Senior Systems Engineer - Medical Technologies - Oxford

Newton Colmore Consulting; Oxford; On-site; GBP 50,000 - 70,000; Full time

Job summary

A pioneering medical technology company in Oxford is seeking a Senior Systems Engineer to contribute to the development of advanced implantable therapeutic systems. The role requires a background in medical device development, coordination of system architecture, and collaboration with cross-functional teams. Candidates should be familiar with ISO standards and possess strong problem-solving and communication skills, aiming to make a significant impact in a regulated environment.

Qualifications

• Background in medical device development, particularly within implantable or regulated systems.
• Familiarity with ISO 14971, ISO 13485, and verification methodologies.
• Experience working in collaborative teams to address complex technical challenges.

Responsibilities

• Own system architecture, documentation, and compliance across complex platforms.
• Define design inputs and manage system-level requirements.
• Support verification and clinical activities and ensure seamless integration with software, hardware, and quality teams.
• Lead technical investigations and support regulatory submissions.

Skills

Medical device development

Detail-oriented mindset

Strong communication skills

Proactive problem-solving abilities

Job description

Overview

Senior Systems Engineer - Cutting-Edge Medical Technologies - Oxford. This role is with a pioneering medical technology company based in Oxford, contributing to the development of advanced implantable therapeutic systems and coordinating system architecture, documentation, and compliance across complex platforms from concept through clinical application.

Responsibilities

• Own system architecture, documentation, and compliance across complex platforms.
• Define design inputs and manage system-level requirements.
• Support verification and clinical activities and ensure seamless integration with software, hardware, and quality teams.
• Maintain traceability across design and risk documentation.
• Lead technical investigations and support regulatory submissions.
• Apply systems engineering and risk analysis expertise to drive safe, effective solutions in a fast-paced, regulated environment.
• Collaborate in a multidisciplinary environment focused on implantable therapeutic technologies, with scope to support other programmes as needed.

Qualifications

• Background in medical device development, particularly within implantable or regulated systems.
• Familiarity with ISO 14971, ISO 13485, and verification methodologies.
• Strong communication skills and a detail-oriented mindset.
• Proactive problem-solving abilities and experience working in collaborative teams to address complex technical challenges.

How to Apply

If you're looking to make a meaningful impact in a high-accountability setting—where innovation meets clinical application—this could be the next step in your career.

Alternatively, submit your CV and a member of our team will be in touch.