0 years

1 - 2 Lacs

Posted:5 days ago| Platform: GlassDoor logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • Assist in gathering and reviewing documentation for vendor qualification and requalification.
  • Maintain approved vendor lists and vendor-related records.
  • Coordinate with suppliers for completion of questionnaires and other qualification documents.
  • Prepare and review Certificates of Analysis (CoA) for raw materials, intermediates, and finished products.
  • Compile and organize stability study data and summaries.
  • Support the preparation and maintenance of Drug Master Files (DMFs) and related documentation for regulatory submissions.
  • Ensure accuracy and completeness of quality-related records and logs.
  • Maintain electronic and physical filing systems.
  • Support trending and data analysis for quality metrics when required.
  • Coordinate with QA, QC, RA, and Production teams for timely documentation and data flow.
  • Assist in training staff on document control and QA procedures when necessary.

Job Type: Full-time

Pay: ₹10,447.57 - ₹20,000.00 per month

Work Location: In person

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