R&D Engineer - Pharma/Medical Device (France)

Resourcing Life Science; France; Sur place; EUR 60 000 - 85 000; Plein temps

Résumé du poste

Resourcing Life Science is seeking an experienced R&D Engineer in France to lead design and development of medical device solutions, translating clinical concepts into precise technical requirements and blueprints.

You will collaborate with manufacturing, QA and regulatory teams, supervise experimental components, DOE-driven process optimization, and validation activities across pre-clinical and clinical evaluation programs.

Qualifications

• Min 4 years as R&D Engineer in Pharma or Medical Device plant.
• Engineering degree required.
• Fluent English required.

Responsabilités

• Architects and executes medical device solutions by translating clinical concepts into technical requirements.
• Curates materials, manufacturing workflows and external partners to meet design objectives.
• Directs fabrication of experimental components for engineering assessments and trials.
• Designs scalable production workflows and identifies critical variables using DOE.
• Authors work instructions, SOPs, and manages verification/validation protocols.
• Creates proprietary test methods and simulated-use models with lab staff for validation.
• Performs bench testing and competitive analysis to finalize verification and validation.
• Educates teams on new design architectures and manufacturing processes across departments.
• Manages project capital and conducts cost-benefit analyses.
• Collaborates with Manufacturing, Quality and Regulatory to align with standards and guidelines.

Connaissances

Fluent English

Formation

Engineering degree

Description du poste

Resourcing Life Science is seeking an experienced R&D Engineer in France to lead design and development of medical device solutions, translating clinical concepts into precise technical requirements and blueprints.

You will collaborate with manufacturing, QA and regulatory teams, supervise experimental components, DOE-driven process optimization, and validation activities across pre-clinical and clinical evaluation programs.