Regulatory Affairs Specialist

Up to £56 per hour LTD
04 Jun 2021
04 Jul 2021
Lucy Stendall
Regulatory Affairs
Full Time
Contract Type
Experience Level
Experienced (non-manager)
CK Group are recruiting for a Regulatory Affairs Specialist to join a company in the Pharmaceutical industry at their site based in Maidenhead on a contract basis for 6 months.

Hourly Up to £56 LTD

Regulatory Affairs Specialist Role:
• Management of a product or specified products within a therapy area for Cosmetics, OTC and/or Medical Devices
• Development of regulatory strategies, preparation of regulatory applications and support maintenance activities within relevant therapy area
• Responsible for regulatory activities related to National and/or European procedures (Decentralised, Mutual Recognition) as appropriate.
• Define regulatory strategies (local and regional) in line with business plan.
• Complete identified regulatory activities to ensure all regulatory obligations and business objectives are met.

Your Background:
• Life sciences or chemistry graduate to honours level or equivalent.
• Must have UK market regulatory experience within pharmaceutical regulatory affairs and working with MHRA directly, ideally with some OTC experience
• Brexit related regulatory knowledge and experience
• Must have hands on experience in management of day to day UK and EU regulatory procedures
• Ideally knowledge and experience of allied regulatory affairs areas such as Cosmetic, Medical Devices but not essential

Our client is part of one of the largest Pharmaceutical companies in the world. Their Consumer segment includes a broad range of products used in the baby care, skin care, oral care, wound care and women's health care fields.

This Regulatory Affairs Specialist role will be based at our clients site in Maidenhead, Berkshire.

Entitlement to work in the UK is essential. Please quote reference 50799.

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