✨ About The Role
- The Manager will be responsible for managing and executing complex projects in support of clients in the Biomedical Engineering & Sciences Practice.
- This role involves actively participating and providing leadership within the practice while marketing its technical and regulatory capabilities.
- The position requires participation in technical projects related to medical devices, pharma, biologics, and combination products.
- The Manager will direct regulatory strategy assessments and technical evaluations for multinational medical device companies.
- Expanding expertise through peer-reviewed publications and developing the careers of support staff is also a key responsibility.
âš¡ Requirements
- A Ph.D. in Bioengineering, Biomedical Engineering, Materials Science, or a related field is essential for this role.
- Candidates should have at least 5 years of post-Ph.D. professional experience, particularly in the life sciences industry.
- Experience with software as a medical device and familiarity with medical device regulatory requirements is crucial.
- Strong leadership skills and the ability to manage and develop a team of professionals are necessary for success.
- Excellent verbal and written communication skills are required to convey complex technical issues to non-technical audiences.