Summary
Compensation: http://www.digvijaya.com
Education: UG - B.Sc - Chemistry PG - M.Sc - Chemistry
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Production, Maintenance, Quality
Desired Candidate Profile
Candidates should be M.Sc with 3 - 5 yrs exp. from a reputed bulk drug industry.
Job DescriptionGet involved in all quality related matters.
Review completed Batch Production and Control Records and Laboratory Records before release of the batches.
Investigate and resolve critical deviations.
Review, Approval of SOPs, Qualification, Validation, Protocols/Reports.
Approval of Specification, Test Procedures and Master Production Control Records.
Perform internal audit to verify compliance with the GMP for APIs.
Approve contract testing laboratories and vendors for raw materials.
hange control management.
Ensure the quality of raw material, in-process material, intermediates, packing material, and finished product as per the specifications and issue the certificate of analysis.
Maintain the analytical instruments in working conditions.
Provide training on cGMP/GLP and quality topics.
Ensure the timely analysis of samples.
Plan for stability study of APIs.
Plan for water analysis.
Updating Validation Master Plan.
Keywords: Quality Control, HPLC / GC etc
Company ProfileFor a reputed client of Digvijaya - Exclusive recruitment consultants for Pharma/Biotech/CROs.
Contact Details Company Name: DIGVIJAYA MANAGEMENT CONSULTANTS PVT.LTD.,
Address: 4D, 4th Floor, Nandanavanam, SR Nagar 'X' Roads,
HYDERABAD,Andhra Pradesh,India 500038
Telephone: 91-40-23817576