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Regulatory Affairs Contractor - Pharmaceuticals - 6-Month Contract
Our client has an exciting new opportunity for a regulatory affairs contractor to join the team. They have specialized in pharmaceutical products and people's well-being for over a century, working with some well-known household brands.
Responsibilities:
* Principle responsibilities will be within Consumer Health OTC medicines but may also include assisting in regulatory support for other product types such as Cosmetics, Medical Devices, and Food Supplements.
* Development of regulatory strategies, preparation of regulatory applications, and support maintenance activities within relevant therapy areas.
* Support the team with regulatory activities for National and/or European procedures (Decentralised, Mutual Recognition) as appropriate.
* Maintain awareness and knowledge of current regulatory legislation.
* May act as an ambassador for the Regulatory Affairs department to raise the profile of the team both internally and externally.
Requirements:
* Life sciences or chemistry graduate to honours level or equivalent.
* Work with minimal supervision to plan, conduct, and manage regulatory submissions and multiple projects to meet department and company objectives.
* Determine and develop approaches to solutions with technical guidance on problems of moderate scope and complexity.
* May mentor Graduate and Regulatory Executive staff and provide day-to-day support as appropriate.
* Experience in project management, understanding of the regulatory environment, interaction with Regulatory Authorities (as appropriate), commercial/strategic awareness, implementing regulatory strategies, managing and maintaining Marketing Authorisations.
Hybrid work model: 1-2 days in the office per week.
If this role interests you, please apply now!
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