MQA Downstream Associate Manager

Grapevine Round1 AI; Visakhapatnam; On-site; INR 3,500,000 - 4,000,000; Full time

Job summary

Grapevine Round1 AI in Visakhapatnam is seeking an MQA Downstream Associate Manager. In this role, you will ensure cGMP compliance in critical operations within a pharmaceutical manufacturing environment.

Responsibilities include hands-on oversight, reviewing electronic batch records, assessing reports, and maintaining compliance standards. Candidates must possess 6-8 years of relevant experience and a strong understanding of quality assurance processes.

Qualifications

• 6-8 years of experience in MQA, QA, or Production.
• Knowledge of cGMP standards.
• Experience in eBR review.
• Ability to perform Acceptable Quality level sampling.
• Willingness to work in shifts.

Responsibilities

• Ensure cGMP compliance in terminal sterilization, visual inspection, and packaging operations.
• Oversee hands-on floor activities.
• Review electronic batch records.
• Assess batch reports.
• Analyze equipment breakdowns.

Skills

cGMP standards

eBR review

Quality assurance

Acceptable Quality level sampling

Tools

Batch reporting

Equipment audit trails

Job description

# MQA Downstream Associate ManagerPfizerVisakhapatnam, Andhra Pradesh, IndiaPosted 17 Jun 2026The MQA Downstream Associate Manager at Pfizer ensures cGMP compliance in terminal sterilization, visual inspection, and packaging operations. The role involves hands-on floor oversight, eBR review, batch report assessment, and equipment breakdown analysis. It requires expertise in quality assurance within a pharmaceutical manufacturing environment. The position is based in Visakhapatnam and involves shift work.Matched by TALApply to this role now. Install TAL for a 24/7 AI agent that keeps finding roles personalised for you.Apply nowInstall TALExperience6-8 yearsFunctionQuality AssuranceWork modeOnsite, IndiaCompanyTier 1## What you will work onThe MQA Downstream Associate Manager at Pfizer ensures cGMP compliance in terminal sterilization, visual inspection, and packaging operations. The role involves hands-on floor oversight, eBR review, batch report assessment, and equipment breakdown analysis. It requires expertise in quality assurance within a pharmaceutical manufacturing environment. The position is based in Visakhapatnam and involves shift work.## TAL's takeQuality 75/1005/5 clarityTier 1 companyStrong Tier 1 pharmaceutical company with a clearly defined quality management role in manufacturing.The JD provides a highly specific set of responsibilities related to terminal sterilization, visual inspection, and packing quality oversight.## Salaries at Pfizer22.3 LPA averageBased on 4 Grapevine salary entries for Pfizer.View all salariesOther roles2 - 4 years | 1000000-12000009 LPA averageRange: 9 - 9 LPAOther roles4 - 6 years | L15 LPA averageRange: 5 - 5 LPAOther roles6 - 8 years | Manager35 LPA averageRange: 35 - 35 LPAOther roles8 - 10 years40 LPA averageRange: 40 - 40 LPA## Must haves* 6-8 years of experience in MQA/QA/Production* Knowledge of cGMP standards* Experience in eBR review* Ability to perform Acceptable Quality level sampling* Ability to work in shifts## Tools and skillsmescgmpebrbatch reportingequipment audit trails