
Vitrolife · Viby J
At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we h...
At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards
building a family. Together we help our customers and their patients to fulfill the dream of having a baby.
As a Senior Software Engineer at Vitrolife, you will be instrumental in the product development of robust application software for
our advanced IVF-related products. Your responsibilities will span the full lifecycle of software applications, encompassing both
the user interface and core business logic, primarily using C# and WPF.
You will work closely with stakeholders to clarify requirements and translate complex needs into effective, maintainable software
products that are essential in modern assisted reproduction technology.
This role offers you significant ownership: you will drive key product features from concept to release, ensuring adherence to
regulatory standards, and making tangible contributions to solutions that transform patient care in IVF.
IVF-related solutions.
We review applications on an ongoing basis and will close the recruitment once we have found the right candidate. We look forward
to receiving your application.
If you have any questions, please reach out to Recruiting Manager Maria Soler, msoler@vitrolife.com
Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities,
we develop services and products for personalized genetic information and medical device products. We support our customers by
improving their clinical practice for the patient's outcome of fertility treatment.
We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and
services are available in more than 110 countries through our own presence in 30 countries and a network of distributors.
Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products
and services with the vision of fulfilling the dream of having a baby. The Vitrolife AB (publ) share is listed on the Nasdaq
Stockholm.
Hos Vitrolife Group arbejder vi hver dag for at udnytte videnskabens og teknologiens fulde potentiale og dermed nedbryde barriererne for at stifte familie. Sammen hjælper vi vores kunder og deres patienter med at opfylde drømmen om at få et barn. ROLLEN Vi søger en engageret og ambitiøs Senior Hardware Engineer (som kan træde ind i rollen som Technical Product Owner - Hardware), til vores Product Care-afdeling i R&D Medical Devices i Aarhus. I denne rolle vil du have ansvaret for hardware-koordinering og løbende forbedringer af en specifik produktportefølje med fokus på produktforbedringer, produktvedligeholdelse og compliance. Stillingen skal sikre produkternes stabilitet og attraktivitet gennem hele deres livscyklus ved at koordinere og udføre produktændringer, understøtte risikostyringsaktiviteter og samarbejde tæt med andre afdelinger såsom: Udvikling, Produktion, Supply Chain og Regulatory. DIT BIDRAG * Tage det tekniske ansvar for hardware og systemarkitektur på vores Time Lapse-produkter. * Drive change management, løbende forbedringer og root-cause analyser i tæt samarbejde med andre relevante teams. * Vurdere og implementere produktændringer baseret på kundefeedback, kvalitetsdata og nye myndighedskrav. * Gennemgå og opdatere dokumentation for at sikre overholdelse af standarder som IEC 60601, MDR og FDA. * Bidrage til den løbende support af produktion og aftersales-organisationen. * Være aktivt involveret i prioritering af forbedringer og risikovurdering. DINE KOMPETENCER * Uddannelsesmæssig baggrund som ingeniør eller lignende – med stærke analytiske evner. * 5+ års erfaring med hardware – gerne fra medicoindustrien eller andre regulerede industrier. * Bred indsigt og ægte interesse for tværfaglig ingeniørarbejde, herunder elektronik, mekanik, design, proces og produktion. * Erfaring med root-cause analyse, produkt- og designændringer. * Fremragende samarbejdsevner med en struktureret og agil tilgang til arbejdet. * Flydende i både dansk og engelsk, skriftligt og mundtligt. * Motiveres af at arbejde med tekniske udfordringer. * Kendskab til regulatoriske krav og standarder er en fordel (fx MDR, IEC 60601, FDA). HVEM ER DU * Stærk kommunikator, der evner at formidle tekniske forhold klart til både tekniske og ikke-tekniske kolleger. * Analytisk mindset, som gør det muligt effektivt at løse tekniske udfordringer. * Teamplayer der bidrager med samarbejde og støtte i tværfaglige teams. * Løsningsorienteret – identificerer og løser udfordringer proaktivt. * Struktureret og organiseret – sikrer solid dokumentation og opfølgning på vigtige opgaver. * Omstillingsparat og åben for forandring – bevarer en positiv indstilling til løbende forbedringer. * Tager ejerskab og ansvar for leverancer og deadlines. * I stand til at håndtere flere opgaver og prioritere effektivt i et dynamisk miljø. * Motiveres af at hjælpe andre og bidrage til fælles succes. SUCCES I DENNE ROLLE BETYDER * Du sikrer, at eksisterende hardware og Time Lapse-systemer er opdaterede, robuste og fuldt compliance med lovkrav. * Produktændringer og -forbedringer implementeres effektivt og er veldokumenterede. * Du bliver fagekspert (Subject Matter Expert) i vores eksisterende produkter og processer, og understøtter forretningen under audits og compliance-aktiviteter. * Du bidrager til et stærkt samarbejde med medarbejdere bl.a. i afdelingerne; QA, Regulatory, Produktion og Aftersales, så produktet imødekommer både kunde- og forretningsbehov. KONTAKTINFORMATION Vi vurderer ansøgninger løbende og lukker rekrutteringen, når vi har fundet den rette kandidat. Vi glæder os til at modtage din ansøgning. På grund af sommerferien gør vi opmærksom på, at behandlingen af ansøgninger kan tage længere tid og strække sig over august måned. Hvis du har spørgsmål, så kontakt venligst ansættende leder Morten Steffensen på msteffensen@vitrolife.com. Vitrolife Group er en global leverandør af medicinsk udstyr og genetiske services. Baseret på videnskab og avancerede forskningskompetencer udvikler vi services og produkter indenfor personlig genetisk information og medicinsk udstyr. Vi støtter vores kunder med at forbedre klinisk praksis for patientens fertilitetsbehandling. Vi er cirka 1.100 kolleger verden over med hovedkontor i Göteborg, Sverige. Vitrolife Groups produkter og services er tilgængelige i mere end 110 lande – enten via egen tilstedeværelse i 30 lande eller gennem et globalt netværk af distributører. Vitrolife Group er en bæredygtig markedsleder og har som mål at være den foretrukne partner for IVF-klinikker gennem overlegne produkter og services med visionen om at opfylde drømmen om at få et barn. Vitrolife-aktien er børsnoteret på Nasdaq Stockholm.
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