Senior Systems Engineer

Werfen

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.

Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Job Summary

The Senior Systems Engineer plays a critical role in defining, developing, and integrating systems and software-level requirements for Werfen Autoimmunity's in-vitro diagnostic (IVD) instruments in accordance with established Inova Diagnostics procedures (Design Control). The Systems Engineer establishes and performs testing (verification and validation) procedures and executes them for products under development and for design changes to existing products. Additionally, the Systems Engineer helps to trouble shoot issues with existing systems/instruments/software/reagents as part of the life cycle management under design control.

This role also involves eliciting, documenting, and managing system and software requirements from various stakeholders, including Marketing, Research, Operations, Sales, and external customers (Voice of the Customer - VOC). The engineer must clearly and effectively communicate design inputs to project teams and provide ongoing support for implementation and clarification.

The ideal candidate possesses technical leadership, hands-on problem-solving skills, and the ability to manage multiple projects in a regulated biotech or medical device environment. Strong attention to detail, excellent communication skills, and proficiency in system-level troubleshooting and lifecycle management are essential.

Key Accountabilities

• 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.
• Responsible for defining, documenting, and managing system and software requirements for a project, incorporating input from various internal and external stakeholders, including Marketing, R&D, Operations, Regulatory, and Voice of the Customer.
• Develops system flow diagrams, architecture documentation, and interface specifications to support system design and integration.
• Participates in and/or performs system integration testing, verification, and validation activities across a project under minimal supervision.
• Plans, 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 maintaining 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.
• Mentors junior engineers and provides technical guidance to project teams.
• Leads technical reviews and supports project planning activities to drive successful execution.

Networking/Key relationships

• R&D teams: Assay Development and Biomarker discovery
• Manufacturing and Operations Teams
• Quality & Regulatory Teams
• Global Systems Support
• Software and Hardware Teams (within Werfen or external)

Minimum Knowledge & Experience for the position:

Bachelor's degree in Systems Engineering, Bioengineering, Mechanical Engineering, or a related field with 6-10 years of relevant experience in systems engineering, biotech, or medical device development. A master's degree is a plus. The ideal candidate would have prior knowledge of System Development Lifecycle (SLDC) concepts and best practices.

Skills & Capabilities:

• Ability to read and interpret the established Werfen procedures.
• Ability to elicit, create, and manage requirements / Design Inputs from various sources (both inside and outside) Werfen and communicate them to the appropriate project teams.
• Ability to create system flow documents from the ground-up.
• 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.
• Six-sigma certification prefered
• Statistical analysis skill preferred (DOE, regression analysis, capability studies)
• Experience in a regulated environment (FDA, ISO 13485, IEC 60601-1).
• Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).

Travel requirements:Up to 10% travel required.

The salary range for this position is currently $110,000- $150,000 annually. Individual compensation is based on the candidate's qualifications for the position, including experience, skills, knowledge, education, certifications, internal equity, budget, and/or other business and organizational needs.

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 NAtalentacquisition@werfen.com for assistance.

We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.

www.werfen.com