Pfizer Hiring QA Associate in Vizag (B.Pharm/M.Sc)
Pfizer Hiring QA Associate (Operations / Compliance / Investigations) in Vizag: B.Pharm, M.Pharm & M.Sc Candidates Can Apply
Pfizer is hiring an Associate for its Quality Assurance team, covering Operations, Compliance, and Investigations functions, at its manufacturing site in Vizag (Visakhapatnam), Andhra Pradesh. The role is full-time and open to candidates with a B.Pharm, M.Pharm, or M.Sc. background, with experience requirements set at 2 to 3 years for Master’s degree holders and 4 to 5 years for Bachelor’s degree holders. For quality professionals searching for pharma QA jobs in Andhra Pradesh, this is an opportunity to work within one of Pfizer’s key sterile manufacturing sites in India.
Company Overview
Pfizer is one of the world’s largest biopharmaceutical companies, working to translate advanced science and technology into therapies across multiple disease areas. In India, Pfizer Healthcare India Private Limited operates an export-oriented manufacturing unit at Vizag spanning more than 47 acres, dedicated to producing sterile injectables, including vials, emulsions, and ampoules, through a terminally sterilized manufacturing facility. The site is built around advanced technical capabilities such as automated solution compounding, clean-in-place and sterilize-in-place (CIP/SIP) systems, high-speed integrated fill-finish lines, and automated visual inspection and packaging lines with serialization support. This combination of scale and advanced manufacturing technology makes the Vizag site one of Pfizer’s significant quality-driven facilities in India, offering QA professionals direct exposure to a globally relevant, export-focused sterile manufacturing environment.
Job Role & Responsibilities
This Associate role supports execution and review activities across three connected areas of Quality Assurance.
Quality Operations
Responsibilities include reviewing QC documents such as BQ and CQ records, batch records, and related documentation, supporting shop-floor QA activities including GMP compliance monitoring and in-process checks, and reviewing SOPs, specifications, STPs, and study protocols to ensure they meet required quality standards.
Quality Compliance
The role involves supporting audit activities, inspection readiness, and regulatory commitments, while ensuring adherence to cGMP, GDP, and other regulatory requirements. The Associate will also support quality systems such as Change Control and CAPA tracking, and assist with data integrity and documentation control activities.
Quality Investigations
Core responsibilities here include supporting deviation investigations and CAPA implementation, assisting in root cause analysis using established investigation tools, tracking investigation closures within set timelines, and ensuring investigation records are properly documented.
Beyond these three areas, the role also calls for a fundamental understanding of manufacturing and quality control processes such as solution preparation, filling, sterilization, visual inspection, and packaging, along with knowledge of chemical and microbiology testing, strong interpersonal and decision-making skills, and the ability to work effectively across cross-functional teams.
Eligibility & Qualifications
Pfizer has outlined the following minimum requirements for this position:
- Educational qualification: B.Pharm, M.Pharm, or M.Sc.
- Experience: 2 to 3 years for Master’s degree holders, or 4 to 5 years for Bachelor’s degree holders
- Prior experience in Pharma or Biotech QA, QC, or Manufacturing functions
- Familiarity with Change Management processes and risk assessment principles and tools
- Exposure to validation of manufacturing equipment and Drug Product Process validations
- Strong knowledge of regulatory requirements, compendial changes, Good Documentation Practices, and Good Manufacturing Practices
- A thorough understanding of 21 CFR 211, along with Pfizer’s quality standards, site procedures, and processes
- Strong interpersonal and communication skills across all levels of the organisation
- A compliance-driven approach with solid working knowledge of cGMP and applicable regulations
- Experience or readiness to support national and international regulatory inspections, including USFDA, MHRA, TGA, and WHO
Location & Salary
This role is based at Pfizer’s manufacturing site in Vizag (Visakhapatnam), Andhra Pradesh. Pfizer has not disclosed a specific salary figure for this position. Based on prevailing compensation trends for QA Associate roles with 2 to 5 years of experience at large multinational pharmaceutical manufacturers in India, candidates can expect an estimated annual package in the range of ₹6 LPA to ₹11 LPA, depending on educational qualification, years of experience, and prior exposure to regulatory inspections and validation activities.
Application Process
Interested candidates can apply directly through Pfizer’s official Workday careers portal for this requisition.
Apply for Associate – Quality Assurance (Operations/Compliance/Investigations), Vizag
Candidates should ensure their resume clearly reflects relevant QA, QC, or manufacturing experience, along with any exposure to regulatory inspections, change control, CAPA, or validation activities, as these align directly with the core responsibilities of this role.
Why Join Pfizer?
- Opportunity to work at one of Pfizer’s significant sterile injectable manufacturing sites in India, built on advanced, globally relevant technology
- Direct exposure to quality operations, compliance, and investigation functions within a single, well-rounded QA role
- Experience working toward and supporting major international regulatory inspection standards, including USFDA, MHRA, TGA, and WHO
- A chance to build deep expertise in cGMP, CAPA, and validation processes within a globally recognised biopharmaceutical company
- Pfizer’s broader commitment to equal employment opportunity and a compliance-driven, integrity-led workplace culture
Frequently Asked Questions
What experience is required for this Pfizer QA Associate role? Candidates with a Master’s degree need 2 to 3 years of experience, while those with a Bachelor’s degree need 4 to 5 years of relevant experience in Pharma or Biotech QA, QC, or Manufacturing.
What educational qualification is required? A B.Pharm, M.Pharm, or M.Sc. degree is required for this role.
Where is this job located? The role is based at Pfizer’s manufacturing site in Vizag (Visakhapatnam), Andhra Pradesh.
What kind of regulatory knowledge is expected for this role? Candidates should have a thorough understanding of cGMP, GDP, 21 CFR 211, and Pfizer’s quality standards, along with the ability to support national and international inspections such as USFDA, MHRA, TGA, and WHO audits.
What is the expected salary for this role? Pfizer has not disclosed an exact figure. Based on industry trends for similar QA Associate roles, the estimated range is approximately ₹6 LPA to ₹11 LPA.
| Company | Pfizer (Pfizer Healthcare India Private Limited) |
| Vacancies | Associate – Quality Assurance (Operations/Compliance/Investigations) |
| Required Education | B.Pharm, M.Pharm, M.Sc. |
| Experience | Master’s Degree: 2–3 Years; Bachelor’s Degree: 4–5 Years |
To apply for this job please visit pfizer.wd1.myworkdayjobs.com.
