Sunpharma Hiring For Analytical Quality Assurance
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Sunpharma Hiring For Analytical Quality Assurance |
Department: Quality Assurance
Position: Manager - 1 - Analytical
Location: Dadra - Quality Control
Qualification: M.Sc. / M.Pharm. in Analytical Chemistry / Pharmaceutical Sciences or related field.
Experience: 8–12 years of experience in Analytical Quality Assurance in a regulated OSD manufacturing environment.
Key Responsibilities:
- Ensure compliance with cGMP, regulatory guidelines (USFDA, MHRA, EU, etc.), and company SOPs in analytical QA activities.
- Review and approve analytical documents such as COAs, raw data, instrument logs, and calibration records.
- Oversee review and trending of stability data and OOS/OOT investigations.
- Manage audit preparedness for regulatory inspections and customer audits, with a focus on laboratory systems.
- Coordinate with QC and production teams for timely release of RM, PM, intermediates, and finished products.
- Ensure data integrity practices in the laboratory and conduct periodic internal audits.
- Support qualification and validation of analytical instruments and methods.
- Monitor and review environmental monitoring and microbiological data related to laboratory operations (if applicable).
- Lead AQA team and ensure continual training and development of team members.
Key Skills:
- Strong knowledge of analytical techniques (HPLC, GC, UV, etc.) and regulatory expectations.
- Excellent understanding of laboratory quality systems and data integrity requirements.
- Good leadership, communication, and documentation skills.
- Analytical thinking and problem-solving ability.
- Proficiency in reviewing and interpreting analytical data.
How To Apply
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