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Salary
≈ $18k – $40k per year (Estimated)
Location
In office (India)
Seniority
Junior · 6+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 12, 2026. First seen by Alion on Oct 10, 2026.

Overview
Company
Impact
Profile match
Pfizer is an American multinational pharmaceutical and biotechnology company headquartered in New York City, developing, manufacturing and marketing prescription medicines and vaccines in areas such as oncology, internal medicine, inflammation and immunology, and infectious diseases. Founded in 1849 by Charles Pfizer and Charles Erhart, it is listed on the New York Stock Exchange and operates research and manufacturing sites across the US, Europe and Asia, including a digital hub in Thessaloniki and large commercial teams in China. Its board hires medical information specialists, quality assurance and GMP audit managers, marketing leads, accountants, engineers and AI experience designers.

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:

  • 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

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
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