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 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.

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.

This role is for an Assistant Associate in Engineering Stores at Pfizer, responsible for managing material receipts, storage, and issuance within the manufacturing logistics and supply team. The position involves using systems like SAP MM/EAMS/ARIBA, adhering to cGMP and safety procedures, and ensuring efficient material flow to support patient access to medicines. Key duties include inventory management, documentation, and supporting audits.

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 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 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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.