Device Program Lead — Medical Devices, GMP & MDR

Akkodis

Waals-Brabant

On-site

EUR 120,000 - 160,000

Full time

3 days ago

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Benefits offered by this job

Permanent contract

13.92 months of salary

Company car or mobility budget

Flexible cafeteria plan

Hospitalization insurance

Training and development opportunities

Structured onboarding and career talks

Access to technical communities

Referral and business bonuses

Career development across projects

Job summary

Akkodis is looking for an experienced Device Program Lead to drive development, industrialization, and lifecycle management of drug delivery systems in a pharmaceutical environment. You will coordinate cross-functional teams and external partners while ensuring compliance with Medical Device regulations and GMP.

The role requires 8+ years in pharma/medical devices, strong project management, and knowledge of ISO 13485, MDR, and quality systems.

Qualifications

8+ years of experience within pharmaceutical, biologics, and/or medical device industry.

Responsibilities

Lead development, industrialization, lifecycle management of drug delivery systems.
Coordinate cross-functional teams including internal stakeholders and external partners.
Manage technical projects: planning, resources, budgets, suppliers, industrialization activities.
Ensure compliance with Medical Device QMS and regulatory requirements.
Support design verification/validation, process validation, regulatory submissions.