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Job Location | Glasgow |
Education | Not Mentioned |
Salary | Competitive salary |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent , full-time |
Production Manager, ProjectsAn exciting opportunity for an experienced scientific production manager to work at a Glasgow based CDMO overseeing the manufacture of pharmaceuticals products. If you have cGMP line management experience in pharmaceutical or scientific manufacturing, aquality focused approach and a flair for problem solving, then we would love to hear from you. Lead and be part of a dynamic and friendly team. A highly competitive salary and benefits package are on offer in addition to an excellent work culture, which fosterscollaboration and support.The Role This role based in the Glasgow GMP production team is responsible for oversight of the technical delivery of the Glasgow production project leaders team. This role is critical in supporting the delivery of GMP manufacturing projects to agreed timelinesand budget.The post-holder will work directly with client representatives, generating batch manufacturing process documentation, overseeing delivery of manufacturing projects and completion of documentation for QA review.The post-holder will provide data for KPIs management and ensure delivery to required standards and timelines are achieved.The post-holder will be a department Subject Matter Expert who will have responsibility for final department sign off on Quality events, change control and CAPA.ContextThis role operates in a heavily regulated industry and GMP environment and duties are required to be carried out in compliance with all relevant internal procedures, GMP and customer specific documentation.The role reports to the Operations and Supply Chain Manager, Production and works collaboratively across site senior managers in Formulation Development, Project Management, Quality and Facilities/Engineering to ensure efficient execution of suitably robust,compliant and safe processes aligned with client product specifications and EU GMP standards.A collaborative approach with key production team members will be required.ResponsibilitiesThe post holder is responsible for ensuring: