Regulatory Affairs Contractor - Pharmaceuticals - 6-Month Contract
Our client has an exciting new opportunity for a regulatory affairs contractor to join their team. With over a century of experience in pharmaceutical products and promoting people's well-being, they collaborate with well-known household brands.
Responsibilities:
* Principle responsibilities will focus on Consumer Health OTC medicines but may also include regulatory support for other product types such as Cosmetics, Medical Devices, and Food Supplements.
* Development of regulatory strategies, preparation of regulatory applications, and support for maintenance activities within the relevant therapy area.
* 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.
* Act as an ambassador for the Regulatory Affairs department to enhance the team's profile both internally and externally.
Requirements:
* Life sciences or chemistry graduate to honours level or equivalent.
* Ability to work independently to plan, conduct, and manage regulatory submissions and multiple projects to meet department and company objectives.
* Develop solutions with minimal supervision, guided by technical expertise, on a variety of moderately complex problems.
* Potential to mentor Graduate and Regulatory Executive team members and provide daily support as appropriate.
* Experience in project management, understanding of the regulatory environment, interaction with Regulatory Authorities, strategic awareness, implementation of regulatory strategies, and management of Marketing Authorisations.
Work is hybrid, requiring 1-2 days in the office per week.
If this role interests you, please apply now!
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