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| Job Location | Vadodara |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | Sales / BD |
| EmploymentType | Full-time |
Roles and ResponsibilitiesFor R&D and Contract Research Labs and Manufacturing. Working for UK, EU Market.You will be responsible for,1. Review and approve process and analytical method transfers.2. Lead timely discussion of OOS with other Technical Managers and plan appropriate timelyface to face or telecon discussion with all stakeholders.3. Manage the Quality aspects of several Contract Manufacturing Organizations.4. Provide onsite Quality support for product transfers.Desired Candidate ProfileCandidate should be B. Pharma / M. Pharm / M. Sc with 10 years experience in working in apharma company. Proven experience of Manufacturing, API, solid dosage forms, liquids, creamsand sterile products.1. knowledge of Current Good Manufacturing Practice, Standard Operating Procedures, EUGMDP guidelines, regulations and ICH Guidelines.2. Experience of working in a Quality Department of a pharmaceutical.3. Experience in Contract Manufacturing audits and Third-Party Audits.4. Experience in Quality Systems, Quality Operations, QC Laboratory, Analytical orProcess Validation, Manufacturing, Production or Warehouse.,
Keyskills :
contract manufacturingproject managementpharmaagilestandard operating proceduresjavacontinuous improvement facilitationoperationsapiquality operationscustomer relationsdeliveryresearchoosquality systemsichforms