Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!
We’re Hiring: Senior Manager, Medical Devices
The Role
We are 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. In this role, you will manage key client relationships, represent clients in interactions with Health Authorities and/or Notified Bodies, and ensure projects are delivered to agreed KPIs, timelines, and budget.
This position is fully dedicated to client delivery and does not include business development responsibilities.
What you'll be doing:
Key Responsibilities
Prepare, review, and compile high-qualityregulatory and quality documentationto support medtech projects.
Provide day-to-day operational support and consultancy to clients onmedtech intelligence, evolving requirements, and best practices.
Develop and maintain strong client relationships; act as thesenior point of contactfor delivery-related matters.
Participate inregulatory, technical, and quality management processesfor pharmaceutical, medical device, and diagnostic clients.
Communicate with clients andHealth Authorities/Notified Bodies; support scientific advice procedures and represent clients in authority interactions as required.
Deliver seminars/lectures for colleagues, clients, and professional audiences; contribute to departmental expertise and knowledge-sharing.
Support company strategy implementation andcontinuous improvement; comply with and help optimise internal processes.
What you'll have:
Qualifications / Skills
University degree inScience, Medicine, Law, Engineering, or a related discipline.
Significant, hands-on experience inmedical device and diagnostics (including IVD)regulatory affairs and quality management.
Stronganalytical and critical-thinkingskills, with a track record of resolving complex issues independently and pragmatically.
Provenproject managementcapability (planning, execution, risk/issue management, and delivery to timelines and quality standards); experience drivingchange managementinitiatives is desirable.
Strongstakeholder managementup to client department-head level; excellentwritten and verbal communicationandpresentationskills.
Business-fluent Englishandlocal language.
Deep subject-matter expertise inCompanion Diagnostics (CDx)andcombined studies(required).
What we offer:
Acompetitive compensation and benefitspackage aligned to experience and location.
A senior, highly visible role focused onmeaningful client deliveryin the medtech space.
The opportunity to work on a broad range ofmedical device, IVD, and combination productprogrammes with leading organisations.
A collaborative, expert-led environment where you canshare knowledge, influence best practice, and drive continuous improvement.
Professional developmentopportunities to further deepen your regulatory/quality expertise and leadership capabilities.
Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.
Full time
Affiliated Companies: PharmaLex Spain S.L.U.
Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.
The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned
On August 30, 2023, AmerisourceBergen became Cencora.
Cencora is a leading global pharmaceutical solutions organization centered on improving the lives of people and animals around the world. We partner with pharmaceutical innovators across the value chain to facilitate and optimize market access to therapies. Care providers depend on us for the secure, reliable delivery of pharmaceuticals, healthcare products, and solutions. Previously known as AmerisourceBergen, our new name, Cencora, unites our 46,000+ team members under one identity in pursuit of a shared purpose: We are united in our responsibility to create healthier futures. : We are united in our responsibility to create healthier futures. AmerisourceBergen is ranked #11 on the Fortune 500 and #24 on the Global Fortune 500 with more than $200 billion in annual revenue.
