CIPLA Career Opportunities: Junior Team Member – QC M.Sc. / B. Pharma Apply Now
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
I. Prepare documents like SOPs, specifications and
non-routine documentation and ensure timely availability across the site to
provide support during the analysis
II. 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
III. Review the assigned documents by referring the
concern backup and pre-defined quality procedure to ensure its compliance
against the quality requirements
IV. 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
V. Execute harmonization and simplification process of
documents to reduce complexities in processes and ensure standardized
procedures are followed
Education Qualification
M.Sc. / B. Pharma
Relevant Work Experience
2 years of experience in QC department of a
pharmaceutical organization
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