Lupin Manufacturing Solutions Walk-in Interview 2026 | QC, QA & Instrument Engineer Jobs in Vadodara
Lupin Manufacturing Solutions Ltd. has announced a Walk-in Interview for experienced Pharma professionals at Vadodara. Candidates having experience in Quality Control, QA Analytical Review, and QC Instrument Engineering can attend the interview directly on the scheduled date. Complete details including qualifications, experience, venue, registration link, and email are provided below.
Walk-in Interview Summary
| Organization Name | Lupin Gujarat Walk-In Interview on 25th July 2026 For Quality Control (QC), QA Analytical Review, QC Instrument Engineering Check here |
|---|---|
| Walk-in / Job Opening | Walk-in Interview 2026 |
| Location | Dabhasa Plant, Padra (Vadodara), Gujarat |
| Department | Quality Control (QC), QA Analytical Review, QC Instrument Engineering |
| Email ID | vinodparmar@lupin.com |
| Registration Link | Click Here for Registration |
Walk-in Interview Details
- Organization: Lupin Manufacturing Solutions Ltd.
- Plant: Dabhasa Plant, Padra (Vadodara)
- Interview Type: Walk-in Interview
- Date: 25th July 2026
- Time: 10:00 A.M. to 04:00 P.M.
- Venue: Baroda Productivity Council, BPC Road, Vadodara
Lupin Manufacturing Solutions is hiring experienced Pharma professionals for multiple Quality Control, QA, and Instrument Engineering positions. Candidates meeting the eligibility criteria can attend the walk-in interview directly with updated resume, educational documents, experience certificates, salary proof, Aadhaar Card and passport size photographs.
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Available Job Openings
- Quality Control – Jr. Officer / Officer
- QA Analytical Reviewer – Officer / Executive
- QC Instrument Engineer – Officer / Executive
Documents Required
- Updated Resume
- Passport Size Photographs
- Educational Certificates
- Experience Certificates
- Latest Salary Slip
- PAN Card
- Aadhaar Card
- Government Photo ID Proof
Continue with Part 2.
Quality Control – Jr. Officer / Officer
Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm with 3–6 years of experience in the Pharmaceutical Industry.
Required Experience
- Experience in handling analytical instruments like HPLC, GC etc.
- Experience of Wet Lab, Karl Fischer (KF), Auto Titrator, UV and IR instruments.
- Knowledge of GLP, CSV, QAMS and Laboratory Investigations.
- Exposure of working in QC shop floor for API plants inspected by USFDA, MHRA and TGA.
- Experience in Amino Acids and Polypeptides analysis.
- Working knowledge of LIMS for sample tracking and reporting.
- Analytical exposure on LC-MS, GC-MS, UPLC, ICP-MS, TGA and XRD.
The Quality Control team is looking for experienced Pharma professionals with strong analytical skills and knowledge of modern laboratory instruments. Candidates having regulatory exposure and API manufacturing experience will be preferred.
[ads id="ads1"]QA Analytical Reviewer – Officer / Executive
Qualification: M.Sc. / B.Pharm / M.Pharm with 4–8 years of experience in the Pharmaceutical Industry.
Required Experience
- Experience on analytical instruments like LCMS, GCMS, ICPMS, XRD and TGA.
- Hands-on experience with HPLC, GC, FTIR and UV instruments.
- Experience in reviewing software audit trails.
- Exposure to analytical method validation and analytical method transfer activities.
- Good drafting, communication and spoken English skills.
The QA Analytical Reviewer role requires professionals capable of reviewing analytical data, ensuring regulatory compliance, supporting method validation activities and maintaining data integrity as per GMP requirements.
Why Join Lupin Manufacturing Solutions?
- Excellent career opportunities in the Pharmaceutical industry.
- Opportunity to work in a USFDA approved manufacturing environment.
- Professional work culture.
- Career growth and learning opportunities.
- Exposure to advanced analytical technologies.
Candidates meeting the required qualifications and experience are encouraged to attend the walk-in interview with all necessary documents. Selection will be based on technical knowledge, experience and interview performance.
Continue with Part 3.
QC Instrument Engineer – Officer / Executive
Qualification: BE (Instrumentation/Electrical) or M.Sc. with 5–8 years of experience in the Pharmaceutical Industry.
Required Experience
- Breakdown maintenance of QC instruments like HPLC, GC and LCMS.
- Preventive maintenance of laboratory analytical systems.
- Inventory management of critical instrument spare parts.
- Investigation of instrument-related errors and implementation of CAPA.
- Hands-on experience in preventive and breakdown maintenance of critical instruments including HPLC, GC and LCMS.
- Basic knowledge of Analytical Laboratory operations and GMP requirements.
The QC Instrument Engineer position is suitable for experienced Instrumentation professionals having expertise in laboratory analytical equipment maintenance, troubleshooting, calibration support and compliance with Pharmaceutical GMP standards.
[ads id="ads1"]Important Information
- Freshers need not apply.
- Lupin Manufacturing Solutions does not charge any registration or interview fee.
- Carry updated Resume, Educational Certificates, Experience Certificates, Salary Slip, Aadhaar Card, PAN Card and Passport Size Photographs.
- Candidates should reach the venue before the reporting time for smooth registration.
Registration
Online Registration:
Click Here to Register
Contact Email
Email: vinodparmar@lupin.com
Interview Venue
Baroda Productivity Council (BPC)
BPC Road,
Vadodara,
Gujarat
Preferences / Compulsions
- Candidates should have secured 60% marks / First Class in the highest qualification.
- This condition may be relaxed for candidates having a minimum of 5 years post qualification experience.
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Disclaimer
This recruitment information is shared for educational and job information purposes only. The above details have been extracted from the official walk-in interview advertisement. Candidates are advised to verify all information from the official registration link and company communication before attending the interview. Industrial Guide is not responsible for any changes in schedule, eligibility criteria or recruitment process.
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