Junior Team Member – QC | Cipla Ltd | Sikkim, Rangpo

Manufacturing, QA/QC/QMS/IPQA/CQA
Sikkim
October 6, 2023
Full Time
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Job Overview

  • Date Posted
    October 6, 2023
  • Location (State / UT)
    Sikkim
  • Expiration date
    March 19, 2026
  • Experience
    2 Years
  • Gender
    Any
  • Desired Qualification
    Bachelor Degree, Master’s Degree

Job Description

Job Purpose

Prepare, update and review the specifications, SOPs, policy, and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards/pharmacopeia and cGMP requirements

Accountabilities

  • Prepare documents like SOPs, specifications, and non-routine documentation and ensure timely availability across the site to provide support during the analysis
  • Review the latest pharmacopeial updates, supplements, and amendments by evaluating the updates required in the available documentation to ensure compliance with the current pharmacopeia through consent from the regulatory body
  • Review the assigned documents by referring to the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements
  • Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit
  • Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed
Education Qualification

B. Pharma/ M.Sc

Relevant Work Experience

2 years of experience in the Quality Control department of a Pharmaceutical Organization

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