Hardware Program Manager

Porto
Technology – Research & Systems /
Full Time /
Hybrid
You will join our dynamic and highly skilled Systems team where you’ll play a pivotal role in the development of medical devices. You'll be at the intersection of hardware engineering, manufacturing, software, quality, and regulatory affairs teams, playing an instrumental role in bringing groundbreaking products from concept to reality, all while enjoying a vibrant and collaborative work environment.

We’re looking for someone with experience developing new devices with the proper mindset of combining a theoretical approach with hands-on prototyping and testing. You’re experienced working on all product stages from research and development to design and manufacture.

You will naturally strive for innovation, have sharp analytical skills and have a pragmatic and fast-paced work structure. Creativity, adaptability, and technical knowledge in certain aspects of device development are crucial to this role.

What you´ll do:

    • Resources and timeline alignment with key stakeholders and leadership.
    • Apply Agile methodologies towards medical device hardware and software development.
    • Work with product teams to define milestones and prioritize short-term goals along a product development path.
    • Document project plans, scope, and decisions, as required by medical device industry standards.
    • Facilitate technical discussions at disciple intersections (i.e. Hardware/Software, Hardware/Manufacturing, etc) that require close collaboration.
    • Support members, clients, and engineering teams with special projects

What you need to have:

    • A bachelor's degree (or equivalent) in hardware or software engineering
    • 5+ years in a program management role, leading hardware and software teams
    • Have successfully led multi-quarter or multi-year projects
    • Successfully launched or managed large-scale (10ks / 100ks) electronics or electromechanical devices into the US or European markets

Bonus points:

    • Proficiency in the regulatory requirements for medical device development
    • Experience with international suppliers and contract manufacturers
*Please note that this position does not offer relocation assistance. Candidates must possess a valid EU visa and be based in Portugal.