Associate Systems Engineer
About The Position
Werfen's Autoimmunity business line is looking for an Associate Systems Engineer. This role is an exciting opportunity for an early-career engineer to contribute to the development and enhancement of innovative in-vitro diagnostic (IVD) systems that help improve patient outcomes worldwide. As part of the R&D Systems Integration team, you will collaborate with cross-functional partners across software, hardware, assay development, quality, manufacturing, and regulatory functions to support system integration, design control, verification and validation activities, troubleshooting, and risk mitigation initiatives. This role is ideal for a motivated problem-solver who enjoys working in a fast-paced, regulated environment while leveraging analytical thinking, technical curiosity, and strong collaboration skills to help bring high-quality diagnostic products to life.
Requirements
- Bachelor’s degree in Systems Engineering, Bioengineering, Mechanical Engineering, Electrical Engineering or a related field with 0-3 years of relevant experience in systems engineering, biotech, or medical device development.
- Ability to read and interpret the established Werfen procedures.
- Ability to lead, influence, and motivate people without direct authority. Ability to resolve conflict, manage expectations and negotiating skills.
- Excellent written and verbal communication skills for cross-functional collaboration
- Strong analytical and problem-solving skills, including root cause analysis.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
Nice To Haves
- Master’s degree preferred.
- Statistical analysis skills prefered (DOE, regression analysis, capability studies)
- Experience in a regulated environment (FDA, ISO 13485, IEC 60601-1) a plus.
Responsibilities
- Supports multiple medium- to large-sized projects associated with the development of new diagnostic instruments or improvements to existing in-vitro diagnostic instruments in accordance with established standards and procedures, including design control.
- Communicates project status, risks, and technical challenges to team leads and management.
- Participates in and/or performs system integration testing, verification, and validation activities across a project under minimal supervision.
- Executes, and analyzes verification and validation (V&V) activities, applying statistical tools, reliability analysis, and process optimization.
- Supports troubleshooting activities, failure investigations, and risk assessments, identifying root causes and implementing corrective and preventive actions.
- Utilizes data analytics and modeling techniques to optimize system performance.
- Ensures compliance and risk management standards.
- Responsible for contributing to the Design History File (DHF) for system, instrument, and software development projects and contributing to regulatory submissions.
- Participates in technical reviews and evaluations to ensure robust system design and risk mitigation.
- Works closely with Software, Hardware, Assay Development, Quality, and Manufacturing teams to support system integration and performance optimization.
- Provides input on and reviews user manuals, system specifications, and process improvements.
Benefits
- medical, dental, and vision insurance
- 401k plan retirement benefits with an employer match
- paid vacation and sick leave
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
