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Test and Verification Architect Drachten Yacht

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Gevraagd

  • Fulltime
  • Ervaren/Expert
  • Nederlands, Engels (talen)

Aanbod

  • Loondienst (vast)
 

Vacature in het kort

Drachten
As a Test and Verification Architect, you will ensure the right hardware verification strategy for medical and non-medical devices. Leading verification work packages, you will assign ownership within the team and help solve design issues. You will also provide technical expertise in design reviews and risk management. Optimizing the verification process is key, as is mentoring the team and building a global network. Communication and effective collaboration within cross-functional teams are vital. Explore further to see the impact you could make.
 

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Functieomschrijving
Test and Verification Architect

You are responsible for
• Ensuring right hardware verification strategy (approx. 70% medical devices; 30% non-medical) by delivering proper test coverage, avoiding gap and overlap for release level requirements
• Identifying and resolving issues encountered during design verification, including support in management of design defects, root cause analysis and corrective actions
• Leading verification work packages and assigning ownership within T&V team
• Ownership of planning, ensuring timely execution of verification activities
• Ensuring high quality verification evidence (including compliance with processes, regulations and standards)
• Providing technical expertise during design reviews and contributing to risk management activities
• Boosting the effectiveness of the team by optimization of verification process
• Building effective global T&V network
• Mentoring and supporting team members within design verification process, development of tests methods and managing test equipment
• Managing stakeholders within and beyond own team, e.g. project managers, quality, development leads
• Effective collaboration and communication within cross- functional teams
Functie-eisen
To succeed in this role, you should have the following skills and experience
• Technical background, preferably electrical engineering, mechatronics, physics or comparable subject
• 3+ years of experience in design verification (medical devices)
• 5+ years of experience in R&D area or research laboratory
• 5+ years professional experience in medical device industry
• Strong understanding of engineering principles, hardware testing methodologies and medical device design and development process
• Deep knowledge of regulations, standards and quality systems, such as FDA regulations, ISO 13485, IEC standards, ISO 17025
• Solid understanding of Design Control • Solid understanding of test method development, MSA methodology/ test method validation, statistical techniques
• Strong leadership skills and project management skills
• Excellent written and verbal communication skills for documenting test plans, reports, and collaborating with cross- functional teams
• Strong analytical skills (careful data analysis, effective research, creative thinking and efficient problem solving)
• Excellent project management skills, including the ability to manage multiple priorities
• Strong sense of ownership, passionate, fast learner
• Good practice of Windchill and Minitab is an advantage
• Ability to work in team flexibility in order to work with and provide support for number of people,

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