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Officer/Sr. Officer
2 weeks ago
Interested candidates are requested to share their resumes at for interview scheduling on 7th September 2025 at Hotel Ginger, Bharuch. Please note that it is mandatory to pre-schedule the interview before reporting at the venue.
Key Responsibilities:
- Perform routine and non-routine analysis of raw materials, intermediates, finished products, and stability samples related to SVP.
- Execute and document activities related to Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) as per approved protocols.
- Conduct instrument handling, calibration, and troubleshooting for analytical techniques such as HPLC, GC, Dissolution, UV-Vis, FTIR, and other QC instruments.
- Prepare, review, and maintain analytical test procedures, protocols, and reports in compliance with regulatory requirements.
- Ensure accurate documentation in laboratory records, logbooks, and LIMS systems in line with data integrity principles.
- Support regulatory audits and inspections by providing required analytical documents and justifications.
- Comply with all Good Laboratory Practices (GLP), Good Manufacturing Practices (cGMP), and EHS requirements.
- Participate in OOS/OOT investigations, deviation handling, and CAPA implementation.
- Collaborate with cross-functional teams for technology transfer and product scale-up related to SVP formulations.
Key Skills:
- Analytical Method Validation & Transfer
- Sterile/Parenteral QC Testing
- HPLC/GC/UV handling
- Regulatory & cGMP compliance
- Documentation & Data Integrity
- Problem Solving & Investigation Support