QA/QC Jobs

Lupin Officer – Quality Assurance Job in Pune

PC Pharma Career Updates Editorial Team · Oct 7, 2026 · 4 min read

Lupin Officer – Quality Assurance Job in Pune

Published on: 7 October 2026

Lupin has posted an Officer – Quality Assurance vacancy at its Pune Biotech facility, Maharashtra. The position covers quality activities related to drug substance manufacturing and warehouse operations.

This article is based on the official Lupin vacancy. Candidates should check the official listing before applying because recruitment information can change.

Current Status: Filled(Status Verified: 12 October 2026). The official Lupin recruitment page confirms that this position has been filled.

Candidates can visit the Lupin Careers portal to explore other vacancies.

1. Job Details

Detail Information
Company Lupin
Position Officer – Quality Assurance
Location Pune Biotech, Maharashtra
Experience 1–3 years
Qualification Master’s in Biotechnology; Post Graduation in Biopharmaceutics or Pharmacy
Job Function Quality Assurance
Posted On 7 October 2026
Job ID 1437620500
Salary Not disclosed
Vacancy Status Closed – Position Filled
Official Vacancy View Official Lupin Vacancy
Career Portal Explore Lupin Careers

2. About the QA Role

This position is based at Lupin’s Pune Biotech site and is focused on drug substance manufacturing and warehouse operations.

The role involves checking manufacturing and warehouse activities against GMP requirements, regulatory expectations and approved procedures. It also includes quality documentation, investigations, validation and quality-system activities.

Overall, this is a manufacturing-focused QA position with both operational and documentation responsibilities.

3. Key Responsibilities

Area Responsibilities
GMP Compliance Visit DS manufacturing and warehouse facilities and check activities against GMP, regulatory requirements and approved procedures
Investigations & CAPA Participate in manufacturing investigations and CAPA finalization
Risk Assessment Prepare and review risk assessments and mitigation plans
Validation Ensure process and cleaning validation follows approved protocols
Documentation Review study protocols, BPRs and MFRs
Batch Release Review executed BPRs for batch release
Dispatch Review Batch Dispatch Records and verify dispatch activity
APQR Coordinate APQR data compilation and preparation
Quality Systems Prepare and review Quality System SOPs
SOP Review Review departmental SOPs against GMP requirements

4. What the Role Means in Practice

In this role, Quality Assurance involves more than checking documents. The officer must help ensure that manufacturing and warehouse activities follow approved procedures and applicable GMP requirements.

For example, reviewing a Batch Production Record (BPR) involves checking completed manufacturing entries and confirming that required documentation is complete. During an investigation, the QA officer may help identify the cause of a deviation and follow up on corrective and preventive actions (CAPA).

The position also includes validation documentation, Annual Product Quality Review (APQR) activities and quality-system procedures.

5. Important Topics to Revise

Candidates interested in the role should have a practical understanding of the following areas:

Topic Key area to understand
GMP Basic requirements for compliant manufacturing
Deviation & Investigation Investigation process and root-cause analysis
CAPA Corrective and preventive actions
Risk Assessment Identifying and controlling quality risks
Process Validation Basic validation principles
Cleaning Validation Purpose and key concepts
BPR/MFR Manufacturing record review
APQR Purpose and basic requirements
SOPs Use and review of approved procedures
Batch Release QA review before batch release

For additional regulatory reference, candidates can consult the ICH Quality Guidelines, CDSCO and 21 CFR Part 211.

6. Relevant Skills

GMP Compliance Validation
Documentation Review SOP Review
Manufacturing QA Risk Assessment
Investigation & CAPA Attention to Detail
Communication Quality Mindset

7. Who Was This Role Suitable For?

This position was suited to candidates who:

  • Met the qualification requirements specified in the original vacancy.
  • Had 1–3 years of relevant experience.
  • Had an interest in manufacturing Quality Assurance at a biotech facility.
  • Had knowledge of GMP compliance, quality documentation and pharmaceutical quality systems.

Candidates seeking similar roles should review the experience and qualification criteria in each new vacancy before applying.

8. How to Apply

Applications should be submitted through the official Lupin recruitment portal.

  1. Open the Officer – Quality Assurance vacancy.
  2. Review the complete job description and requirements.
  3. Confirm that your qualification and experience match the listed criteria.
  4. Follow the application instructions provided on the vacancy page.
  5. Submit your application through the official recruitment system.

If the specific opening is no longer visible, candidates can check the Lupin Careers job search page for other current vacancies.

Important: Never pay anyone for a job application, interview or selection. Use Lupin’s official careers website to verify recruitment information.

9. FAQ

Question Answer
Where was the Lupin Officer – Quality Assurance position located? Pune Biotech, Maharashtra.
How much experience was required? 1–3 years, according to the published vacancy details.
What qualification was required? Master’s in Biotechnology or postgraduate qualification in Biopharmaceutics or Pharmacy, as listed in the vacancy details.
What type of work did the role involve? Manufacturing QA, GMP compliance, documentation, investigations, CAPA, validation and APQR.
Is this position still available? No. The official recruitment page confirms that the position has been filled.
Where can candidates find other Lupin vacancies? On the official Lupin Careers portal.

Related Resources

10. Final Takeaway

The Lupin Officer – Quality Assurance vacancy at Pune Biotech was intended for candidates with 1–3 years of experience and the specified postgraduate qualifications. The role covered manufacturing QA, GMP compliance, batch documentation, investigations, CAPA and validation.

The position has been filled and is no longer open for applications. Candidates can check Lupin’s official careers portal for other opportunities.

Disclaimer: Vacancy details are based on the published job information. Recruitment status and requirements may change; always verify details through the official company website.

PC

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