Job Overview
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Date PostedDecember 1, 2022
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Location (State / UT)
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Expiration date--
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Experience6 Years, 12 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
Drive compliance of unit as per Quality management system and regulatory expectation while seeking continuous improvement in cGMP to ensure
Key Accountabilities
- Establish a system for appropriate investigations of various non-conformances of quality management systems, to determine the root cause and implementation of CAPA, as per cGMP requirements
- Design plan for compilation, review, and on-time closure of QMS documents in order to meet compliance with respective quality systems
- Control the system to analyze QMS documents for completeness and accuracy in line with cGMP requirements
- Seek opportunities for continual improvements in QMS by review of regulatory updates through simplification of SOPs/procedures to ensure adherence to cGMP requirements
- Plan regulatory compliance of audit observations by monitoring and supervising compliance till its closure to meet regulatory compliance
- Direct and supervise communication to provide feedback to internal and external customers on queries related to QMS documents/deficiencies as per standard procedures and technical agreements
- Developed them in performing their job roles better and contributing to achieving team goals
Education Qualification
B. Pharm. / M. Pharm. / M. Sc
Relevant Work Experience
8-12 years for B. Pharm or 6-8 years for M. Pharma / M. Sc.