Permanent: Technical Project Manager
Location: Cambridge
Hybrid
Competitive Salary: £55,000 - £65,000

As a Technical Project Manager lead the development of cutting-edge healthcare technologies that transform lives. You’ll combine innovation and regulatory expertise to bring breakthrough medical devices to market.
From concept to launch, you’ll oversee the full product lifecycle, ensuring our devices meet the highest safety and compliance standards. If you thrive on managing complex projects and delivering meaningful results this is a great position. Experience working with ISO standards and mechanical, electronic, and medical devices is essential.
Your passion for engineering, product development, and innovative problem-solving will drive you to excel in this innovative environment. A proactive mindset, strong attention to detail, and dedication to producing top-quality outcomes are essential.
 
Main duties / key responsibilities:
 

• Leading project teams in the medical device and life sciences sectors to achieve client and company goals, ensuring all project objectives are met effectively.
• Overseeing project budgets, scope, and quality to ensure projects are delivered within agreed parameters and meet established standards.
• Developing project plans, estimating costs, and drafting proposals with input from colleagues, subject matter experts, and the sales team.
• Serving as the primary client liaison to foster trust and build enduring relationships through a professional and reliable approach.
• Mentoring and supporting team members, particularly junior staff, to help them grow their skills and gain experience in project management.
• Engaging in business development activities by networking, representing the company, and contributing to or leading new proposals.

 
Essential:

• A technical degree in mechanical engineering, biomedical engineering, product design, physics, or a related field, or equivalent professional experience.
• Demonstrated success in leading the design and development of medical devices, managing projects from initial concept through to production in a manufacturing or consultancy setting.
• Extensive experience with healthcare and medical products, working under ISO 13485 standards or equivalent FDA regulatory requirements.
• Knowledge and application of industry standards and regulations, such as ISO 13485, 21 CFR Part 820, ISO 14971, IEC 62304, and IEC 62366.
• Experience in managing device transfer to manufacturing, including industrialization using high-speed automated assembly processes.

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