Job Description

Manufacturing site and Product evaluation and approval for new sites/new products/ transfer of products from one site to another site.
o Ensure Good manufacturing practices and Compliances as per regulatory requirement at contract manufacturing site.
o Coordination with Supply Chain, Marketing, R&D and Production for new products, material destruction, batch disposition and other technical issues on day to day basis.
o To maintain a calendar and conduct periodic audits at existing sites for monitoring of cGMP compliance and CAPA implementation.
o Review of response of market complaint investigation and CAPA proposals.
o To provide feedback to the site. In case of critical complaint or where the cause could not be identified , to conduct for cause audits for identification of root cause and CAPA implementation
o Plan day to day activity for self and team members, in concurrence to complete the targeted audits, visits, joint analysis, investigation, CAPA verification and any other activities
o Review and approval of change controls initiated from F&D, ADL and artwork revision.
o Review and approval of quality events from respective loan license and third party manufacturing sites.
o Preparation and execution of process validation protocols and reports for new/transferred products, manufactured at loan license sites.

Role:QA / QC - Manager

Function:Quality Assurance / Quality Control (QA / QC)

Industry Category:Pharmaceuticals

Sub Category:Any

Job Type:Full Time

Job Reference ID:Zydus-001

Total Openings:1

Salary:9 to 14 Lakhs

Location:Hyderabad/Secunderabad

Job Qualifications

Please refer to the Job description above

Education (Specialization): Bachelor of Pharmacy (B.Pharma.) -Pharmacy,Master of Pharmacy (M.Pharma.)-Pharmacy,Master of Science (M.Sc.)-Chemistry

Experience:8 to 13 Yrs

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