- responsibility for post-approval activities including, variations (type 1a, 1b, and type 2), renewals, license changes, and CMC change controls.
- of new MAA in the UK and Europe and support with any new registration applications.
- understanding of MA transfers.
- labelling and artwork changes (SmPc, PIL, and mock-ups)
- submission, and management of approvals of National, MRP, DCP, and CP applications in the UK and European region.
- degree or higher in Life Sciences or technical field.
- years of relevant regulatory experience.
- strong communicator who is able to navigate through difficult conversations with senior stakeholders.
- EU market experience with strong experience submitting through MRP, DCP and national procedures.
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Senior Regulatory Affairs Officer - London, United Kingdom - Cpl Life Sciences
Description
Job Title: Senior Regulatory Affairs Officer
Employment Type: Permanent
Location: East London, 3 days on-site per week. (Hybrid)
Salary: Up to £50,000
Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical company that specialising in medicinal, non-medicinal, medical devices, and OTC products. The business is increasingly growing and is looking for a personable and detail-oriented professional to join the team.
As a Senior Regulatory Affairs Officer, you will be responsible for managing regulatory submissions in the UK and European markets including supporting over 150 product licenses. In the role, you will be supporting MA transfers, new MAAs, Variations, and renewals.
Responsibilities
Requirements
This position allows for great career progression opportunities as well as the chance to work for a growing organisation. The role includes some excellent benefits and will be an excellent opportunity for a junior RA professional.
To apply for this role you must have the full right to work in the UK as this employer does not provide sponsorship. For more information please contact