Regulatory Affairs Specialist - Buckinghamshire, United Kingdom - Cpl Life Sciences

Description

Job Description

Job Title: Regulatory Affairs Specialist

Employment type: 6-Month Contract – Outside IR35

Location: Buckinghamshire, UK – 2 days on-site per week.

Rate: £84.50 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.

Responsibilities and Deliverables:

• 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
• 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.

Please note this role does not offer sponsorship and needs the right candidate to be based around Buckinghamshire.

For more information please contact