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QA Manager - Medical Devices

Up to £40k DOE | Yorkshire & The Humber |  Quality Assurance and Supply Chain, QA |  Contract  | Ref:889736

The Role

QA Manager - Medical Devices - Sheffield - 6 Month FTC - Up to £40k DOE

 

The Company

A highly dynamic and growing medical devices company that specialise in developing and manufacturing prosthetics across the UK, Europe and the US. With this role they are offering:

  • Generous salary for 6month FTC
  • Opportunity to travel nationally and internationally
  • Work closely with the Quality, Engineering and Continuous Improvement teams
  • Exposure to an exciting sector within the medical devices market

 

The Role

Our client is looking for an experienced QA Manager to support their R&D, Engineering and Manufacturing functions at their Sheffield site on a 6month FTC. General responsibilities include:

  • Ensuring compliance within the MDR directive, ISO 13485/9001 and FDA 21 CFR Part 820
  • Leading internal and external audits
  • Supporting Engineering and R&D teams to ensure product consistency and compliance
  • Implementation, maintenance and training on QMS activities
  • Promoting company awareness of the Quality Policy, Objectives, Procedures

 

You

  • Have experience within QA and QC in a highly regulated environment; medical devices, engineering, aerospace, tech manufacturing etc
  • Good knowledge of ISO and MDR regulations
  • Experienced leading internal and external audits
  • Have the ability to travel on occasion if necessary to the business
  • Be available immediately or have a short notice period

 

What should you do next?

This QA Manager role is one not to be missed; it encompasses the opportunity to niche product pipeline in an exciting medical devices business! To discuss further, please submit your current CV.

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

Consultant

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Nadya Libecans

Which team and area do you work/specialise in?

I work on the Drug Development team specialising in Quality (QA) and Supply Chain roles within the pharmaceutical, medical devices and consumer healthcare markets.

What are some of the typical roles you cover?

I cover all levels from Administration to Director level within QA, QC, Supply Chain, Procurement and Logistics.

What are the hot issues in your sector currently?

For both Quality and Supply Chain, Brexit is a huge topic at the moment. Clients and candidates I work with have been working extensively to organise contingency strategies to minimise the effects to cost of manufacture and speed of product delivery.

What’s makes you #DistinctlyDifferent?

I believe knowledge is power and I strive to learn as much about people and the industry as possible to build lasting relationships and produce the best results for candidates and clients. 

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