Position Summary: The Sr. Facilities Technician will be responsible for the safe, efficient operation, and maintenance of the site's HVAC systems, mechanical systems, with a heavy concentration on HVAC.  Ensures equipment reliability is maintained at an acceptable level, and downtime is kept to a minimum.  Coordinates and oversees third party contractors.

Summary: The purpose of the cooperative experience is to provide a semester long hands-on experience. Werfen hires students with leadership potential and proven academic success. Ideal candidates will combine technical and business knowledge with analytical strength and creative problem-solving abilities.   

Job Summary   This position is responsible for high-speed processing of customer offers and field personnel task requests for the Commercial Operations Organization. The role is also accountable for facilitating requests for proposal responses, pricing proposal approvals, supplies and service contracts review, negotiations, analysis, and reporting for business decision...

Position Summary: Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Microbiology controls and reagents using various automated and manual techniques in accordance with established Quality standards and GMP requirements

Job Summary   At Werfen, marketing is more than messaging it’s the engine that drives innovation, market leadership, and better outcomes for patients worldwide. We are seeking a visionary Director, Worldwide Marketing – Autoimmunity to lead the global strategy for one of the most dynamic areas in diagnostics. This is a rare opportunity to shape the future of autoimmune testing by translating cutting-edge science, emerging market insights, and customer needs into powerful product and marketing strategies that drive global impact.

Job Summary The Director, Strategic Programs & Business Operations supports the COO in coordinating and driving a unified and collaborative approach to strategic programs and critical business processes, across the Hemostasis and Acute Care Business Units and Technology Centers.

Job Summary   Responsible for the overall leadership, management and execution of all IT Solutions activities for North America Commercial Operations. Inclusive of Commercial Marketing, Market Surveillance, Sales Business Partnership, Implementation and Post Sales Technical Support as it relates to IT focused product functionality, solutions, solution architecture and cybersecurity. This role is highly collaborative with customers, internal and field based peer departments.  

Position Summary:   Under general supervision, this position supports the production of medical devices. Duties include a variety of technical support and administrative duties related to complex electro-mechanical test equipment and hand fixtures. Duties are performed within a cGMP/regulated environment with proper documentation of work performed

Overview:   The purpose of the internship is to provide meaningful professional hands-on experience to students with leadership potential and proven academic performance.  Werfen hires students majoring in Engineering and Life Sciences fields into this internship program based on business need.  Ideal candidates will combine technical and business knowledge with analytical strength and creative problem-solving abilities. 

Job Summary Assist Manager, with overseeing the day-to-day operations of Serum Bulk Manufacturing and Monoclonal Production departments with a high degree of attention to detail to achieve quality, compliance, stability and predictability in manufacturing. These processes include, but are not limited to, training and developing of employees, coordinating and scheduling operations, cleaning and sterilization of containers used in production, processing raw material, dilution of solutions/diluents, dilution of final products, intermediate filtrations, and final filtrations. Within in the Monoclonal department, processes include, maintaining Hybridoma...

Senior Software Engineer (Full Stack), Digital Factory (Instrumentation Laboratory Company, a Werfen Company, Bedford, Massachusetts): On behalf of a worldwide developer, manufacturer, and distributor of specialized diagnostic instruments for hemostasis, acute care, and autoimmunity products and services, is involved in all stages and all areas of software development including testing as well as architecture design, code review, and internal tool management. Responsible for the overall development and implementation of front-end and back-end software applications, including back-end design, testing and systems integration.

Position Summary: Responsible for assisting in the planning, coordination, control, and continuous improvement of key components of the Quality Management System (QMS), while ensuring compliance to GMP requirements, FDA & ISO standards, and other regulations as they pertain to the QMS.  The focus of the position is to assist in maintaining and monitoring key Quality Systems.  Duties may include CAPA, Internal Audits, Supplier Audits, Affiliate Audits, External Documents, Management Review, Procedure development, key metric reporting and other key project support...

Job Summary   Performs multiple tasks associated with in-house calibration, repair, and maintenance of Werfen Transfusion instrumentation and parts. Responsible for in-house instrumentation for Neo, Echo, and Manual Capture Workstation systems utilized in customer training, production, product investigation lab and technical training labs.   

Amazing Total Rewards for our Sales Team! - Generous Base Salary + Incentive Compensation - Company Vehicle with Personal Use Allowance - Phone & Internet Reimbursement - 8% 401k Match (dollar for dollar!) - Comprehensive Health Care Benefits - Company...

Job Summary Responsible for overseeing the day-to day activities of the complaint team, works to assure timely case/complaint review and assignment. Responsible for managing the escalation process of potentially reportable complaints with attention to country specific reporting timeliness The QA Manager works with cross func­tional teams to support complaint escalations, investigations and field actions.

Overview:   As part of the harmonization of the Customer Master, this internship position is designed to support the cleanup, restructuring, and implementation of the new structure and tool. To achieve this, the role will require ongoing review of customer accounts and analysis of databases from various master data sets, as well as from other SAP modules. This position will also require the ability to use and interpret reports from both Power BI and Qlik Sense.

Job Summary   The Import Specialist prepares all required import customs documentation with freight forwarders to expedite shipments via truck, air or courier being imported into the country. Reserves space for shipments with freight forwarders based on production needs. Coordinate with Distribution Center, Buyers, and Planning team to efficiently meet production deadlines. Monitor supplier shipments to ensure timely delivery.

Job Summary The Temporary Document Control Specialist III guides, executes, and improves Document Control processes including document changes, quality records control, labeling creation, SAP master data entry, and training record maintenance activities. This role ensures compliance with organizational standards and regulatory requirements and improves the efficiency and quality of Document Control processes. The Document Control Specialist III demonstrates subject matter expertise in document control processes and regulatory requirements. The position is responsible for carrying out activities and facilitating processing associated with change...

Job Summary The International Customer Service Coordinator I is responsible for processing all customer orders in the system with a high level of accuracy.This role involves issuing credit and debit requests, entering system tickets for discrepancies and interacting with the sales team as needed. The primary focus of this role is ensuring precise and timely order entry.

Position Summary:   This position is responsible for ensuring that pre‑market and/or post‑market regulatory activities for digital health products follow applicable domestic and international regulations and guidance. Working independently, with guidance from management or senior regulatory staff, the position will participate in cross‑functional software development meetings; prepare software‑specific submission and registration documentation; assess and document software changes, cybersecurity impacts, and algorithm updates. This role is technically focused and requires advanced skills in...