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RA/QA Specialist

Hays Specialist Recruitment Limited
Posted 7 hours ago, valid for a day
Location

Uxbridge, Buckinghamshire UB8 1DH, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

info
  • The company is a growing medical device firm focused on product development, manufacturing, and distribution across various healthcare sectors.
  • The role involves supporting quality assurance and regulatory affairs, ensuring compliance with UKCA, EU MDR, and FDA regulations.
  • Candidates should have experience in the medical device field, ideally with knowledge of ISO13485, and a relevant science-based degree.
  • The position requires excellent report writing skills, attention to detail, and strong organizational abilities, with a salary of £40,000 to £50,000.
  • A minimum of 3 years of experience in the medical device industry is required for this role.

Your new companyOur clients are a growing medical device company specialising in product development, commercialisation, manufacturing, sales and distribution. The product range includes IV therapy, diabetes care, surgical, anaesthesia, sexual health, cosmetics, etc. With a strong presence across the UK and Europe, they are committed to delivering high-quality, innovative healthcare solutions that improve patient outcomes. Your new roleYou will support with all quality assurance and regulatory affairs activities - ensuring the company's policies are implemented as part of normal processes across the company.You will be involved in:

  • Liaising with stakeholders to ensure they maintain compliance with the company's policies and procedures.
  • Supporting company's Quality Management System (QMS)
  • Compliance with UKCA, EU MDR, FDA
  • Writing, reviewing, and maintaining technical files as well as other relevant regulatory documentation (e.g. MDD, UKCA, MDR, IVDR, Procedure pack)
  • Product development
  • Keep up with relevant regulations or (ISO) standards updates
  • Ensuring that the business is working towards a smooth MDR implementation/transition process.
  • Coordinate both internal and external audits.
  • Ensuring compliance is always kept to the highest standard.
  • Document control - updating quality procedure documents and product fact sheets to make sure they are accurate.

What you'll need to succeed

  • Experience within the medical device field, all classes of medical devices
  • Good general knowledge of ISO13485 is preferable.
  • Relevant science-based degree
  • Logical thinking and proactive approach to problem-solving.
  • Good interpersonal skills.
  • Excellent report writing skills with a strong attention to detail.
  • Good organisational and time management skills, with the ability to prioritise and handle a complex, varied workload.
  • Office software: Microsoft, Adobe, etc.
  • Multi-language skill is an extra

What you need to do nowIf you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.