Mangalam Drugs & Organics Ltd. - Commenced its business in 1977 of manufacturing of chemicals such as perfumery, organic/inorganic chemicals, disperse dye intermediates, bulk drugs and bulk drugs intermediates at VAPI-Gujarat State. It has a multi-product manufacturing facility and a in-house Research and Development (R&D) Base.
Post: QA Executive
Job Description:
1. To supervise the QA activities of manufacturing plant.
2. To review and release the batch after referring manufacturing and control record.
3. To review distribute SOP related to all dept. & keep record and manufacturing activities.
4. To ensure the compliance of systems during manufacturing packaging of products.
5. To assist in investigation of market complaints.
6. To organize co-ordinate for self-inspection program across the facility.
7. To review protocol & report of validation programs.
8. To review and update Batch Manufacturing record format.
9. To review & check the BMR for its compliance as per the requirement.
10. To issue quality related formats to concerned departments
11. Change control closure & follow up.
Desired Profile:
Candidates must have atleast 4 - 7 years of experience in API / Bulk Drugs industry. Should have good knowledge of documentation of cGMP guidelines.
Additional Information:
Exp: 4-7 years
Location: Daman, Valsad, Vapi
Education: B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QA
Forward your resume at, career@mangalamdrugs.com
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