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Job Overview

  • Date Posted
    December 25, 2022
  • Location (State / UT)
  • Expiration date
    --
  • Experience
    10 Years, 16 Years
  • Gender
    Any
  • Desired Qualification
    Bachelor Degree, Master’s Degree

Job Description

Roles and Responsibilities

Quality Control Activities :

  • Ensure the operational lab activities in a GMP manner
  • Timely release of RM, PM, Finished product, and Stability samples
  • Well aware-of lab software like LIMS, Lab Solution, Empower, etc
  • Investigation of OOS, OOT, and OOAL from a laboratory point of view
  • Provide training to lab analysts and troubleshoot

 

Quality Assurance Activities :

  • Planning, and organizing Qualification activities, review of documents like URS, Design documents, FAT, Qualification Protocol, SOP, and other GMP documents.
  • To review and approve change control, risk assessment, corrective and preventive action, involved in investigation and handling of deviations
  • Monitoring of IPQA Activities, QMS Activities, Stability sample, and Retaining sample Management
  • Monitoring and Managing documents issuance and document Control
  • Handle and participate in GMP audit and compliance report with the QMS system

Desired Candidate Profile

Desired qualification: B.Sc/M.Sc/B.Pharm/M.Pharm

Pharma experience: 10+ years