|
. | DESIGNATION | MANAGER (QUALITY ASSURANCE) | | Experience | 10-15 years in Pharmaceutical industry | | Education | B.Pharm/M.Pharm/M.Sc (Organic/Analytical Chemistry) | | Location | Nagpur | | Remuneration | Best in Industry | | Job Responsibilities | Preferably working with Parenteral / Solid dosage manufacturing plant, responsible for conducting audits in plant, to implement cGMP system, to train QA personnels, monitoring of QA functions, to ensure that pharmaceutical products manufactured by the company meets the quality standards, Responsible for preparation, approval and compliances of following documents and records 1) Standard Operating Procedures. 2) Protocols (Process Validation, Equipment Validation and stability). 3) Annual Product Review. 4) Vendor Approval (RM and PM) | | Forward your Resume to
This e-mail address is being protected from spam bots, you need JavaScript enabled to view it
| | DESIGNATION | QUALITY ASSURANCE OFFICER | | Experience | Min. 1 year, fresher may also apply. | | Education | B. Pharm / M. Pharm | | Location | Nagpur | | Remuneration | Best in Industry | | Job Responsibilities | - Providing in-process Support to Production and QC.
- Preparation of MFR, Process Validation, Analytical Method Validation, Annual Product Review, Preparation & Checking of Art work,
- Preparation of STPs and Specification of RM, PM, Bulk & Finished Product.
- Auditing departments for implementation of GMP.
- To check manufacturing & in process records as per Master Formula Record.
- Responsible for GMP Implementation.
| | Forward your Resume to
This e-mail address is being protected from spam bots, you need JavaScript enabled to view it
| Note: Applicants should mention post applied for in the subject line.
|