Hello,
Covalence Pharma is looking for a Regulatory Affairs Specialist based in the EU! We will be at the Euro Convergence in Brussels and would love to meet and discuss. The position will start as remote with a transition to hybrid in the future A full job description will be posted on the RAPS job board, but the position summary is as follows:
Reporting to the Director of Regulatory Affairs, the Associate/Senior Regulatory Affairs Specialist EU/UK is responsible for ensuring that products comply with regulatory requirements, typically for pharmaceuticals, medical devices, or food products. The Associate/Senior RA Specialist EU/UK will understand implementation of the drug development process in a regulated environment, including topics such as Quality by Design (QbD), Design of Experiment (DOE), and compliance with ICH and regional regulatory guidelines. The Associate Senior RA Specialist will prepare and submit regulatory documentation, maintain compliance records, and liaise with regulatory agencies. The Associate/Senior RA Specialist EU/UK will be involved in strategic planning, team leadership, and direct communication with regulatory authorities as well as supporting global regulatory activities within Covalence Pharma.
If interested, please forward your resume/CV or reach out with any questions to deema@covalencepharma.com or me (lisa@covalencepharma.com).
Kind regards,
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Lisa Apolis, RAC
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