12 - 18 years
10 - 13 Lacs
Posted:-1 days ago|
Platform:
Work from Office
Full Time
1. Responsible for the smooth functioning of the Quality control department and day-to-day monitoring of routine jobs.
2. To maintain the department as per GLP/Schedule M.
3. To allocate work to the QC chemist on a daily basis.
4. Checking / Verification of MRN of all incoming Raw material /packing material and sample intimation of bulk
and finish the product.
5. Approval or rejection of raw material, packaging materials, bulk, and finished products in relation to their specifications.
6. Monitoring the analysis activity carried out in the QC Lab and in the outside contact lab.
7. Ensure stability studies are performed on finished products at appropriate intervals as per protocols, and review.
the stability summary and certification of documents.
8. Ensure review and compliance with the regulatory guidelines and update the documentation for sampling.
inspecting and analysis carried out in the QC Lab.
9. Approval of Standard Operating Procedures, specifications, standard testing procedures, and other documents
related to Quality Control Procedures.
10. Ensure that all validation activity in the QC Lab is performed as per a defined schedule.
11. Participation in the internal and external audit.
12. Ensure the availability of adequate facilities, trained personnel, and approved procedures for sampling,
testing of raw material, packaging materials, and bulk and finished products.
13. To participate in the investigation of complaints related to the quality of the product.
14. Ensure evaluation, maintenance, and storage of the Pharmacopoeia, reference standards, and working standards.
15. Participation in QRM programs.
16. Ensure that any changes in documents are handled with appropriate QMS tools.
17. To facilitate & develop the team.
18. To ensure that the required initial and continuing training of quality unit personnel is carried out and
adapted according to need.
19. Ensure proper culture maintenance in the microbiology lab.
20. Participation in external lab audit and review of outside testing report.
A highly skilled and results-driven Quality Control Manager with an MSc in Pharmaceutical Sciences and over 14-18 years of experience in ensuring the highest standards of quality and compliance in pharmaceutical production. Adept at leading teams, streamlining processes, and implementing rigorous testing protocols to ensure product safety, efficacy, and regulatory compliance. Proven track record in managing cross-functional projects and driving continuous improvement in quality systems. Passionate about maintaining the highest quality standards in every stage of pharmaceutical development and manufacturing.
G S Pharmbutor Private Limited
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