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- ...Job Summary: The Quality Assurance (QA) Manager will be responsible for developing, implementing, and managing quality control systems to ensure that products or services meet established quality standards and regulatory requirements. This role involves leading a team of QA...Suggested
- ...harmonization efforts. Qualifications & Experience Education: B.Pharm / M.Pharm Experience: Minimum 8–15 years of experience in QA Documentation with Pharma Formulations Strong understanding of cGMP, QMS, and regulatory requirements (WHO, EU, etc.) Hands-on...Suggested
- To conduct and document analytical method validation (AMV), method verification, and method transfer activities for raw materials, in-process samples, and finished pharmaceutical products in compliance with ICH Q2(R1) , GMP , and regulatory standards . Key Responsibilities...Suggested
- ...development and documentation activities are conducted in accordance with cGMP, GLP, and global regulatory expectations. Collaborate with QA and Regulatory Affairs during internal and external audits, as well as during regulatory filings. Contribute to dossier preparation...SuggestedImmediate start
- Job Responsibilities Optimum machine availability, workforce & shifts of maintenance department, draw PPM plan & execute it. CGMP instructions to be followed, solve all technical issues, machine maintenance, care of safety & environmental pollution aspects, breakdown ...SuggestedShift work
