Cencora is looking for a Senior Manager, Medical Devices to lead and deliver regulatory and quality client projects across medical devices, in vitro diagnostics (IVD), and combination products.
Requirements
University degree in Science, Medicine, Law, Engineering, or a related discipline.
Significant, hands-on experience in medical device and diagnostics (including IVD) regulatory affairs and quality management.
Strong analytical and critical-thinking skills, with a track record of resolving complex issues independently and pragmatically.
Proven project management capability (planning, execution, risk/issue management, and delivery to timelines and quality standards); experience driving change management initiatives is desirable.
Strong stakeholder management up to client department-head level; excellent written and verbal communication and presentation skills.
Business-fluent English and local language.
Companion Diagnostics (CDx) and/or combination products (desired) Benefits
Competitive compensation and benefits package
Senior, highly visible role focused on meaningful client delivery in the medtech space
Collaborative, expert-led environment where you can share knowledge, influence best practice, and drive continuous improvement
Professional development opportunities to further deepen your regulatory/quality expertise and leadership capabilities
