P&G Pharma & Chemistry Process Owner Vacancy 2022 - Apply Online

P&G Pharma & Chemistry Process Owner Vacancy 2022 – Apply Online

P&G Hiring chemistry and pharma candidates. B Pharma & M Pharma job opening 2022. MSc Chemistry job vacancy 2022. Candidates with bachelor’s degree in pharma and masters degree in chemistry may apply for the job opening at P&G. Process Owner job opening 2022. Check out all the details on the same below:

Job Title: Process Owner

Job locations: Mumbai, Maharashtra, India

Job Type: Full time

Job categories: Supply Network Operations/Logistics

Req No: R000051204

Elibgility Criteria:

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

Experience: 2 – 6 years of experience in various documentation.

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 a 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 to activities in COUPA.
  • Responsible for Inter-departmental coordination for smooth functioning of the business.
  • Timely raising of CC in GTRAQ for various pharmacopeia 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 the preparation of Analytical Method Validation protocols and reports as and when required.
  • To support in the 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.

Apply Online

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