Global Regulatory Associate Post Approval Maintenance - Medical Devices

Kingston upon Hull, ENGLAND | 12 days

Job Summary


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Job Description


Role Summary:
 
Would you like to work on some of the most well used medical device products found in homes all over the world? Our team looks after medical devices from Scholl, Optrex as well as many other brands. We are looking for someone with a passion for medical devices to join us to maintain compliance of our portfolio globally post launch.
 
With experience of working with medical device products in an R&D, quality or regulatory setting you will provide technical expertise to deliver complex projects including ingredient reformulation programs. With strong attention to detail you will be a technical expert who will work with other regulatory groups and business stakeholder functions to maintain regulatory compliance of our products across the world.

 


Essentials

  • Life Science or Chemistry degree, or equivalent

  • Minimum 2 years’ experience of working with medical devices in either a regulatory, quality or R&D setting

  • Understanding of EU medical device landscape

  • A self-starter you are results orientated and have a collaborative approach

  • Proven ability to manage numerous projects to deliver on time

  • Strong communication skills

 

Desirables


  • Experience in ingredient removal programmes in cosmetic products

  • Experience of collation of dossiers and data packages

  • Understanding of global medical device regulations

 


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