- Documentation & Compliance:
- Maintain accurate and complete laboratory records in compliance with Good Laboratory Practices (GLP) and Positive Manufacturing Practices (GMP).
- Prepare and review Certificates of Analysis (CoAs), test reports, and deviation reports.
- Ensure compliance with company SOPs, safety protocols, and regulatory requirements (e.g., FDA, EPA, ISO).
- Process Validation & Improvement:
- Participate in validation of test methods and instruments.
- Assist in internal audits and support corrective and preventive action (CAPA) activities.
- Collaborate with R&D;, production, and other departments on quality-related issues
📌 QA Chemist for Palanpur
🏢 Pramukh Staffing
📍 Palanpur
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