Procter & Gamble is the innovation leader in our industry. Virtually all the organic sales growth we’ve delivered in the past nine years has come from new brands and new or improved product innovation. We continually strengthen our innovation capability and pipeline by investing two times more, on average, than our major competitors. P&G. We interact with more than five million consumers each year in nearly 60 countries around the world.
Post : Process Owner
Job Description
• Responsible for Initiation of Stability study as per guidelines and compilation of stability study results after receipt of reports.
• Timely review of IP/BP/USP Pharmacopoeia & it's addendum / Errata / Annotated list / Amendment lists for RM/FP
• Change control initiation.
• Implementation of changes on or before Pharmacopeial Effective dates.
• Responsible for development activities & Compilation of P2P Dossiers.
• Responsible for creation of new Raw material parts, Formulation parts, Making Instructions and other technical documents in Enovia.
• Responsible for maintaining and updating stability data and other technical documents in ENOVIA- IRM.
• To support in creating / revising test masters, PFCs for FOP and RMP in Enovia.
• Responsible for creating Purchase requisition and service entries related activities in COUPA.
• Responsible for Inter-departmental coordination for smooth functioning of business.
• Timely raising of CC in GTRAQ for various pharmacopoeia changes as well as changes after validation activities.
• Timely completion of GTRAQ actions.
• Preparation of various SOPs in Veeva.
• Upgradation of laboratory documents as per GMP Requirement
• To support in preparation of Analytical Method Validation protocols and reports as and when required.
• To support in preparation of lab related or analysis related Deviations, OOS-OOT records.
• To prepare TT protocols and Reports.
• After TT, to raise GTRAQ as per requirement.
Candidate Profile
B.Pharm / M.Pharm / M.Sc. Chemistry (like Organic chemistry, Inorganic chemistry, Physical chemistry, analytical chemistry)
2 – 6 year experience in various documentation.
Additional Information
Experience : 2 – 6 year
Qualification : B.Pharm/ M.Pharm / M.Sc
Location : Mumbai, Maharashtra
Industry Type : Pharma
Functional Area : Supply Network Operations
End Date : 30th June, 2022
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