile Injectables Design, Director of AI Engineering – Vaccine R&D Operations Enablement. Most positions are in Engineering and Product.
Pfizer's active AI hiring is concentrated in: application (44%), agents (28%), post-training (11%). These categories follow a seven-stage AI lifecycle: data, pre-training, post-training, serving infrastructure, agents, evaluation, and application.
Pfizer is hiring AI talent in: United States (13 roles), China (2 roles), Spain (1 role), India (1 role).
Job postings at Pfizer most frequently reference: llm observability, model serving, rag, agent orchestration, fine tuning.
In the past 30 days, Pfizer has posted 24 new AI-related roles. That is a -27% change versus the prior 30 days (33 → 24).
| Title | Stage | AI score |
|---|---|---|
| EHS Senior Associate – Environmental Lead The EHS Senior Associate – Environmental Lead role at Pfizer focuses on supporting and co-leading EHS projects, with a primary emphasis on environmental programs such as waste management, sustainability, and regulatory compliance. The role involves risk assessments, audits, inspections, maintaining EHS management systems, and liaising with legal and regulatory bodies. Responsibilities include developing training, assessing risks, and ensuring compliance with safety and environmental standards within a pharmaceutical manufacturing context. | — | 0 |
| Senior Director, Vaccine Development Management Senior Director role at Pfizer focused on overall project management expertise for Vaccines Global Product Teams, ensuring strategic and operational objectives are met from early development through licensure. Requires extensive experience in vaccine development, project management tools, and cross-disciplinary team leadership within a matrixed organization. | — | 0 |
| Senior Production Operator (SPO) 1 This role is for a Senior Production Operator at Pfizer, focusing on manufacturing support functions in a pharmaceutical setting. Responsibilities include performing light inspections, manual and automated manufacturing support, operating various machinery, ensuring product quality, maintaining documentation, and performing cleaning and sanitation. The role also involves training new colleagues and acting as a backup for the Group Leader. It requires a high school diploma, minimum 6 months of relevant experience, and the ability to perform physical tasks associated with manufacturing. |
| — |
| 0 |
| Program Manager, Vaccine Development Program Manager at Pfizer responsible for overseeing vaccine development projects from research through registration, ensuring alignment of strategic and operational objectives. This role involves project planning, execution, risk management, budget development, and cross-functional team facilitation within the pharmaceutical industry. | — | 0 |
| Director, Veeva Clinical CTMS Lead Director, Veeva Clinical CTMS Lead at Pfizer, responsible for providing leadership and subject matter expertise in drug development processes, change management, and support for Clinical Data & Information Sciences systems. The role focuses on digitizing drug discovery and development, ensuring system data integrity and compliance with regulations, managing critical information, and driving innovation within the organization. Key responsibilities include facilitating system integration, defining strategies, leading continuous improvement programs, and interfacing with business and technical groups to gather requirements and improve processes. The role also involves serving as a subject matter expert for regulators and providing inspection readiness consultation. | — | 0 |
| Associate Scientist-Vaccines Associate Scientist in Vaccines at Pfizer, focusing on conducting immunological assays for vaccine clinical development under GCLP, managing reagent inventory, presenting data, analyzing results, and executing sample testing for toxicology and clinical trials. Requires a BA/BS with 0-2 years of experience, strong attention to detail, teamwork, computer proficiency, and experience in bioassay development and Luminex technology. | — | 0 |
| Senior Director, US Medical Affairs, Obesity, MD Senior Director, US Medical Affairs for obesity drug, focusing on strategy, evidence generation, and external engagement. Requires MD with 5+ years industry experience, preferably in obesity or related therapeutic areas. Role involves budget management, cross-functional coordination, and thought leader engagement. | — | 0 |
| Senior Director, US Medical Affairs, Obesity, non-MD This role provides strategic and scientific leadership for US Medical Affairs activities supporting berobenatide in obesity and obesity-related comorbid conditions. It is accountable for shaping and executing the US medical strategy across the product lifecycle, with a strong emphasis on US medical affairs strategy, evidence generation, cross-functional coordination, and external scientific engagement. | — | 0 |
| Field Medical Director_Oncology STEP (MD) The Field Medical Director (MD) for Oncology at Pfizer is responsible for providing therapeutic area and product expertise, developing and executing medical strategy, engaging with healthcare professionals (HCPs), and serving as a conduit for medical information and customer insights within a designated territory. This role requires deep knowledge of oncology, clinical trial processes, and the ability to communicate complex medical information effectively. | — | 0 |
| Field Medical Director_Oncology STEP (MD) The Field Medical Director for Oncology at Pfizer is responsible for providing therapeutic area and product expertise, executing medical strategy, and engaging with healthcare professionals within a designated territory. This role involves delivering approved medical content, responding to medical inquiries, supporting clinical trial site identification, and cultivating research expertise. The position requires an MD or DO degree and significant experience in a relevant field, with strong communication, collaboration, and leadership skills. | — | 0 |
| Field Medical Director_Oncology STEP (non-MD) The Oncology Field Medical Director is responsible for providing therapeutic area/product expertise for Solid Tumors and Early Pipeline support across various customer segments and initiatives. This role involves planning and executing medical strategy, maintaining knowledge of disease states and medicines, serving as a conduit for medical information and customer insights, and contributing to medical content strategy. | — | 0 |
| Field Medical Director_Oncology STEP (non-MD) Pfizer is seeking a Field Medical Director in Oncology to provide therapeutic area and product expertise, develop and execute medical strategy, and serve as a conduit for medical information and customer insights. The role involves engaging with healthcare professionals, supporting clinical trial identification, and collaborating with internal and external stakeholders. | — | 0 |
| Global Development Lead, Internal Medicine, Sr. Director (non-MD) Pfizer is seeking a Global Development Lead for Internal Medicine, a senior role responsible for the clinical development of assigned assets. This individual will lead cross-functional teams in designing, executing, and interpreting clinical studies, contributing to regulatory submissions, and providing subject matter expertise in their therapeutic area and clinical drug development. The role requires a PhD/PharmD with extensive experience in clinical development, regulatory affairs, and team management. | — | 0 |
| Global Development Lead, Internal Medicine, Sr. Director (MD) Pfizer is seeking a Global Development Lead (GDL) for Internal Medicine, Sr. Director (MD) to lead clinical development for assigned assets. This role involves designing, executing, and interpreting studies, creating clinical development plans, and partnering with cross-functional teams and external stakeholders. The GDL will also contribute to regulatory submissions and product labels, ensuring compliance with internal and external standards. Requires an MD or DO with extensive experience in clinical drug development, regulatory affairs, and team management within the biopharmaceutical industry. | — | 0 |
| Senior Principal Scientist, Pre-Formulation and Materials Science Senior Principal Scientist role in Early Formulation Science and Drug Delivery (EFS-DD) group at Pfizer, focusing on early-stage drug and drug product design, materials science characterization, biopharmaceutics, and drug delivery strategy for new small molecules. The role involves interfacing with multi-disciplinary research teams, providing guidance on molecular design, dosage form design, solid form strategy, and biopharmaceutics for pre-clinical and clinical candidate development. Key activities include understanding molecular interactions, crystallization, polymorph behavior, and applying modeling/simulation tools for predictive performance. The role also emphasizes leading matrix teams, scientific strategy, and conducting novel research. | — | 0 |
| Senior Scientist, Early Formulation Science and Drug Delivery, Drug Product Design This role focuses on early formulation science and drug delivery for small molecule drug candidates at Pfizer. The Senior Scientist will act as a subject matter expert, influencing candidate selection based on drug delivery, bio-performance, and stability. Responsibilities include designing and interpreting experiments (in vitro, in silico, in vivo), developing formulations for preclinical studies, and assessing material science and physicochemical properties. Collaboration with Medicinal Chemistry, Pharmacokinetics & Drug Metabolism, and Clinical Pharmacology is key. The role also involves developing strategic collaborations and conducting novel research, with potential for internal/external presentations or publications. | — | 0 |
| Oncology Clinical Development Scientist, Director Pfizer is seeking a Director of Oncology Clinical Development Scientist to provide scientific oversight, ensure data integrity, and manage the quality of clinical trials for late-stage oncology programs. The role involves authoring protocols, contributing to regulatory documents, setting clinical data review strategies, analyzing safety profiles, and ensuring compliance with SOPs and regulations. Requires extensive experience in clinical research, particularly in oncology phase 3 trials, and leadership experience. | — | 0 |
| Development Head, RSV, RSV Combination, and Early Vaccine Programs This role is for a Development Head overseeing vaccine clinical research and development programs at Pfizer. The position requires extensive expertise in clinical research, program design, and regulatory activities to ensure successful implementation and registration of vaccine candidates. Responsibilities include leading global clinical research programs, providing scientific and procedural expertise, managing clinical project teams, and ensuring quality and safety across studies. The role also involves potential in-licensing reviews and contributing to business development. A medical degree and over 10 years of pharmaceutical industry experience in clinical research are required, with specific experience in end-to-end vaccine clinical development. | — | 0 |
| Senior Medical Director, Hematology Senior Medical Director in Hematology responsible for supporting clinical trials, leading subteams in clinical development, and contributing to development strategies and regulatory interactions within the pharmaceutical industry. | — | 0 |
| Sr. Packaging Engineer This role focuses on the selection, qualification, and implementation of packaging components and container closure systems for pharmaceutical products, including combination products. It involves supporting formulation and process development, authoring technical documentation, participating in design control teams, conducting investigations, driving testing activities, and authoring regulatory submission content. The role requires strong technical expertise in parenteral packaging, medical device development, and regulatory compliance within a cGMP environment. | — | 0 |
| VP, Global Head of Statistics VCRD Seeking a VP, Global Head of Statistics for Vaccine Clinical Research and Development (VCRD) to set vision and provide leadership for data management, modeling, and statistical advice across a complex portfolio of clinical development projects. This role requires deep expertise in statistical analysis tools, regulatory guidelines (FDA, ICH), and managing a large team of statisticians and modelers. | — | 0 |
| Robotics & Automation Technical Associate (Associate's degree) Associate's degree level role focused on operating, maintaining, and calibrating laboratory and robotic equipment in a regulated GxP setting for Pfizer's Vaccines division. Responsibilities include performing routine maintenance, documenting work in LIMS/ELN, and ensuring compliance with standard operating procedures. | — | 0 |
| Principal Packaging Engineer- Drug Product Design & Development This role is for a Principal Packaging Engineer in Biotherapeutics Pharmaceutical Research & Development at Pfizer. The individual will lead a team, provide strategic direction for laboratory operations supporting drug product and combination product development, and champion quality and compliance. Responsibilities include overseeing testing activities, component and container closure system selection, and authoring regulatory submission content. The role requires strong expertise in parenteral packaging, medical device/combination product development, and experience in GMP/ISO 13485 environments. | — | 0 |
| Oncology Clinical Development Scientists (Senior Manager) This role is for a Senior Manager in Oncology Clinical Development at Pfizer, responsible for scientific oversight, data integrity, and quality of clinical trials. The position involves authoring protocols, reviewing clinical data, analyzing safety profiles, and ensuring compliance with regulations and SOPs. It requires a strong background in clinical research within the oncology space, experience with large datasets, and collaboration with cross-functional teams. | — | 0 |
| Clinical Development Medical Director, Hematology Medical Director providing Clinical Development leadership for late-phase Hematology clinical trials, overseeing design, conduct, and analysis. Collaborates with cross-functional teams (regulatory, pharmacovigilance, biostatistics, medical affairs) and external stakeholders to ensure scientific, ethical, and regulatory standards are met. Responsibilities include medical monitoring, data review, safety monitoring, investigator interactions, and contributing to clinical and regulatory documents. Provides strategic guidance and interprets clinical data. | — | 0 |
| Director, Oncology AI Product & Engineering Lead | — | — |
| Senior Manager, AI, and Data Engineering | — | — |
| Senior Manager, Scientific AI Engineer | — | — |
| Prostate Field Medical Director (non-MD) | — | — |