Production Scheduler – Medical Devices
Salary: £40,000 to £45,000 per year.
Location: Abingdon, Oxfordshire (commutable from Oxford, Abingdon, Didcot, Dorchester, Aylesbury, Bicester, Witney, Shrivenham).
We are a rapidly growing, innovative medical device engineering company focused on product development and low‑volume manufacturing. Our brand‑new office and clean‑room production facilities provide a dynamic environment for a newly created Scheduler/Coordinator role that plans and coordinates multiple concurrent production projects.
Key Responsibilities
- Plan, coordinate, and monitor production activities across multiple concurrent projects within a small‑scale medical device manufacturing environment.
- Ensure efficient allocation of resources, timely delivery of products, and alignment with ISO13485 requirements.
- Act as the key interface between manufacturing, supply chain, quality, and engineering to ensure production plans are realistic, controlled, and executed in compliance with medical device regulatory and quality standards.
Qualifications and Experience
- Experience in a Production Scheduler, Production Coordinator, Project Coordinator, Operations Coordinator, or similar role within a medical device manufacturing environment.
- Strong organisational skills with the ability to manage multiple priorities.
- Knowledge of ISO13485, GLP/GMP preferred; experience in low‑volume, R&D or design‑development manufacturing processes.
Production Scheduler – Medical Devices
Salary: £40,000 to £45,000 per year.
Location: Abingdon, Oxfordshire (commutable from Oxford, Abingdon, Didcot, Dorchester, Aylesbury, Bicester, Witney, Shrivenham).
We are a rapidly growing, innovative medical device engineering company focused on product development and low‑volume manufacturing. Our brand‑new office and clean‑room production facilities provide a dynamic environment for a newly created Scheduler/Coordinator role that plans and coordinates multiple concurrent production projects.
Key Responsibilities
- Plan, coordinate, and monitor production activities across multiple concurrent projects within a small‑scale medical device manufacturing environment.
- Ensure efficient allocation of resources, timely delivery of products, and alignment with ISO13485 requirements.
- Act as the key interface between manufacturing, supply chain, quality, and engineering to ensure production plans are realistic, controlled, and executed in compliance with medical device regulatory and quality standards.
Qualifications and Experience
- Experience in a Production Scheduler, Production Coordinator, Project Coordinator, Operations Coordinator, or similar role within a medical device manufacturing environment.
- Strong organisational skills with the ability to manage multiple priorities.
- Knowledge of ISO13485, GLP/GMP preferred; experience in low‑volume, R&D or design‑development manufacturing processes.
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