Manufacturing Chemist Job Vacancies in Mumbai

Key Responsibilities:Implement and monitor QA systems (as per GMP/ISO/FDA guidelines).Conduct internal audits and support external audits (regulatory & client).Review and approve SOPs, batch records, and quality documents.Investigate and document deviations, CAPA, OOS, and change controls.Coordinate with production, QC, and regulatory teams for compliance.Ensure training and qualification of QA team members.Maintain records and documentation per regulatory standards.

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.