Job description
1) Well versed with pharmaceutical QMS systems at par with international regulatory requirements.
2) Conversant in handling Quality System apex documents like Site Master File, Validation Master Plan and Quality Manual.
3) Should have expertise specifically in API (synthetic and semi synthetic) and OSD facilities. Additionally, experience in sterile manufacturing quality assurance specific to engineering project management is preferred.
4) Hand on experience in Qualification and validation of equipment, utilities, facility and systems with team management capability
5) Versed with qualification and validation (URS, DQ,IQ,OQ,PQ) of equipment in API, OSD and sterile manufacturing. Preferred to have synthetic and semi synthetic (fermentation) manufacturing operation expertise. Conversant with peptide (Synthetic and recombinant methodology) manufacturing facility is recommended.
Experience: 10-15 yrs
Location: Bangalore
Openings: 02
Qualification: M.Pharm in Any Specialization, MS/M.Sc (Science) in Any Specialization
Interested kindly share profiles on prasad.n101@biocon.com / /anita.pachorkar101@biocon.com
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