Aculife Healthcare Pvt. Ltd Company is a part of USD 3 billion Nirma Group & it is one of world’s largest Infusion & Injectable Company, having a State-of-the art manufacturing facility spread over 550 acres of land located near Ahmedabad, Gujarat. Aculife healthcare has global operation in more than 100 countries and it has subsidiaries in Brazil, Mexico & Vietnam.
HIRING FOR QA DEPARTMENT
Post : Officer to Executive
Experience : 2 to 5 years
Qualification : MPharm, BPharm or MSc, BSc
Validation Department
Job Description : Key duties include developing IQ/OQ/PQ protocols, 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, review, and approve SOPs, validation reports, and batch records, ensuring GDP (Good Documentation Practices) and data integrity.
Lab-QA Department
Job Description : Outlines a role focused on maintaining product quality and compliance through testing, documentation, and process adherence, involving tasks like testing materials (raw, in-process. finished), calibrating equipment, following SOPs (like GMP/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
QMS Department
Job Description : Develop, implement, and maintain QMS elements for sterile manufacturing (aseptic processing, terminal sterilization). Ensure compliance with cGMP, EU GMP (Annex 1), FDA, ICH, and WHO requirements.
Own and manage core QMS processes:
Deviations / Investigations CAPA
Change Control
Risk Management (ICH 09)
Document Control Training System OOS / OOT
Product Quality Review (PQR/APQR)
IPQA Department
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 8MR), batch packing records (BPR), and logbooks.
Verify cleaning and sanitization activities of sterile areas (Grade A/B/C/D). Ensure timely review and compliance with standard operating procedures (SOPs), batch records, and regulatory guidelines.
Assist in investigations of deviations, out-of-specifications (OOS), and out-of-trend (OOT) results
Walk in Interview
Date : 27, Dec 2025 (Saturday)
Time : 08:00 to 11:00 am
Venue : ACULIFE HEALTHCARE PRIVATE LIMITED.
FORMALLY KNOWN AS “NIRLIFE”
NEAR RAILWAY CROSSING (SANAND - VIRAMCAM HIGHWAY)
VILLAGE : SACHANA,
TALUKA : VIRAMCAM
DISTRICT: AHMEDABAD - 382150
If you are unable to attend interview than share your CV : recruitment@aculife.co.in ; rajeshthakor@aculife.co.in
See All Ahmedabad Alerts B.Pharm Alerts M.Pharm Alerts M.Sc Alerts
See All Other Jobs in our Database
Subscribe to Pharmatutor Job Alerts by Email
