Clinical Devices SME

About Akkodis

Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis offers broad industry experience, and strong know-how in key technology sectors such as mobility, software & technology services, robotics, testing, simulations, data security, AI & data analytics. The combined IT and engineering expertise brings a unique end-to-end solution offering, with four service lines – Consulting, Solutions, Talents and Academy – to support clients in rethinking their product development and business processes, improve productivity, minimize time to market and shape a smarter and more sustainable tomorrow.

Akkodis is part of the Adecco Group. Our Webstite : www.akkodis.com

Context :

We’re seeking a methodical, detail-oriented Clinical Device SME with strong interpersonal skills to join our Devices, Artwork & Packaging team. You’ll play a critical role in selecting and assessing medical devices used in UCB-sponsored clinical trials across the globe.

Your responsabilities :

• Define and implement strategies for drug delivery devices in clinical trials.
• Act as the subject matter expert (SME) for injection pumps, infusion systems, oral syringes, and more.
• Lead sub-teams dedicated to ensuring proper device selection & evaluation.
• Provide technical assessments for devices sourced by CROs.
• Collaborate cross-functionally with Clinical, QA, RA, Safety, and Device SME teams.

You’ll report to the Head of Device Transversal Services and be part of a global, collaborative team committed to innovation and excellence in clinical research.

Your profile :

• Master’s degree (nursing or medical background is a plus)
• 8+ years' experience in clinical drug delivery device selection
• Deep understanding of medical devices and pharma environments
• Clinical trial set-up expertise (FIH to Phase 4)
• Solid knowledge of EU MDR, 21 CFR Part 820, ISO 13485, GMP/GCP
• Experience in compatibility testing & materials of contact assessment (a plus)
• Strong project management and leadership skills
• Excellent written communication and documentation abilities
• Autonomous, structured, and detail-focused

Why join Akkodis?

By joining the AKKODIS team, you will benefit from:

A personalized onboarding process through a mentoring system Career support from your Business Manager Active involvement in your training plan as well as in your personal and professional development A permanent contract A competitive salary package, including several extra-legal benefits