Cipla
Designation : Junior Team Member
Function : QC
Functional Area : Quality Control
Job Role Summary : 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
Job Profile :
- 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 document to ensure the compliance with the current pharmacopoeia through consent with regulatory body
- Document all activities performed as per valid procedure online by using standard/approved formats or templates to ensure that all entries done are correct, accurate and authentic
- 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
- Evaluate and prepare documents for standardization across all units at a site
Job Requirements :
1-3 years of experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms
Work / Job Experience : 1-3 Years
Type of Experience : Pharma QC experience in regulated industry
Academic Qualifications :
M.Sc. / B. Pharma.
