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Werfen is seeking a Senior Manager, Reagent & Assay Development to lead a team of scientists in immunohematology R&D from concept to commercialization. The role oversees ABO/Rh typing, antibody screening/identification, DAT/IAT, and rare antigen reagents, ensuring regulatory and quality compliance.
The ideal candidate brings deep immunohematology expertise, strong leadership, and commercialization experience within regulated IVD environments, with a track record of delivering cross-functional
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.
The Senior Manager, Reagent & Assay Development will lead a team of scientists in the scientific and operational development of immunohematology in‑vitro diagnostic (IVD) reagents, assays, and supporting technologies from concept through commercialization. This role is responsible for managing cross-functional development activities related to blood grouping, antibody screening/identification, compatibility testing, and transfusion diagnostics while ensuring compliance with applicable regulatory and quality requirements.
The ideal candidate combines deep technical expertise in immunohematology and assay development with strong leadership, project management, and commercialization experience within regulated IVD environments.