Quality Assurance Role - Pharma/Medical Equipment (3-5 yrs)
Job Highlights :
- Responsible for review and documentation related to OOS,Non-Conformity,Deviation,CAPA,and Change Control & updation of all QA Logbooks (Batch issuance,DCR,NDR,NCR,CAPA etc.)
- Should have good computer knowledge and communication skills
- EU MDR, ISO 13485, Pharma, He will be maintained QMS documentation & validation as per MDR 2017, WHO guidelines
Posted on Jun 14 2021
Job Description :
- The candidate should be maintained QMS documentation & validation as per MDR 2017, EU MDR, ISO 13485, WHO guidelines.
- Responsible for review of Site Master file, Quality Manual, Technical File.
- Responsible for document control, review, issue, retrieval & superseding of all SOP related to Manufacturing, Engineering. Warehouse, HR, Plastic section, Quality Control, QA and Purchase Departments respectively and updating of Master Document Index for QA and all other departments
- Responsible for review and documentation related to OOS, Non-Conformity, Deviation, CAPA, and Change Control & updation of all QA Logbooks (Batch issuance, DCR, NDR, NCR, CAPA etc.)
- Should have good computer knowledge and communication skills
Industry Type : Pharmaceutical & Life Sciences
Functional Area : Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role : Bio/Pharma Informatics-Associate/Scientist
Employment Type : Full Time, Permanent
Education :
B.Pharma in Any Specialization, B.Sc in Any Specialization
This job opening was posted long time back. It may not be active. Nor was it removed by the recruiter. Please use your discretion.
