Verification & Validation (V&V) Engineer R&D
Miejsce pracy : Żywiec
Your responsibilities
- Plan, execute, and document verification and validation activities for medical devices throughout the product lifecycle
- Develop and review test protocols, test plans, and validation reports in compliance with regulatory standards such as MDR, ISO 13485, and IEC 60601
- Perform risk assessments related to verification and validation processes
- Collaborate with R&D, Quality Assurance, Regulatory Affairs, and Manufacturing teams to ensure product compliance and quality
- Utilize tools such as TestStand, LabVIEW, or similar for automated testing and data acquisition
- Manage and maintain test equipment and validation environments
- Analyze test data, identify issues, and implement corrective actions
- Continuously improve verification and validation processes to increase efficiency and effectiveness
Our requirements
Bachelor’s or Master’s degree in Engineering, Medical Technology, or a related fieldProven experience in verification and validation in a regulated environmentKnowledge of regulatory standards such as MDR, ISO 13485, IEC 60601, and risk management principles is a plusHands-on experience with testing tools and software such as TestStand, LabVIEW, or equivalentFamiliarity with statistical analysis tools and data analysis softwareExcellent problem-solving, organizational, and communication skillsAbility to work independently and collaboratively in a multidisciplinary teamWhat we offer
A great job opportunity in an international fast growing business as a leader in Surgical tables, Hospital Beds, Surgical Equipment and Patient Positioning Accessoires within the Reinsberg GroupTalent development, professional certification opportunities, continuous learning as well as internal and external training opportunitiesAn exiting position reporting directly to the R&D ManagementA collaborative and dynamic work environment with a high skilled and passionate teamCompetitive salary packages with flexible working hoursBenefits
sharing the costs of sports activitiesprivate medical caresharing the costs of professional training & courseslife insuranceflexible working timeintegration eventsparking space for employeesextra social benefitsholiday fundschristmas giftsemployee referral programFAMED Żywiec sp. z o.o.
FAMED Zywiec is a member of Reinsberg Group, an international MedTech Group and forward thinking healthcare provider in the field of medical devices dedicated to developing and manufacturing high-quality solutions. Our mission is to ignite innovation, fuel collaboration, and championing sustainable growth while delivering exceptional value to our stakeholders across the group companies.
FAMED is seeking for a passionate individual who plans, executes, documents verification and validation activities throughout project programs and the product lifecycle, ensuring project timelines, within budget and to meet the companies goals from a high quality and safety standards. Within this role the individual will be responsible to manage project programs across the Group in a multi-disciplinary high enganged R&D team.
Wyrażam zgodę na przetwarzanie moich danych osobowych przez Famed Żywiec Sp. z o.o. z siedzibą w Żywcu przy ulicy Fabrycznej 1, 34-300 Żywiec zgodnie z rozporządzeniem Parlamentu Europejskiego i Rady (UE) nr 2016 / 679 z dnia 27 kwietnia 2016 r. w sprawie ochrony osób fizycznych w związku z przetwarzaniem danych osobowych i w sprawie swobodnego przepływu takich danych oraz uchylenia dyrektywy 95 / 46 / WE (Dziennik Urzędowy Unii Europejskiej nr L 119 / 1 z 4.5.2016; dalej : RODO) dla celów niezbędnych do realizacji procesu rekrutacji na stanowisko wskazane w ogłoszeniu”.
Kandydatów, którzy zgadzają się na przechowywanie swoich aplikacji przez Famed Żywiec Sp. z o.o. w celu przyszłych procesów rekrutacyjnych przez okres 1 roku, prosimy o dopisanie klauzuli : „Wyrażam zgodę na przetwarzanie moich danych osobowych przez Famed Żywiec Sp. z o.o. z siedzibą w Żywcu przy ulicy Fabrycznej 1, 34-300 Żywiec zawartych w moim zgłoszeniu rekrutacyjnym dla celów przyszłych rekrutacji przez okres 1 roku„ Aplikacje bez wymienionej klauzuli nie będą rozpatrywane.