Jubilant Pharmova Limited Hiring - Pharma Candidates Apply

Jubilant Pharmova Limited Hiring – Pharma Candidates Apply

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Job Title: Executive-Quality Assurance

Location: Nanjangud, IND

Eligbility Criteria & Experience:

  • M.Sc / B Pharma & BE Chemical Engineering.
  • 2-5 years in QC & QA in a formulation & API unit.

Skills Required:

Functional Skills:

  • Exposure of various Regulatory audits like USFDA, MHRA, TGA, MCC, ANVISA etc.
  • Knowledge of Validation like process validation, equipment qualification, Cleaning
  • Validation, HVAC & Water system.
  • Good knowledge of analytical (Instrumentation, Chemical & Microbiological)
  • Good knowledge of cGMP & cGLP
  • Good Knowledge of in process Quality Assurance Checks.

Behavioral Skills:

Having good analytical, communication & interpersonal skills.

Key Responsibility Include:

Incoming QC:

Review the raw material specification and standard test procedure (STP) in compliance with pharmacopoeia.
Review the Packaging material specification & STP in compliance with pharmacopoeia.

In Process QC:

  • Responsible for monitoring and ensuring on line review of batch manufacturing documents, batch packing documents.
  • Responsible for carrying out. In Process control tests, line clearances activities, sampling during process validations, cleaning validation, batch manufacturing, packing.
  • Responsible for monitoring adherence to various cGMP activities and laid down.
    procedures in receipt, storage, testing, processing and dispatch of products.

FG Inspection:

Review in process & finished product specification & standard test procedure in compliance with pharmacopoeia.

SOP Preparation:

Responsible for preparation of SOP’s of IPQA.

GTP Review:

Review of GTPs.

Document Review:

  • Review the analytical method validation document.
  • Review the analytical method transfer document.
  • Review of Process validation, cleaning validation and Equipment qualification documents.
  • Review the stability data intended to regulatory submission.
  • Review of batch manufacturing & batch packaging record intended to regulatory filing.
  • Review the analytical document intended to regulatory submission.

Apply Online

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