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Aculife Healthcare Private Limited, a prominent member of the Nirma Group, has announced an upcoming walk-in interview drive for its Quality Assurance (QA) department. This is a significant opportunity for pharmaceutical professionals looking to advance their careers in a sterile manufacturing environment.
Interview Schedule & Location
The recruitment event is scheduled for Saturday, December 27, 2025. Interested candidates should arrive between 08:00 AM and 11:00 AM to participate in the process.
Venue Details:
Aculife Healthcare Private Limited (formerly known as “nirlife”)
Near Railway Crossing (Sanand – Viramgam Highway)
Village: Sachana, Taluka: Viramgam
District: Ahmedabad – 382 150
Available Positions and Qualifications
Aculife is looking for experienced individuals for the designation of Officer to Executive across four specialized QA functions. All roles require a qualification of B.Sc., M.Sc., B.Pharm, or M.Pharm, along with 2 to 5 years of relevant experience.
1. Validation
Candidates will be responsible for developing IQ/OQ/PQ protocols and managing change controls and deviations. The role involves executing validation protocols for sterilization processes (autoclaves, gamma, ETO) and aseptic media fills. Ensuring Good Documentation Practices (GDP) and data integrity is a core requirement.
2. Lab-QA
This role focuses on maintaining product quality through rigorous testing and compliance. Responsibilities include ensuring lab activities meet cGMP, EU GMP, and FDA standards. Candidates will handle laboratory deviations, OOS (Out of Specification), OOT (Out of Trend) investigations, and CAPA related to lab operations.
3. QMS (Quality Management Systems)
The QMS team will develop and maintain quality elements for sterile manufacturing. Key tasks include managing core processes like Risk Management (ICH Q9), Change Control, Document Control, and Product Quality Reviews (PQR/APQR) while ensuring compliance with WHO and Annex 1 requirements.
4. IPQA (In-Process Quality Assurance)
IPQA officers will perform line clearances and monitor aseptic processing activities, including gowning and environmental conditions. The role requires performing in-process checks (volume, weight, leak tests) and ensuring real-time documentation of Batch Manufacturing Records (BMR) and logbooks.
How to Apply
If you are a qualified professional meeting the experience criteria, you are encouraged to attend the walk-in interview with your updated resume and relevant documents.
Unable to attend?
If you cannot make it to the venue on December 27, you can still apply by sharing your CV via email to:
- recruitment@aculife.co.in
- rajeshthakor@aculife.co.in
