Regulatory Affairs Specialist/Consultant – Cosmetics

Details of the offer

Job Title: Regulatory Affairs Specialist/Consultant – Cosmetics Job Type: 6-month contract (Inside IR35) Location: Buckinghamshire, UK – 2x a week in office Pay Rate: £65ph - £70ph We are partnered with a leading Consumer Health organization who are looking for an experienced Regulatory Consultant to join on a 6-month contract basis.
This role will be dedicated to cosmetics and a non-OTC portfolio.
Responsibilities: Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly UK & Ireland Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC classes mainly in UK & Ireland Support the Regulatory team with specific tasks per the needs of the department, which may include claims tracker updates, databases, compliance tasks Work with the regulatory team to develop project implementation plans and manage resource planning to ensure on time completion of projects and tasks Project management and implementation of regulatory changes to company assets (product label and promotional materials) Work with cross-functional partners to drive regulatory strategy and implementation Regulatory review and approval of key documents before product ap Complete market impact assessments Portfolio survey (where used of ingredients) Experience/Qualifications: Minimum B.S.
Chemistry, Biology, or related fields Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing multiple brands.
Well-versed with UK ASA, CAP, BCAP Guidance for Advertising, proven record of successful project management of dossiers with ClearCast Strong knowledge and application of the UK & EU Cosmetic Product Regulation Excellent leadership, communication, and organizational skills Attention to detail, effective in written and oral communication Works independently to plan, conduct, and manage regulatory projects to meet department and company objectives Responsible for identifying, implementing and managing key RA Departmental projects and/or strategies based on both short- and long-term RA Department objectives.
You must be able to be based on site 2x a week in Buckinghamshire, UK, and have the FULL right to work in the UK.
For more information or to apply please reach out to ******


Nominal Salary: To be agreed

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