Regulatory Specialist – South Wales – £40-50k
The Regulatory Affairs Leader provides subject matter expertise and works with a team of regulatory affairs professionals to ensure the company establishes best practice within the assigned area of responsibility (regional regulatory submissions reporting, technical standards, collection and dissemination of intelligence, influencing the global regulatory environment, etc).
1. Bachelor's Degree or equivalent with a substantial level of experience in the medical device or pharmaceutical industry or government / government relations; OR a vast level of progressive regulatory affairs experience in medical device or pharmaceutical industry or government / government relations, including knowledge experience applying global drug or device laws regulations for product registration, adverse event reporting, recalls.
2. Ability to prioritize, plan evaluate deliverables to established strategic goals.
3. Demonstrated experience operating in a highly regulated environment; Proven application of analytical skills in a regulatory environment
4. Demonstrated knowledge experience conducting scientific, regulatory, legal, or business research.
5. Excellent verbal, written communication and presentation skills with the ability to communicate business issues in English Language with an easy to understand manner
6. Prior experience using spreadsheet and presentation software
7. Must be willing to travel up to 15% of time.