DAMAN · FULLTIME
QA - Documentation- Officer
USV
Daman · onsite · Posted 9d ago
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Section · 01
About this role
- Assist in managing QMS documentation by drafting, routing for review, and safely archiving Standard Operating Procedures (SOPs) and quality manuals to ensure proper version control.
- Support the tracking of quality events by accurately logging deviations, Change Controls, and CAPAs (Corrective and Preventive Actions) into the system and monitoring them for timely closure.
- Help coordinate compliance training by organizing cGMP sessions for staff, updating training matrices, and ensuring all employee training records are current and audit-ready.
- Assist during internal and regulatory audits by promptly retrieving requested batch records, preparing compliance evidence, and supporting senior QA members in daily facility walkthroughs.
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Section · 02
Skills
Quality Manualscompliance evidenceinternal and regulatory auditslogging deviationsQMS DocumentationStandard Operating Procedureschange controlsTraining matricescapasGITBatch records
Section · Company
About USV
USV
Pharma
7.1k+
employees
1961
65 years old
Mumbai, Maharashtra
India
About
USV India is the top old leading healthcare industry & pharmaceutical company in Mumbai, India. They provide API, Peptides, Biosimilars, Injectables, Ophthalmics & Solid Orals products in India
Industries
PharmaManufacturing
Employee ratings
1,753 reviews
4.0/ 5
Culture
3.8
Career growth
3.5
Work-life
3.8
Employees rate it well for
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