JUBILANT Officer-Quality Assurance
Summary of Job
s(Purpose/ objective of the job Department organogram to be enclosed)
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- Document preparation, review, document control, compliance checks.
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Key Responsibilities
(Performance Indicators)
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- Responsible for preparation and use of SOP’s in all departments as per the laid down procedures.
- Responsible for online and facility audits of QC, Production, warehouse and engineering for GMP compliance.
- Responsible for the review of documents of manufacturing and testing before the release of product and approved labels for dispatch.
- Responsible for monitoring adherence to various cGMP activities and laid down procedures in receipt, storage, testing, processing and dispatch of products.
- Responsible for issuance and archival of batch manufacturing and testing records along with all second level documents till their retention period.
- Responsible for the retrieval of documents as and when required and ensure that current version of documents are available at work place.
- Preparation of approved vendor list.
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No. of Reportees
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NA
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Qualification & Experience
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- M.Sc Chemistry / 3-6 Years experience in API manufacturing unit.
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