2 weeks ago

Regulatory Coordinator

Stoke Stoke-on-Trent Competitive Permanent

Regulatory Coordinator

The opportunity to work within a well-established and pioneering provider of medical device products. You will work within a close-knit and collaborative team within a growing company with great progression potential.

Working within the regulatory affairs team, this fast-paced opportunity gives you the chance to be a part of a growing business and to make a genuine contribution to their future.

This job role could suit a fresh graduate with a relevant BSc degree and the desire to develop a career in regulatory affairs.



The position:

The key focus of this role is to support regulatory obligations of the organisation and its products throughout the full product lifecycle. Preparation and submission of documents for registering and maintaining the Company’s site and global product registrations in accordance with specified country requirements. Coordinating information systems to track registration status and renewal dates for products and regulatory documents.

Experience:

  • Relevant BSc degree in a Life Science subject
  • Some previous experience with medical devices is an advantage but not essential
  • Previous knowledge of regulatory affairs (from university module or training course) would be a benefit
  • Strong organisational skills
  • Ability to accurately follow written instructions
  • Proficient with Microsoft Office packages
  • Brilliant communication skills and enthusiasm towards work
  • Must be willing to work in office Monday-Friday 9am-5pm

Key Words:

Regulatory affairs, RA, documentation, physical testing, test, inspection, protocols, procedures, ISO 13485, medical device, meddev, medical technology, audit, SOP, graduate, entry level, junior, trainee, training, progression.

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