- Degree in a scientific field with a robust understanding of global regulatory environments impacting consumer products.
- Experience in dossier creation, submission, and product lifecycle management.
- A track record of reviewing and authoring high-quality documents.
- Ability to deliver consistently under pressure, adhering to cost, time, and quality standards.
- Familiarity with the regulatory requirements for medical devices in the EU (MDR) and US (510k) would be beneficial.
- Commercially aware, adept at building partnerships and proposing improvements to enhance business processes.
- Capable of embracing change and setting clear objectives in line with our business goals.