Aculife Healthcare Pvt. Ltd. (formerly known as “nirlife”), a part of the prestigious Nirma Group, is conducting a walk-in interview for its sterile manufacturing facility. We are seeking experienced professionals for our Quality Assurance (QA) Department to fill roles from Officer to Executive levels.

Walk-in Interview Details

Date: Saturday, December 27, 2025

Time: 08:00 AM to 11:00 AM

Venue: Aculife Healthcare Private Limited, Near Railway Crossing (Sanand – Viramgam Highway), Village: Sachana, Taluka: Viramgam, District: Ahmedabad – 382 150.

Current Job Openings in QA

1) Validation:

Exp: 2-5 Yrs

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

Designation: Officer to Executive

Job Description:

Key duties include developing IQ/OQ/PQ protocol, managing change controls, handling deviations, training teams, and ensuring data integrity for sterile manufacturing. Develop, execute, and review validation protocols for sterilization processes (autoclaves, gamma, ETO) and aseptic processes (Media Fills). Prepare, approve, and approve SOPs, validation reports, and batch records, ensuring GDP (Good Documentation Practises) and data integrity.

2) Lab-QA

Experience: 2-5 Yrs

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

Designation: Officer to Executive

Job Description:

• Outlines a role focused on maintaining product quality and compliance through testing, documentation, and process adherence, involving testing materials (raw, in-process, finished), calibrating equipment, following SOPs (cGMP/GLP), auditing troubleshooting issues, reporting data, and ensuring standards are met in industries like pharma, food, or cannabis.
• Key responsibilities include performing analyses, maintaining lab cleanliness, and supporting audits for safety and integrity.
• Ensure laboratory activities comply with cGMP, EU GMP, FDA, and data integrity requirements.
• Laboratory deviations, OOS, OOT, and investigations CAPA related to lab operations.
• Change controls impacting QC labs.

3) QMS

Experience: 2-5 Yrs

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

Designation: Officer to Executive

• Job Description:
• Develop, implement, and maintain QMS elements for sterile manufacturing (aseptic processing, terminal sterilization).
• Ensure compliance with cGMP, EU GMP Annex 11, FDA, ICH, and WHO requirements.
• Own and manage core QMS processes:
• Deviations/investigations, CAPA, Change Control, Risk Management (ICH Q9), Document Control, Training System, OOS/OOT, Product Quality Review (PQR/APQR).

4) IPQA

Experience : 2-5 Yrs

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

Designation: Officer to Executive

• Job Description:
• Perform line clearance and ensure readiness before the start of manufacturing, filling, and packing operations in sterile areas.
• Monitor aseptic processing activities, including gowning, environmental conditions, and adherence to SOPs during operations.
• Perform in-process checks such as volume, weight, leak test, particulate matter check, and integrity testing for sterile products.
• Ensure real-time documentation of batch manufacturing records (BMR), batch packing records (BPR), and logbooks.
• Verify cleaning and sanitization activities of sterile areas (Grade A/B/C/D).
• Ensure timely compliance with standard operating procedures (SOP), batches, and regulatory guidelines.
• Assist in investigations of deviations, out-of-specifications (OOS), and out-of-trend (OOT) results.