PE Global are currently recruiting for a Senior Regulatory Affairs Specialist with experience in Cosmetics and/or Medical Devices for a 5 month contract role with a leading multinational Consumer Health client based in Reading (hybrid).

Responsibilities

• The Senior Regulatory Affairs Specialist has an in-depth understanding of the regulatory environment within their geographical area of responsibility as well as requirements for regulatory submissions, approval pathways and compliance activities and the potential impact of these on business objectives.
• Ensures the success of new product registrations, line extensions and new indications and claims in alignment with the business plan
• Manages the coordination, compilation, submission of new drug applications, cosmetics, medical devices, food supplements or any similar product to the regulatory agencies within their geographical and/or brand area of responsibility
• Maintains compliance for all products with local regulations and quality system requirements

Requirements

• An early start date is required. Ideally, candidates should have a notice period of no more than one month
• Relevant Bachelor's Degree or higher
• 6+yrs related regulatory experience
• Expertise across a broad spectrum of Regulatory classifications including Medicinal Products, Cosmetics, Commodities and/or Medical Devices
• Knowledge of regulatory frameworks and external environments, and the ability to apply these to regulatory solutions throughout the product lifecycle.
• Solid understanding of regulatory/medical/safety/quality requirements in the markets of relevance.

Interested candidates should submit an updated CV.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***