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| Job Location | Newark |
| Education | Not Mentioned |
| Salary | £30,000 - £40,000 per annum, negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Regulatory Affairs and Quality AssuranceSalary up to £35,000NottinghamThe company A health challenger brand who is not afraid to stand out from the crowd. Personal care, along with a good dose of fun, is at the heart of everything that they do.Why would I want to work hereThis is an amazing opportunity to join a business entering another decade of success looking to appoint part of their growth. They are a challenger brand with a passionate and collaborative team at the heart of it. You would be joining at a pivotal point in their journey and could progress extensively with them.ResponsibilitiesYou will manage our cosmetic and medical device QA and certification following the product development with third party manufacturerWorking with our contract manufacturers and our distributors and internal team to take ownership of our regulatory and QA processes to assist in a smooth registration process of our range of products in our key targeted countries.Ensure pack claims can be substantiated and labeling is in accordance with Company, Supplier, International Standards and Customers requirements to ensure complianceAdvise the sale team on how to properly market new products within the remit of relevant regulationsYou will work with the product development team on labelling, substantiating claims and with our external lawyers to ensure sign offPrepare, compile, and submit regulatory documents for the registration of current and new products in all international markets especially within the MENA region.To ensure that as a company per product we have up to date PIF’s and registration packs for our customers to assist in their registrationRequirementsHave a degree / BSc in Life sciences or related area.Regulatory Affairs experience working in a pharmaceutical or medical device company is idealIdeally a minimum of 2 years-experience in Regulatory Affairs within the Medical Device industry (MDR) and Cosmetics Required skills
Keyskills :
Health Pharmaceutical Product Development Regulaty Affairs MENA