Associate Quality Control Job at Pfizer | MSc Chemistry Jobs
Are you searching for high-growth Quality Control Jobs in the pharmaceutical industry? The Associate Quality Control Recruitment 2026 opportunity through Pfizer Careers offers an excellent role for professionals with expertise in analytical method validation, method transfer, and quality compliance. This position is ideal for candidates with an M.Sc. in Chemistry or Pharmacy who want to build a successful career in pharmaceutical quality systems, analytical testing, and regulatory compliance while working with one of the world’s leading healthcare organizations.
About the Company
Pfizer is a globally recognized biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that improve patient lives. With a strong focus on science, quality, and innovation, Pfizer maintains world-class manufacturing and quality systems across its global operations. Through Pfizer Careers, professionals gain opportunities to contribute to healthcare advancements while working in a culture driven by scientific excellence, compliance, collaboration, and continuous improvement.
Job Overview
Pfizer is hiring an Associate – Quality Control for its Vizag facility. This role focuses on analytical method transfer, validation, verification, and quality control testing activities in compliance with cGMP and regulatory requirements. The selected candidate will perform complex analytical testing using HPLC
, GC, UV-Vis, FTIR, Karl Fischer, and pH meter techniques. The role also involves documentation management, SOP review, analytical method validation as per ICH Q2 guidelines, and collaboration with cross-functional teams to support product quality and regulatory compliance. This is an excellent opportunity for professionals seeking advanced Pharmaceutical Quality Control Jobs and long-term growth in the pharmaceutical industry.- Job Post: Associate – Quality Control
- Locations: India – Vizag
- Job Requisition ID: 4955887
Responsibilities:
In this role, you will:
- Perform method transfers/validations/method verifications to the complex analytical techniques
- Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
- Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
- Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
- Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database.
- Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.
Requirements:
- Master’s degree in chemistry/ pharmacy with 2 – 5 years of experience in Analytical Method Transfer / Validation)
- Qualified in multiple analytical techniques (HPLC, GC, UV‑Vis, FTIR, Karl Fischer, and pH meters)
- Demonstrated technical skills in method validation and testing
- Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
- Conduct analytical method validation in accordance with ICH Q2 (R1/R2), USP, and EP standards, encompassing protocol preparation, execution, approval of validation summaries, and coordination with cross‑functional teams.
- Conduct test method GAP assessments against USP, EP, BP, and JP requirements for New Product Introduction (NPI).
- Execute and document analytical method verification and method transfer activities.
- Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
- Excellent organizational skills and strong ability to multi-task
- Strong written and verbal communication skills
- Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation
Preferred Requirements:
- Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography),GC techniques
- Proven track record in leading continuous improvement projects
- Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
- Strong problem-solving skills and attention to detail
- Ability to manage multiple priorities and meet deadlines.
- Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
- Adaptability and willingness to learn new techniques and procedures
The Associate Quality Control Recruitment 2026 opportunity at Pfizer Careers is an excellent choice for professionals seeking advancement in Quality Control Jobs and pharmaceutical analytics. With exposure to analytical method validation, regulatory compliance, advanced instrumentation, and global quality standards, this role provides significant career growth opportunities. Candidates with experience in HPLC, GC, method transfer, and quality systems are encouraged to apply and become part of an organization dedicated to delivering safe and effective healthcare solutions worldwide.
