Job Overview
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Date PostedOctober 1, 2022
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Location (State / UT)
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Expiration date--
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Experience10 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
Responsibility :
- Manage on-site/desktop audits and evaluate Regional suppliers and Third Party Manufacturers
- Create, maintain and execute Audit Schedules in the Trackwise Audit system and ensure its compliance
- Review Quality Questionnaires returned by the Suppliers/TPMs and resolve any issues.
- Assess the appropriateness and timeliness of proposed CAPAs, and track CAPA follow-up to close for supplier and TPMs audits
- Participate in internal audits of Manufacturing site & affiliates auditing program.
- Review & verify CAPA for observations arising from Regulatory Agency audits & Internal audit observations, at the manufacturing site for its completeness and implementation.
- Manage Affiliate Audit program,
- Support the regional management in the execution of various assigned tasks
Experience & Skills:
- Performing Audits in Drug products – Sterile & Non-sterile, API, Biosimilar products, etc.
- Excellent communication skills & report writing skills in the English language
- Risk analysis, CAPA Development
- Computer skills for Microsoft Presentation / Word Document /Excel & PDF
- 10+ years of experience in Pharma Auditing in an MNC / Large Pharmaceutical Company.