Eris Therapeutics Limited is fast growing pharmaceutical company (A Subsidiary of Eris lifesciences Limited).

Post : Sr. Executive / Assistant Manager – Production QMS

Location : Bavla, Gujarat
Industry : Pharmaceutical Formulations
Experience : 7–15 years

Key Responsibilities
• Drive effective implementation of Production QMS & cGMP compliance.
• Prepare, review and ensure timely completion of BMR/BPR, SOPs, logbooks and GMP records.
• Manage Deviations, CAPA, Change Controls, OOS/OOT and investigations.
• Support internal, customer and regulatory audits and ensure timely observation closure.
• Ensure GDP & Data Integrity compliance across production documentation.
• Identify recurring deviations and documentation gaps through trend analysis.
• Coordinate with QA, QC, Warehouse, Engineering and other functions.
• Conduct GMP/QMS training for Production personnel.
• Ensure effective employee induction and on-the-job training.
• Drive continuous improvement in compliance, documentation and operational excellence.

Key Skills
1. Production QMS
2. cGMP Compliance
3. BMR/BPR Documentation
4. Deviation Management
5. CAPA & Root Cause Analysis
6. Change Control
7. OOS/OOT Investigation
8. Data Integrity & GDP
9. Regulatory Audit Readiness
10. Cross-functional Leadership

Work Location
Eris Therapeutics Inc.
Plot No. 1231036, Village Kalyanegath,
Opp. Audi Auto, Bavla, Ahmedabad – 382220, Gujarat.

Qualification : B.Pharm / M.Pharm / B.Sc. / M.Sc. or equivalent pharmaceutical qualification.
Candidates with hands-on exposure to OSD, Liquid, External or Sterile manufacturing will be preferred.

Apply Now Email : [email protected]

Last Date : 10th October 2026