Overview
Position Summary:
We are seeking a Senior Process Engineer with strong expertise in test system development, LabVIEW programming, and mechanical engineering within a regulated medical device environment.
Using Engineering procedures standard for research and development, carries out assignments associated with research, design, development, support or manufacturing of specific part, processes, software or components of medical diagnostic systems. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Under the general direction of a functional manager, with moderate latitude for self-direction, operates in one or more areas of responsibility within a specific function.
The annual base salary range for this role is currently $, to $,. This is a bonus-eligible position. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.
This role is eligible for medical, dental, and vision insurance, k plan retirement benefits with an employer match, as well as paid vacation and sick leave.
Responsibilities
Key Accountabilities
Essential Functions:
1. Develop and implement automated test systems for product verification and validation.
2. Design and build custom fixtures, tooling, and test setups to support engineering and production needs.
3. Design, develop, and maintain Teststand, Python and LabVIEW-based applications for data acquisition, control systems, and automated testing.
4. Integrate hardware components (sensors, DAQ systems, instrumentation) with software platforms.
5. Apply mechanical engineering principles to design and improve test equipment, fixtures, and manufacturing processes.
6. Create and review engineering drawings, CAD models, and specifications.
7. Accountable for the completion of assigned deliverables in accordance with approved schedules.
8. Authors documentation and participates in activities in support of design control
9. Independently plans, performs & prioritizes tasks that are moderately complex in nature, in alignment with corporate goals.
10. Analyzes and interprets data, identifying trends and formulating the next steps, if required by the function.
11. Identifies product defects and recognizes outliers in results. Can explain and document product defects and their impact.
12. Effectively communicates complex technical information to a cross-functional team in the form of documentation, presentations or technical summaries.
Secondary Functions:
13. May review and provide input to deliverables from other functions.
14. Lead the development and optimization of manufacturing and validation processes.
Skills & Capabilities:
15. Expertise in Teststand, LabVIEW and Python programming and automated test system development.
16. Experience with data acquisition systems, instrumentation, and hardware integration.
17. Knowledge of validation methodologies and regulated environments.
18. Excellent problem-solving, analytical, and technical documentation skills.
19. Solid foundation in mechanical engineering design and analysis.
20. Technically adept and confident.
21. Leadership: Accountability, Decision Making, Influence, Communication.
Qualifications
Minimum Knowledge & Experience Required for the Position:
Education:
22. Bachelor's degree in Engineering, Science or a related field
Experience:
23. Eight years of product development or relevant experience
24. Four to six years of product development or relevant experience for advanced degrees
25. For internal candidate promotion: Demonstrated proficiency in meeting all competencies of current level and acceptable performance history may be used in lieu of experience
26. In vitro medical device experience highly desired.
Additional Skills/Knowledge:
27. Language: Proficiency in English language required
International Mobility:
28. Required: No
Travel Requirements:
29. Some domestic and international travel may be required.
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact for assistance.
We operate directly in over 30 countries, and in more than territories through distributors. Annual revenue is approximately $2 billion and more than 7, employees around the world comprise our Werfen