Acme Formulation Recruitment 2019- :Acme Formulation Recruitment 2019 for the position of Head Quality Assurance .Please go through following summary of vacancy. Please check at bottom of the this Summary of vacancy for more details and apply on source web page.
|Post Name||Head Quality Assurance|
|Salary||14,00,000 – 24,00,000 PA.|
|Time & Venue||
Opening date: 22/07/2019
Job Description: -To ensure cGMP Compliance in the plant. 2. To review and approve all departments Standard operating Procedure. 3. To ensure for the compliance of all Standard operating Procedure. 4. Strategic Planning & execution of Quality Management System. 5. To ensure the compliance of Quality Management system as per the requirement. 6. Responsible for leading the external audit & providing the compliance in timely manner. 7. To review and approve the Site Manager File (SMF),Validation Master Plan(VMP) and Quality manual. 8. Responsible for the approval and release of the Batch. 9. To review & approve specifications, Standard Test Procedure (STP) and General Test Procedure (GTP) of Quality Control Department. 10. Responsible for Self Inspection or Internal Audit and its compliance. 11. To review and approve all Validation and Qualification Protocols and Reports. 12. To ensure the compliance of Vendor Audits and approval of Contract Laboratory. 13. To perform laundry audits in coordination with HR department. 14. To impart training on different topics including cGMP and GDP etc. 15. To coordinate during technology transfer of products to the sites. 16. To ensure that products are manufactured as per approved procedure. 17. Responsible for the investigation of the market complaints, Product recall & its compliances. 18. Responsible for review, approval and implementation and verification of Corrective Action and Preventive Action. 19. To provide the compliance reports of audits. 20. To give the final approval for Art Works. 21. To conduct interview and recruitments of Quality Assurance Personnel. 22. To ensure the Qualification and Re-qualification of the Equipment ,Facility and System 23. Responsible for review and approval of Stability Protocol and report. 24. To ensure work discipline in the department. 25. Responsible for quality agreement and its compliance. 26. To review and approve all apex documents
About Company :A Leading Pharma Group with Global Presence and approvals from EU-GMP, MHRA-UK, ANVISA Brazil, PICS Ukraine, WHO Geneva, INVIMA Colombia, USFDA* We have 3 facilities in North India and 1 R&D centre at Bengaluru , 1. Immacule Lifesciences- Manufacturing of Liquid and Lyophillized injections approved from MHRA, ANVISA, PICS Ukraine, USFDA. 2. Acme Formulation Pvt Ltd- Comprises of 2 blocks (General & Hormone) , manufacturing Tablets, Capsules approved by WHO Geneva, INVIMA & EU GMP. 3. Acme Generics LLP – Comprises of 2 blocks (General & Thyroxine) , manufacturing Tablets, Capsules approved by EU-GMP