Posted:1 day ago|
Platform:
Work from Office
Full Time
Handling and monitoring of Quality system monitoring, HACCP Activity, cGMP implementation,
Audit & Compliance, Analytical QA, Vendor management, Qualification & Validation, Artwork, Recall, Training, IPQA and Document Management systems.
Oversee QA documentation, QMS events, and GMP compliance.
Manage deviations, CAPA, complaints, OOS/OOT, and APQR.Approve batch records, specifications, validations, and analytical reports.Lead vendor audits, technical agreements, and audit readiness.Drive training programs on GMP/GDP/GLP and quality systems.Preferred Profile:Experience: 818 years in API Quality Assurance.Education: MSc in Chemistry/relatedProven track record in HACCP, cGMP implementation, analytical QA, vendor management, validation, recalls, training, and documentation systems.Location: Hosur, Tamil Nadu
Bioplus Life Sciences
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