Senior Verification Architect (m/f/d)
at Beckman Coulter Diagnostics
München, Bayern, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 31 Oct, 2024 | Not Specified | 31 Jul, 2024 | 8 year(s) or above | Communication Skills,Computer Science,Scripting Languages,System Verification,Test Automation Tools,Biomedical Engineering | No | No |
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Description:
Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.
At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.
Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.
As a Verification Architect (m/f/d) at Beckman Coulter, you will be responsible for the verification and validation processes for our Clinical Laboratory Automation System serving clinical diagnostic laboratories. This position is part of the System Test department in Munich and will be hybrid, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.
If you thrive in a multi-functional, fast paced, role and want to work to build a world-class organization— read on.
THE ESSENTIAL REQUIREMENTS OF THE JOB INCLUDE:
- Bachelor’s or Master’s degree in Electrical Engineering, Computer Science, Mechanical Engineering, Biomedical Engineering, or a related field.
- Minimum of 8 years of experience in system verification within the medical device industry.
- Experience with regulated environment (e.g. Strong understanding of FDA regulations and risk management practices). Attention to detail and result oriented.
- Proficiency in test automation tools and scripting languages.
- Ability to lead activities and projects, facilitate discussions and improve processes.
- Demonstrated ability to work effectively in a fast-paced, multidisciplinary team environment and with remote teams.
- Strong written and verbal communication skills in German and English
- There is a possibility to work part-time (min. 32 hrs weekly)
Responsibilities:
- Develop and implement comprehensive verification strategies for our Clinical Laboratory Automation System
- Collaborate with cross-functional teams including software, hardware, and system engineers to define verification requirements.
- Oversee and participate in the creation and execution of test plans, protocols, and reports.
- Utilize advanced analytical and problem-solving skills to identify, troubleshoot, and resolve system-level issues.
- Ensure compliance with FDA regulations and ISO standards throughout the verification process.
- Mentor and provide guidance to junior verification engineers.
- Stay current with industry trends and advancements in verification methodologies.
REQUIREMENT SUMMARY
Min:8.0Max:13.0 year(s)
Information Technology/IT
Engineering Design / R&D
Information Technology
Graduate
Computer Science, Mechanical Engineering, Electrical, Electrical Engineering, Engineering
Proficient
1
München, Germany