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Quality Manager

Adecco
Posted 22 days ago, valid for 11 days
Location

Plymouth, Devon PL4 6DX, England

Salary

£50,000 - £60,000 per annum

Contract type

Full Time

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Sonic Summary

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  • Job Title: Quality Manager
  • Location: Plymouth
  • Salary: Not specified
  • Experience Required: Bachelor's degree or 4+ years in medical device or pharmaceutical industries
  • Responsibilities include providing leadership, managing Quality Strategy, ensuring compliance with regulations, managing budgets, overseeing new product development, and making quality-related decisions.

Job Title: Quality Manager

Location: Plymouth

Our client, a leading medical device company, is seeking a dynamic and experienced Quality Manager to join their team. As the Quality Manager, you will play a vital role in ensuring the delivery of the Quality Strategy and driving continuous improvements.

If you are passionate about quality and have a strong background in the medical device industry, we want to hear from you!

Responsibilities:

  • Provide leadership to the site quality function, including quality systems, quality engineering, and QC analytical and Microbiology.
  • Manage the successful delivery of the Quality Strategy to achieve corporate goals and objectives.
  • Ensure compliance with MDSAP regulations, and the Medical Device regulation (MDR).
  • Prepare and manage the budget for the site quality function.
  • Ensure effective delivery of new product development by overseeing quality deliverables and compliance with design control and validation requirements.
  • Make decisions related to quality issues, conduct root cause analysis, and implement corrective actions to avoid product recalls.
  • Review and approve supplier and customer quality agreements to meet compliance and operational requirements.

Requirements:

  • Bachelor's degree or equivalent in a scientific discipline or 4+ years of experience in the medical device or pharmaceutical industries.
  • Demonstrated leadership experience in previous roles.
  • Proficient knowledge of applicable Quality System Regulations and ISO quality requirements.
  • Familiarity with the Medical Device regulation.
  • Strong knowledge of QA, Manufacturing, Validation, Change Control, and Design Control processes.
  • Proficiency in spreadsheets and word processor applications.
  • Solid understanding of statistical methods, sampling plans, and statistical analysis.
  • Experience with analytical methods, equipment, process, software, cleaning, and/or facility/utility validations.

If you're interested to know more, please get in touch!


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