Junior Team Member QC | Cipla Ltd | Bommasandra
Job Overview
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Date PostedApril 3, 2023
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Location (State / UT)
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Expiration date--
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Experience2 Years
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GenderAny
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Desired QualificationBachelor 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
