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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