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Associate Regulatory Affairs Manager, Consumer-Northern Europe

Berkshire   •  £60 - £70 per hour  •  Contract/Temporary, Full time

My client, a large and highly successful pharmaceutical client is looking for an Associate Regulatory Affairs Manager on an initial 3 month contract. There will be flexibile home working on offer.


Develop and support regulatory strategies in line with business plan

Partner with brand and cross functional team to explore new and revised claims for advertising copy and pack that are within the frameowrk on the product classification

complete regulatoy activities for a defined number of products to ensure all regulatory obligations and business objectives are met

Sign off packaging material, leaflets, and adveritising/promotional material to ensure regulatory complaince for submissions via appropritate document approval systems

Assist Crisis Management/PR Matters as related to regulatory affairs

Fulfil Department complaince obligations that include:

Processes, SOPs, working instructions adherence and ownership of processes for continuous improvement

Update relevant local and global databases to track current product information and facilitate product notification under the Cosmetics Regulation

Support audies and inspections as they relate to Cosmetics

Provide regulatory advice and perform due diligence for product acquisitions and agreements with third parties

Maintain strong awareness/knowledge of current regulatory requirements

Represent Regulatory Affairson cross functional product/project teams and provides regulatory advcie and/or support (as appropriate) both internally and externally. Provide regulatory guidance to internal stakeholders, to allow them to make to key decisions on business-critical activities and project feasibility


Life Sciences, Chemistry degree or equivalent

Sound working knowledge and experience of EU Cosmetics Regulation and associated UK requirements

Good grasp of the regulatory framework and borderline between Medicines, Cosmetics and Medical Devices

An awareness and some working knowledge of Adveritising copy approval requirements in the UK for example. CAP, BCAP and Advertising Standards Authority

Excellent leadership, communication and organisational skills

Detail oriented, effective in written and oral communication

Work 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

If you feel you have a suitable profile and would like to find out more, please apply and get in touch with Ross Wilson at rwilson@keypeople.co.uk for further information.

You must be eligible to work in the UK. Learn more

  • Agency: Key People
  • Reference: 25060
  • Posted: 24th August 2020
  • Expires: 21st September 2020

Key People

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