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Pfizer Associate Manager – Quality Investigation Job in Vizag, Andhra Pradesh
Published on: November 1, 2026
Pfizer is inviting applications for the position of Associate Manager – Quality Investigation at its pharmaceutical manufacturing site in Vizag, Andhra Pradesh. The role focuses on microbiological investigations, deviation management, root cause analysis and CAPA review.
This opportunity is relevant to experienced B.Pharm, M.Pharm, M.Sc. Microbiology and Biotechnology professionals with at least 6 years of relevant experience.
Candidates interested in developing their knowledge of pharmaceutical quality systems can also try our Free QA and QC Mock Tests to practice subject-related questions.
1. Pfizer Recruitment 2026 – Job Overview
| Particulars | Details |
|---|---|
| Company | Pfizer |
| Job Role | Associate Manager – Quality Investigation |
| Job ID | 4966352 |
| Department | Quality Assurance |
| Job Location | Vizag, Andhra Pradesh |
| Qualification | B.Pharm, M.Pharm, M.Sc. or related discipline |
| Experience | 6+ years |
| Employment Type | Full-time |
| Work Arrangement | On-site |
| Application Mode | Online |
| Official Application | Apply Here |
Explore More Opportunities: Visit Pfizer Careers to search for other openings in Quality Assurance, Manufacturing, Regulatory Affairs and additional departments.
2. Educational Qualification and Experience
Pfizer accepts candidates from the following educational backgrounds:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- M.Sc. Microbiology
- Biotechnology
- Pharmaceutical Sciences or a related discipline
Experience requirement: A minimum of 6 years of experience in sterile pharmaceutical manufacturing, microbiology, Quality Assurance or investigation management.
Candidates should have relevant practical exposure to pharmaceutical quality investigations and GMP-related activities.
3. Job Responsibilities
The selected candidate will independently review and challenge microbiological investigations to ensure that conclusions are scientifically justified and meet regulatory expectations.
| Area | Key Responsibilities |
|---|---|
| Microbiological Investigations | Review deviations, OOS/OOT, contamination events, environmental monitoring excursions and sterility assurance investigations. |
| Root Cause Analysis | Evaluate investigation findings using 5-Why, Fishbone Analysis and Fault Tree Analysis. |
| CAPA Management | Review corrective and preventive actions and assess their ability to prevent recurrence. |
| Risk Assessment | Evaluate product quality, process, patient safety and compliance risks. |
| GMP Compliance | Ensure investigations follow cGMP requirements and applicable regulatory expectations. |
| Team Coordination | Work with Microbiology, Manufacturing, Engineering, Validation and Quality teams. |
| Technical Guidance | Coach investigation owners on scientific reasoning, critical thinking and technical report writing. |
| Continuous Improvement | Identify recurring deviations and opportunities to strengthen quality systems. |
4. Required Skills
Applicants should have knowledge and experience in the following areas:
| Technical Skills | Professional Skills |
|---|---|
| Quality Assurance and QMS | Critical thinking |
| Microbiological investigations | Problem-solving |
| Root Cause Analysis | Scientific decision-making |
| CAPA management | Effective communication |
| Risk management | Analytical skills |
| Data integrity | Team collaboration |
| GMP and regulatory compliance | Technical report review |
Knowledge of international regulatory requirements and GMP expectations is relevant to this position. Applicants should be familiar with guidance and standards issued by major regulatory organisations, including the US Food and Drug Administration (USFDA), European Medicines Agency (EMA), UK Medicines and Healthcare products Regulatory Agency (MHRA), Pharmaceutical Inspection Co-operation Scheme (PIC/S) and World Health Organization (WHO).
5. Who Should Apply?
This position is intended for experienced professionals who can independently evaluate complex pharmaceutical quality investigations.
It may be suitable for:
- QA professionals working in sterile pharmaceutical manufacturing.
- Microbiology professionals handling contamination and environmental monitoring investigations.
- Quality professionals experienced in deviation and CAPA management.
- Investigation reviewers with knowledge of GMP documentation and root cause analysis.
Candidates should highlight their experience with microbiological investigations, investigation report review, CAPA effectiveness and quality system improvements in their resumes.
Freshers and candidates without the required relevant experience may not meet the eligibility criteria.
6. How to Apply for Pfizer Jobs?
Interested and eligible candidates can submit their applications online through Pfizer’s official careers portal.
- Open the official job application link provided below.
- Review the complete job description and eligibility requirements.
- Sign in or create an account on the recruitment portal, if required.
- Enter your educational and professional details.
- Upload your updated resume and submit the application.
Apply Here: Pfizer Associate Manager – Quality Investigation (Job ID: 4966352)
Search More Jobs at Pfizer: Visit Pfizer’s Official Careers Page to explore other vacancies across Quality Assurance, Quality Control, Regulatory Affairs, Manufacturing and other departments.
Candidates should check the official job listing for the latest application status and recruitment updates.
7. Related QA/QC Career Resources
Looking for more opportunities and learning resources in pharmaceutical Quality Assurance and Quality Control? Explore these pages on PharmaCareerUpdates.com:
- QA/QC Jobs – Latest Pharmaceutical Vacancies – Find job updates in QA, QC and related departments.
- Career in Quality Assurance (QA) After B.Pharm – Understand career opportunities, job roles, skills and qualifications in pharmaceutical QA.
- Free Pharma Mock Tests – Practice subject-wise MCQs and assess your preparation.
8. Frequently Asked Questions
1. What is the job role at Pfizer?
Pfizer is recruiting an Associate Manager – Quality Investigation for its Vizag location.
2. What is the minimum experience required?
Candidates need at least 6 years of relevant experience in sterile pharmaceutical manufacturing, microbiology, Quality Assurance or investigation management.
3. Can B.Pharm candidates apply?
Yes. B.Pharm is an accepted qualification, provided applicants also meet the experience requirements.
4. Is this vacancy suitable for freshers?
No. The position requires a minimum of 6 years of relevant professional experience.
5. Where is the job located?
The position is based in Vizag, Andhra Pradesh, India.
6. Has Pfizer announced the salary for this position?
The salary is not specified in the official job listing. Candidates can check the recruitment portal for any additional information.
Disclaimer
PharmaCareerUpdates.com is an independent pharmaceutical job information platform and is not affiliated with, associated with or endorsed by Pfizer. Job details are shared for informational purposes only and are based on the company’s official careers listing. Recruitment requirements, application availability and other details may change at the employer’s discretion. Candidates are advised to verify all information on Pfizer’s official careers website before applying.
