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Werfen

Global specialized diagnostics provider

Team Manager - Integration Engineering

Engineering LeadershipConfirmed live in the last 24 hours
Full-timeNorcross, GA, USANo salary listedIn-person

About the Job

Requirements

  • A Master's degree (MA), or an equivalent combination of education and experience, is required.
  • A science or engineering degree is required; Biomedical Engineering is preferred.
  • At least 10 years of related work experience is required, though management may substitute relevant work experience for a degree and/or make exceptions to the experience requirement.
  • Advanced knowledge of the design control process for medical devices is required; in vitro diagnostics experience is preferred.
  • Strong verbal and written communication skills related to complex biological concepts and technical documentation are required.
  • Intermediate proficiency in Microsoft Office, including Word and Excel, and specialized systems including TrackWise, MasterControl, and SharePoint is required.
  • The ability to maintain records and work revisions according to procedures and processes by following current Good Documentation Practices is required.

Responsibilities

  • Lead Integration Engineers through technical planning and execution of system integration engineering and verification activities across assay, reagent, software, hardware, and instrumentation interfaces.
  • Expand team depth through mentoring, shared methods, knowledge transfer, and performance management.
  • Build Integration Engineer team capability in systems thinking, design controls, verification strategy, scientific and statistical methods, technical writing, traceability, risk management, and investigation practices.
  • Provide people leadership of Integration Engineers to support technical execution, including assigning work based on competency, removing technical barriers, providing timely feedback, and planning development.
  • Apply requirements-based, risk-based, and evidence-driven approaches to verification planning, execution, analysis, and reporting.
  • Assess integration and verification readiness by evaluating requirements testability, equipment and method readiness, dependencies, technical risks, and availability of qualified resources.
  • Review and approve verification and validation deliverables by evaluating assumptions, methods, acceptance criteria, analyses, traceability, and conclusions for scientific and engineering rigor.
  • Integrate design control, documentation, traceability, and procedural requirements into technical execution.
  • Collaborate with Regulatory Affairs to ensure compliance with relevant industry standards and regulations.
  • Use data, experimentation, structured investigation, and cross-functional expertise to resolve complex system and product behavior.
  • Identify technical issues and ensure timely evaluation, escalation, and resolution based on product risk and project impact.
  • Facilitate advanced troubleshooting and root-cause analysis using system data, experimental evidence, structured problem solving, and cross-functional expertise.
  • Coordinate project deliverables with Systems Integration Management, the Project Management Office, and other cross-functional teams to meet milestones.
  • Perform other duties and responsibilities as assigned.

Desired Qualifications

  • Experience with in vitro diagnostics is preferred.
  • A degree in Biomedical Engineering is preferred.

About the Company

Werfen

Global specialized diagnostics provider

Werfen focuses on in vitro diagnostics, offering specialized diagnostic solutions for healthcare. It provides tests and instruments for areas like hemostasis (blood clotting), acute care diagnostics, and autoimmunity, used by clinical laboratories to detect and monitor diseases. The company's products combine diagnostic assays, reagents, and instrumentation that run in laboratory workflows to produce actionable patient results. Werfen differentiates itself through its long-standing family-owned heritage, strategic growth including the 1991 acquisition of Instrumentation Laboratory, and a global footprint that spans 30 countries with active presence in more than 100 territories. The goal is to improve patient care by expanding access to accurate, high-quality diagnostic tools and services while maintaining a strong commitment to quality and specialized solutions.

Company size
1,001-5,000
Company stage
Debt Financing
Total funding
$550M
Headquarters
Barcelona, Spain
Founded
1966

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