Medical Product Development Lead (ISO 13485) – On-Site

Platform Recruitment; Warwick; On-site; GBP 65,000 - 95,000; Full time

Benefits offered by this job

Competitive salary and bonuses

37-hour week with early finish on frID

Contributory pension

Private health insurance (seniority)

Cycle-to-work

Team events

Job summary

Platform Recruitment is seeking a Medical Sector Manager for on-site work at the West Midlands development studio. You will lead cross-functional teams delivering medical product development projects under ISO 13485, with focus on cost, schedule, and quality targets.

The role requires a Mechanical Engineering degree (1st or 2:1) and strong commercial acumen, plus hands-on experience with CAE tools and high-volume manufacturing processes. On-site presence is essential.

Qualifications

• Proven experience delivering medical product development projects under ISO 13485 or equivalent.
• Strong commercial awareness and budgeting/quoting of complex projects.
• Excellent communication and client relationship-building abilities.

Responsibilities

• Lead and manage medical and scientific product development projects within an ISO 13485 framework.
• Oversee budgeting, scheduling, and risk control across projects.
• Act as technical lead across mechanical, electronics, software, and design teams.
• Support business development through proposals, client presentations, and partnerships.
• Represent the organisation at industry conferences, trade shows, and seminars (including international events).
• Contribute to marketing and thought leadership with presentations and case studies.
• Foster a culture of innovation, quality, and engineering excellence.

Skills

Medical product development

Commercial awareness

Client relationship building

Leadership

Communication

Education

Mechanical Engineering degree (1st or 2:1)

Tools

CAx/CAE tools

Design validation

Job description

Platform Recruitment is seeking a Medical Sector Manager for on-site work at the West Midlands development studio. You will lead cross-functional teams delivering medical product development projects under ISO 13485, with focus on cost, schedule, and quality targets.

The role requires a Mechanical Engineering degree (1st or 2:1) and strong commercial acumen, plus hands-on experience with CAE tools and high-volume manufacturing processes. On-site presence is essential.