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Medical Device Project Manager

Job LocationMildenhall, Bury St. Edmunds
EducationNot Mentioned
Salary40,000 - 42,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent,full-timeP

Job Description

Medical Device Project ManagerMildenhall, Suffolk (Re-location package available depending on location)£40,000 - £42,000 + benefits.Offering excellent, long term progression and exceptional on-the-job trainingOur client a successful & well-established medical device manufacturer are looking for a Project Manager to join their ever-expanding team, to take a project lead in bringing medical projects from concept/design stage through regulatory approvals and ontosale. The company design & manufacture medical devices ranging from Class 1 through to Class III. Theyre used within a wide range of interesting and challenging medical fields. The company has been synonymous with world-class products and innovation and haveshown repeatedly why theyre the company to lead product development for the Biomedical industry.The experienced project leader will oversee the design and development of new and innovative medical devices. Ideal candidates must have previous experience in project leading full-lifecycle medical device product development e.g. from concept, through designand development, clinical trial, regulatory approval, manufacture and product launch.Some of the key responsibilities of the job role will include:

  • Working closely with the stake holders to gather relevant concept information.
  • To facilitate in the concept and design of products that meet the projects needs.
  • To provide project leadership that includes management of budget, timeline and resources.
  • Generation of project documentation in line with ISO 13485 and other medical device regulatory requirements.
  • Generation of regular project update reports
  • Attend and organise regular project meetings.
  • To engage relevant vendors and subcontractors to support the needs of the project.
  • To develop product test methods, data analysis and evaluations to determine or prove product performance and reliability.
  • To function within all quality systems and regulations, particularly related to medical devices.
  • Global and UK travel will be required to satisfy the needs of the project.
  • Support in the design, concept and development of product manufacturing equipment.
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