Deployments & references
Technical Delivery, R&D, integrations, commissioning, training
I’ve participated in end-to-end deliveries of automated dispensing cabinets across Finland and international sites. Much of my work has been done in commercial healthcare product development and customer delivery under NDA. For that reason, I describe projects through responsibilities, technical context, and outcomes rather than source code or internal documentation.
Role: Product Owner / Technical Delivery Lead — deployments, integrations, commissioning, training, operational support.
Scale: Dozens of projects including 200+ deliverables in total (multi-site).
Typical scope: Research and development, user requirement translation to the developers and to the customer, commissioning readiness, integrations (patient information systems, pharmacy/consumption control), identity/authentication (AD/domain), training, and operational support.
My GitHub is still growing, but it shows my personal enthusiasm for technology, programming, and experimenting with new ideas. Other work is detailed below in this page.
Public references
Only publicly available sources are linked. Confidential deliveries or research and development work not included.
Kuopio University Hospital (Kaari Hospital)
Early adopter story and user innovation case. (Link)
Approx. 70 cabinets deployed over multiple phases, with several R&D initiatives over a few years.
Estimated total scope/value: €Multi million value (order-of-magnitude estimate; varies by delivery scope and services).
Seinäjoki Central Hospital
Case story includes eMED ICON cabinet count and workflow benefits. (Link)
A small-scale deployment, but strategically important: the customer was open to testing and developing integrations with hospital patient and medication systems. The biggest value for us was hands-on learning — accelerating integration know-how, delivery practices, and real-world feedback for the team.
Hospital Nova (Jyväskylä)
New hospital story: 35 eMED ICON cabinets and integration preparation. (Link)
Delivered devices and supported several R&D / improvement initiatives over a multi-year period.
Estimated total scope/value: tender value range €1.3M–€8.0M. (TED notice)
Note: value range is from the tender documentation; awarded scope and follow-on services may differ.
Odense University Hospital
First-of-its-kind in Denmark (press release). (Link)
A strong learning project in a new customer environment — integrating with new systems and validating delivery practices in real-world use.
Value: accelerated integration know-how, delivery readiness, and practical feedback for the team.
Other deployments (non-public list)
I have contributed to multiple live deployments across Finland and international sites. Due to confidentiality, only publicly referenced projects are linked above.
Finland (selected sites): Kuopio, Seinäjoki, Tampere, Turku, Oulu, Rovaniemi, Jyväskylä (Nova), Mikkeli, Savonlinna, Lappeenranta, …
Denmark: Odense, Esbjerg, Aalborg
Croatia: Zagreb (Merkur Hospital), Zadar, Našice
What I typically owned
Across deployments and R&D work, I owned the end-to-end delivery “glue”: translating needs into work and making sure the result was reliable in production use.
- R&D scope translation: turned user needs and agreements into clear requirements and deliverables for sales and engineering.
- Delivery planning & commissioning readiness (site prerequisites, acceptance)
- Integrations & data flows (patient systems, consumption control, audit trail)
- Identity & access (AD/domain, certificate-based authentication where applicable)
- Training & documentation (internal + customer)
- Operational support & troubleshooting (RCA, production issues, change control)
Product development beyond software
My work has not been limited to product ownership in software development. I have also contributed to physical product development, including mechanical and electrical design coordination, compliance-driven testing, product-level quality assurance, and the finalization of safe and reliable design decisions in R&D.
Physical Product Development & Compliance
I worked at the intersection of software, hardware, mechanics, and regulated product development. Also contributed to the development and finalization of safe, manufacturable, and compliant product solutions in close collaboration with design, production, and supplier teams.
Main responsibilities
- Coordinated cross-functional product development across software, mechanics, electronics, and device subsystems
- Contributed to DFMA-oriented product improvements and practical manufacturability decisions
- Reviewed and approved mechanical parts, assemblies, and technical drawings in product role
- Led and supported design decision-making from R&D through release readiness
- Helped align product development with compliance, safety, and quality requirements
EMC / Immunity Compliance in R&D
I led EMC and immunity compliance work in R&D as part of finalizing safe and standards-compliant product design. Defined test plans, acceptance criteria, and design-change control during hands-on laboratory testing.
Main responsibilities
- Defined EMC / immunity test plans and acceptance criteria for R&D validation
- Executed hands-on EMC and immunity testing in laboratory conditions
- Controlled design updates and technical changes during iterative test cycles
- Evaluated test outcomes and guided design decisions needed for compliance
- Supported the finalization of safe and standards-compliant product design
Product-Level Quality Assurance
I was responsible for product-level quality assurance in an environment where reliability, traceability, and safe release decisions were essential. Quality work linked together requirements, testing, release readiness, risk management, and long-term product improvement.
Main responsibilities
- Defined and reviewed acceptance criteria and release readiness expectations
- Coordinated testing, validation support, and product-level quality decisions
- Linked product development with risk management and traceability requirements
- Investigated issues, analyzed root causes, and supported permanent corrective actions
- Helped ensure that quality, documentation, and operational reliability remained aligned throughout the product lifecycle
PLC-board Compliance and Manufacturer Guidance
I supported PLC-board related compliance and safety work through requirement setting, testing, approval decisions, and practical manufacturer guidance. Worked close to production to ensure that delivered boards met safety and product requirements.
Main responsibilities
- Defined compliance and electrical safety requirements for PLC-board related solutions
- Performed testing and evaluation of boards coming from manufacturing
- Made approval decisions based on test outcomes and product requirements
- Guided manufacturer changes and provided hands-on feedback on-site
- Conducted small-scale process and quality reviews in supplier/manufacturer site
- Supported firmware-related decisions through testing, review, and compliance perspective
