Globela Pharma QA & QC Jobs in Surat – Freshers Can Apply
Globela Pharma QA & QC Jobs in Surat – Freshers Can Apply Published on: October 26,… Read More

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.
| 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 |
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.
| 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 |
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.
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.
| GMP Compliance | Validation |
| Documentation Review | SOP Review |
| Manufacturing QA | Risk Assessment |
| Investigation & CAPA | Attention to Detail |
| Communication | Quality Mindset |
This position was suited to candidates who:
Candidates seeking similar roles should review the experience and qualification criteria in each new vacancy before applying.
Applications should be submitted through the official Lupin recruitment portal.
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.
| 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. |
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.
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