Regulatory Specialist and Senior Specialist

1 month ago

Buckinghamshire, United Kingdom Cpl Life Sciences Full time

Job Title: Regulatory Affairs Specialist Employment type: 6-Month Contract – Outside IR35
Location: Buckinghamshire, UK – 2 days on-site per week.
50 Per Hour via Limited or Umbrella.

An opportunity to join a global leading consumer health business and be responsible for supporting UK and Ireland Cosmetic and non-OTC submissions. The role will require a senior professional to join the business with a wealth of experience in Consumer health care especially within cosmetics and non-OTC products.

This role is a 6-month contract position requiring the right candidate to be based in their Buckinghamshire offices two days per week. Ideally looking for the right candidate to start ASAP.
Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly the UK & Ireland
Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC classes mainly in the 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 labels and promotional materials)
Work with cross-functional partners to drive regulatory strategy and implementation
Regulatory review and approval of key documents before product ap
Portfolio survey (where used of ingredients)

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
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.

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