Process Owner Job in Procter & Gamble

Responsible for end-to-end execution of business processes within Organization Units, Functions, Markets, etc. Responsible for process communication, deployment, and continual improvements. Provides direction and coaching to employees/leaders, as well as ensuring deadlines are met. Provides summary of outcomes, and after action review.

Key accountabilities:

• 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.

After TT, Validation data and Stability data to be upload in IRM as and when required

B. Pharm/ M.Pharm / M.Sc. Chemistry (like Organic chemistry, Inorganic chemistry, Physical chemistry, analytical chemistry)

2 6 year experience in various documentation.