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Lead the design and development team for implantable infusion pumps, ensuring full compliance with global medical device regulations. Manage the product lifecycle from design input and verification to manufacturing transfer and regulatory submissions.
Responsibilities
- Lead the design and development team for implantable infusion pumps, ensuring full compliance with global medical device regulations. Manage the product lifecycle from design input and verification to manufacturing transfer and regulatory submissions.
Requirements
- Requires a Master's degree in Engineering or Technical Sciences with at least 8 years of medical device experience, including 3 years in leadership. Deep expertise in FDA, EU MDR, and ISO standards for active implantable devices is essential.
Key Skills
About Biotalent
BioTalent connects the global life sciences and technology community with the talent, leadership and workforce intelligence to push the boundaries of innovation in STEM and accelerate performance at every stage of growth. Through BioTalent, we deliver flexible, scalable hiring solutions built around your people strategy. Through BioX, we secure the executive talent that defines a company's trajectory. And through Talent Science™, we provide organisations with the quantitative workforce intelligence to know exactly who they need — before they start hiring. Our expert consultants focus on specialist areas including Research & Development, Data Science & AI, Clinical, Regulatory, Medical & Drug Safety, Medical Communications, Engineering & CQV, Manufacturing & Operations, Quality and Commercial. BioTalent is global, with offices in the UK (London), Europe (Munich, Zug, Basel) and across the USA (New York, San Diego, Miami and Boston). We are part of The IN Group, a collection of six
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