Description
This role is a very exciting position for someone looking to move to a company based in the North West that is growing rapidly in to the Medical Device market and be involved in the role out of new and existing products in to new markets.The role will involve;
- Liaising with commercial and QA teams and advising on regulatory strategy.
- Providing medical device expertise to the already successful team to ensure smooth and quick roll out of new and existing products.
- Being hands on with regulatory functions such as Technical files, Product submissions, customer and supplier audits and interacting with notified bodies.
- Communicating with the product development team in theUSAto advise on local regulatory and quality requirements.
Required skills;
- Strong hands on medical devices back ground in a regulatory capacity.
- Working understanding of quality assurance, quality management systems, or QA management.
- Proven delivery of strategic regulatory & quality procedure
- Experience in Sterilisation, wound care, or infection control would be beneficial but not essential.
- Strong communication skills, product leadership, and good commercial understanding are all highly desirable for this role.
- Experience of working in the EU,USAend emerging markets would be desired.
My client is looking to pay Circa £55,000 for this role and looking to move quickly, I have interview slots available and I am currently short listing candidates so if you believe you have the correct experience for the role then please send me your CV and I will be in touch shortly.
To find out more about Real please visit www.realstaffing.com