Technical Project Manager
Lead multidisciplinary medical device development across hardware, embedded software, cloud services and analytics — from approved requirements to a product ready for manufacturing. Based at Forskningsparken in Oslo.
About Ably Medical
Help turn complex technology into simpler everyday care. At Ably Medical, we are developing LYNG — a contactless monitoring mat placed under the mattress. We bring together medical device engineering, software and clinical understanding to help care teams take a more preventive approach to healthcare. Now, we are looking for a technical leader who can bring these disciplines together and move development from requirements to a product ready for manufacturing.
The Role
This is a role for someone who enjoys both the technical detail and the bigger picture. You will lead multidisciplinary medical device development across hardware, embedded software, cloud services and analytics — and help shape how R&D at Ably Medical is organised and delivered.
In this senior, hands-on role, you will turn approved product requirements into realistic plans, resolve technical trade-offs and integration challenges, and bring internal engineers and external partners together around delivery. Working closely with the management team, you will give the organisation a clear view of progress, risks and decisions needed.
Your Responsibilities
- Lead project scope, milestones, resources, budget, dependencies and technical risks.
- Drive system architecture, multidisciplinary integration and traceability from requirements to test evidence.
- Manage design control, risk management, design reviews, engineering changes and V&V.
- Deliver engineering evidence for MDR CE marking in close collaboration with QARA.
- Lead design transfer with Operations covering manufacturing documentation, test methods, software releases and readiness acceptance.
- Lead and coordinate developers across geographical sites, aligning the team around shared priorities, a common technical direction and delivery goals. Manage outsourced development partners through clear work packages, controlled interfaces and technical acceptance.
- Coordinate R&D capacity, resolve delivery constraints and report progress and resource needs to the management team.
Why Join Ably Medical?
You will have a direct influence on both the product and the way we develop it. The role combines hands-on technical leadership with the opportunity to shape R&D delivery, work closely with the management team and collaborate across engineering, quality, clinical and manufacturing perspectives.
Required Experience and Skills
- 8+ years of experience in similar roles.
- Documented successful completion of ISO 13485-governed development projects for physical products with integrated software, including V&V and design transfer.
- Hands-on CE marking experience under EU MDR 2017/745, including technical documentation, conformity assessment support and QARA collaboration.
- Strong technical project management covering scope, schedule, budget, resources, risks and outsourced partners.
- Strong system architecture and systems engineering across hardware, embedded software, cloud and analytics, including interface control and integration.
- Practical competence in design control, traceability, medical device risk management, configuration and change control, and cybersecurity.
- Relevant technical degree or equivalent documented professional competence.
Language Requirements
- Required: spoken and written English at A-level, or equivalent documented language skills.
- Desired: spoken and written Norwegian at a similar level is an advantage.
Additional Advantages
- Formal project management qualification.
- Experience in technology strategy, overall R&D leadership and people management.
- A relevant Engineering MSc.
How You Will Work
Product Management defines product needs and priorities; you lead the technical work that makes them deliverable. You will collaborate with QARA on controlled approvals and regulatory evidence, and with Operations on manufacturing readiness. Technical sign-off will follow documented competence and the delegated Ably QMS mandate. Your primary workplace will be our office at Forskningsparken in Oslo, with travel to our other sites expected as part of the role.
Tell Us What You Have Helped Bring to Life
Send your CV and a few brief, non-confidential examples of medical device projects you have helped deliver. We are particularly interested in your role, the technical challenges you worked through and the outcomes — including completed ISO 13485-governed development projects, your hands-on contribution to MDR CE marking, architecture responsibilities and design transfer. Please also describe your English and Norwegian language skills.
Send your application to job@ablymed.com. We look forward to hearing from you.
Who you will be working with
Moving society towards preventive healthcare is a multidisciplinary team effort. We are a driven, ambitious and dedicated team, powered by the opportunity to make a real impact on the healthcare sector.
Erlend Kopperud
Esben Elfving
Lasse Mikkelsen