EU MDR Specialist - Greenwood Village

We are seeking an experienced R&D Engineer with deep expertise in the EU Medical Device Regulation (EU MDR 2017/745) to join our team. · This role will support the design, development, documentation, and compliance strategy for medical devices intended for the EU market. · The id ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partne ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partne ...

Stryker seeking a · Senior Product Environmental Compliance Specialist (Hybrid) · As the Senior Product Environmental Compliance Specialist (Hybrid), you will serve as the division's PEC subject matter expert and process owner, · driving regulatory strategy, compliance execution ...

We are committed to creating an environment where every team member feels inspired, invested, cared for valued and have a strong sense of belonging.Zimmer Biomet is hiring a Sr Regulatory Affairs Specialist in Englewood Colorado to support Paragon 28 product lifecycle management ...

We are seeking a highly organized and quality-driven Sr. Post-Market Surveillance Specialist to lead key quality system processes including complaint handling, CAPA management, field corrective actions, and post-market surveillance (PMS). This role is responsible for ensuring tim ...

We are seeking a highly organized and quality-driven Sr. Post-Market Surveillance Specialist to lead key quality system processes including complaint handling, CAPA management, ...

What You Will Bring · Education and Experience · Bachelor's degree in a relevant discipline (e.g., Engineering, Life Sciences, or related field); or an equivalent combination of education and experience. · 4–6 years of experience in Quality, preferably with a focus on CAPA, compl ...

We are seeking a highly organized and quality-driven Sr. Post-Market Surveillance Specialist to lead key quality system processes including complaint handling, · CAPA management, · field corrective actions, · and post-market surveillance (PMS). This role is responsible for ensuri ...

Thought leadership for organizations in manufacturing industry to become cyber resilient. · Assist clients in understanding today's cyber threat landscape, assess maturity of their cyber security capabilities and define strategy. · Active leadership in aspects of IT strategy rela ...

Act as Sr SME for Short Term Consulting and Solutioning and Process Improvements. Enable execution of potential new engagements. · ...

We are seeking an experienced R&D Engineer with deep expertise in the EU Medical Device Regulation (EU MDR 2017/745) to join our team.This role will support the design, development, documentation, and compliance strategy for medical devices intended for the EU market. · ...

We are seeking an experienced R&D Engineer with deep expertise in the EU Medical Device Regulation (EU MDR 2017/745) to join our team. This role will support the design, development, documentation, and compliance strategy for medical devices intended for the EU market. · The ide ...

We are seeking an experienced R&D Engineer with deep expertise in the EU Medical Device Regulation (EU MDR 2017/745) to join our team. · Lead and support remediation design activities for medical devices in accordance with EU MDR. · ...

EU MDR Specialist - R&D Engineer · Job Description · We are seeking an experienced R&D Engineer with deep expertise in the EU Medical Device Regulation (EU MDR 2017/745) to join our team. This role will support the design, development, documentation, and compliance strategy for m ...

We are seeking a highly organized and quality-driven Sr. Post-Market Surveillance Specialist to lead key quality system processes including complaint handling, · CAPA management, · field corrective actions, · and post-market surveillance (PMS). This role is responsible for ensuri ...

The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for collaborating, planning and executing regulatory activities related to the Bispectral Index (BIS) monitoring product portfolio within the Acute Care and Monitoring operation unit. · This position is located in ...

The Principal Regulatory Affairs Specialist (Pr. RAS) collaborates with cross-functional partners to establish regulatory value and ensure regulatory requirements and strategy are integrated into product development and lifecycle management.A Day in the Life: The role involves pl ...

We anticipate the application window for this opening will close on - 11 Feb 2026.At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access equity for all. You'll lead with purpose breaking down barriers to innovation in ...

We anticipate the application window for this opening will close on - 23 Jan 2026At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. · ...