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Permanent

Senior Systems Engineer

Bedford
money-bag Negotiable
Posted 1 week ago

Job DescriptionJob Description Senior Systems Engineer, Product Development Engineering

Bedford, MA

Full-time, Onsite

About the Opportunity Our client is seeking a Senior Systems Engineer to join their team in a fully-onsite capacity in Bedford, MA. This is a rapidly growing company dedicated to advancing innovation in healthcare and to tackling the leading cause of death in the Western world - Coronary Artery Disease. This team is tackling a meaningful challenge and is seeking a Senior Systems Engineer to contribute during an exciting stage of growth and transformation.This is a great opportunity for someone who thrives in dynamic environments, enjoys solving complex problems, and wants to make a measurable difference in patient care and outcomes. About the CompanyStage: Series-B FundedTeam Size: Approximately 65 employees and scalingLeadership: Founded and led by strong and experienced leadersTechnology: Novel imaging technologyRecent Milestones: FDA cleared product and a recent $50M investment from a big-name MedTech investorWe’ll share more about the company with qualified candidates after an initial conversation.What You''ll DoLead system integration and VandV efforts for complex electromechanical medical devices, ensuring traceable requirements, cross-functional collaboration, and regulatory-ready documentation.Collaborate with clinical, regulatory, and external development partners to align system requirements, support integration, and drive verification success.Own system-level verification and validation activities, ensuring traceability to user needs and alignment with regulatory standards.Troubleshoot hardware/software interfaces and resolve integration issues using structured problem-solving methods.What We''re Looking For5+ years of experience in Medical Device Engineering, preferably in Systems / Systems IntegrationHands-on skills in electromechanical prototyping, fixture development, and system-level troubleshootingExperience writing and executing formal test protocolsFamiliarity with requirements management software (e.g., JAMA or similar tools)Knowledge of quality systems (QMS) and regulatory expectations for medical devicesBonus: Full product lifecycle experience, from concept through VandV, design transfer, and post-market supportWhy This OpportunityHighly visible role with real impact on patient outcomesJoin a fast-paced, innovative environmentGrowth potential — this is a role with both challenge and trajectoryCollaborate with a mission-aligned, experienced teamCompetitive compensation + benefits

About UsWe’re a specialized recruiting firm serving as a trusted advisor to leaders in medical technology innovation. We prioritize relationships over transactions, and support candidates through every step of the process.All applications are reviewed directly by a human, and we treat every candidate’s goals with care and respect.

Ready to Learn More?Apply through this posting or reach out to us directly.We’ll share additional details with qualified candidates after an initial screening ..... full job details .....

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