Associate Manager - Microbiology

Pfizer; India; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Pfizer India is seeking a qualified QA professional to lead method validation, transfer protocols, and equipment qualification within Quality Control and Stability labs. The role involves maintaining CGMP compliance, supporting microbiology operations, and collaborating on cross-functional teams to uphold safety and data integrity.

Ideal candidates hold an MSc in Microbiology/Biochemistry/Biotechnology with 6–12 years of industry experience, and are skilled in LIMS and quality systems.

Qualifications

• M.Sc. in Microbiology, Biochemistry or Biotechnology with 6–12 years in industry.
• Strong skills in method validation, testing, and sterility assays.
• Experience in QA/Quality Assurance in pharmaceutical manufacturing.
• Knowledge of regulatory requirements and quality systems.
• Excellent communication and collaboration skills.

Responsibilities

• Create, review, and approve test method transfer/validation protocols, reports, and equipment qualification records.
• Maintain CGMP compliance in Quality Control and Stability labs.
• Support media preparation, Bio ball culture handling, and microbiology investigations.
• Perform testing, manage LIMS builds, and review laboratory data.
• Contribute on cross-functional teams, conduct safety inspections, investigations, and train juniors.

Skills

Quality control

GxP compliance

Sterility testing

Microbiology

Lab data analysis

Education

MSc Microbiology

MSc Biochemistry

MSc Biotechnology

Tools

LIMS

Job description

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

• 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, Biochemistry, Biotechnology with 6-12 years of industry experience
• Strong technical skills in method validation and testing NPI Developmental studies, MLT, BET, Sterility, Assay. Heat Shock tests and culture management.
• Experience in microbiological sterility testing
• Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations
• Detail-oriented with robust knowledge of quality systems
• Familiarity with analytical laboratory environments
• 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

辉瑞是平等机会的雇主，并且在其运营的每一个司法管辖区遵守所有适用的平等就业机会立法。

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 职业生涯与众不同。在我们的主人翁文化中，我们相信我们能够让医疗保健行业未来更美好，我们有潜力改善数以百万计人的生活。我们正在寻找新人才，加入我们的全球人才队伍，开发创新疗法，让世界变得更健康。