Similar Jobs at Pfizer
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Leads terminal sterilization manufacturing operations, managing process technicians, equipment, facilities, projects, resources, and team performance. Ensures compliance with SOPs, cGMP, and regulatory requirements while driving process improvements, Lean implementation, equipment qualification, training, and best-practice sharing. Partners with leadership, develops SMART objectives, solves complex operational problems, and supports performance management for employees and contingent staff.
Top Skills:
CgmpChatgptLean ToolsMicrosoft Copilot
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Investigates pharmaceutical manufacturing and laboratory quality issues, including deviations, out-of-specification results, and atypical findings. Identifies root causes, recommends corrective actions, and ensures investigation reports meet regulatory and company requirements. The role supports moderately complex projects, manages work independently, collaborates with teams, resolves routine problems, and may mentor colleagues. Strong knowledge of pharmaceutical manufacturing, compliance, technology investigations, quality systems, communication, problem-solving, and Excel is required.
Top Skills:
ChatgptExcelMicrosoft Copilot
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Manage pharmaceutical quality system documentation and records, including issuance, retrieval, archival, retention, disposition, scanning, metadata verification, audit trail review, and record tracking. Support document lifecycle management, records retention compliance, logbook and storage administration, change control, impact assessments, and quality systems processes. Collaborate across functions and use digital and AI tools to improve workflows. Shift-based work may be required.
Top Skills:
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Leads microbiology quality control activities, including method transfer and validation, equipment qualification, cGMP compliance, sterility and assay testing, investigations, LIMS builds, data review, corrective actions, safety inspections, and training. The role requires pharmaceutical microbiology expertise, bio-assays, method development, pharmacopeial methods, reagent management, and cross-functional collaboration.
Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy.
What You Will Achieve
In this role, you will:
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements)
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy.
What You Will Achieve
In this role, you will:
- Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records.
- Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories.
- Support media preparation, Bio ball culture handling, and conduct microbiology-related investigations.
- Perform testing on various samples, manage Laboratory Information Management System builds, and review laboratory data.
- Serve on cross-functional teams, conduct safety inspections, participate in investigations, recommend corrective actions, and train junior colleagues.
Here Is What You Need (Minimum Requirements)
- M.Sc. Microbiology or related masters with 8+ years of industry experience
- Strong technical skills in method validation and testing
- NPI MLT, BET, Sterility, Assay.
- Bio-Assay expertise
- Method development for new products
- Experience in microbiological sterility testing
- Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations
- Detail-oriented with robust knowledge of Reagents management
- Familiarity with pharmacopeia methods and developments
- Effective written and verbal communication, as well as interpersonal skills
Bonus Points If You Have (Preferred Requirements)
- Relevant pharmaceutical experience
- Strong understanding of computer system hardware, infrastructure, and networks
- Experience with Laboratory Information Management Systems (LIMS)
- Proficiency in data analysis and interpretation
- Knowledge of regulatory requirements and guidelines
- Strong problem-solving abilities
- Effective time management and organizational skills
- Ability to mentor and train junior colleagues
- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
Pfizer Chennai, Tamil Nadu, IND Office
Chennai, India
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