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Managing Consultant @ Cpl Life Sciences | Life Sciences Specialist /Regulatory Affairs & Quality
Job Title: Regulatory Affairs Specialist/Consultant – Self Care
Job Type: 6-monthcontract, likelihood of going permanent (Inside IR35)
Location: High Wycombe, UK – 2x a week in the office
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 the self-care (Medicines, food supplements, cosmetics) portfolio.
Responsibilities:
* Regulatory review and approval of product labelling for Medicines, food supplements, cosmetics classes per the company portfolio in mainly UK & EU and EMEA
* Assists in the preparation of dossiers and submission packages for the registration and maintenance of products
* Participate in the development and implementation of, and maintain compliance with, all applicable Processes, SOPs
* Regulatory review and approval and advertising or promotional copy
* 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 approval
* Complete market impact assessments
Experience/Qualifications:
* Minimum B.S. Chemistry, Biology, or related fields
* Significant experience in Consumer Health/ Personal care Regulatory affairs mainly with new registrations, 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
* 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 lucy.kirkaldy@cpl.com
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Science and Quality Assurance
* Industries
Personal Care Product Manufacturing, Consumer Services, and Pharmaceutical Manufacturing
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