Job Summary The Systems Integration Senior Manager at Autoimmunity (AID) is responsible for planning and managing the systems integration team to succcessfully meet company goals and customer needs. In conjunction with the Autoimmunity Leadership team, this position is responsible for developing strategies to meet company goals and ensure the highest quality Autoimmunity products. Fosters collaboration across teams to facilitate technical integration; oversees cohesive development and delivery of systems products. Responsible for building and leading a high performing team, and ensuring compliance with all Quality System and other regulatory, company and administrative...

Summary:   The Electrical Engineering On-Market group has an opening for a Co-Op who will contribute to the development of current generation medical diagnostic instruments. Product development activities include taking concepts through feasibility into engineering and manufacturing prototypes. The candidate should be comfortable both working independently and in project teams with an interest in hands-on laboratory work.

Job Summary The Manager of Customer Standing Orders is responsible for leading the team that sets up, maintains, and renews 12 month reagent standing orders to ensure uninterrupted supply and outstanding service for our in-vitro diagnostics customers. This role owns the end-to-end process from standing order entry through renewal and shipment readiness, ensuring all orders are in the system before the period of performance starts so customers receive timely shipments- and experience no gaps in service.

Job Summary The Document Control Supervisor is responsible for overseeing the daily activities of the Document Control group. Oversees all activities associated with change orders, SAP training sessions, quality plan tasks, document and record processing, metrics, artwork for labeling, and other tasks that help to achieve department objectives. Works closely with other Quality & Regulatory teams, other departments, and management to ensure activities effective operations. Resolves procedural and process issues as well as recommends ares for improvement. Manages direct reports to comply with company policies and meet department goals. This...

We are seeking a Solid Phase Technician to join our manufacturing team. As a Solid Phase Technician you will perform a variety of tasks associated with the manufacturing operations of solid phase plates for Werfen products. If you’ve got the necessary skills and experience to excel in this position, we want to hear from you. Apply today!   This position is not eligible for...

Position Summary: Responsible for leading the process engineering and production support of a product or product line.  Provides technical leadership and support for continuous improvement team efforts focused on process improvement and optimization.  Provides engineering leadership for the design, documentation and implementation of assembly methods, test methods, equipment operation, including specification and optimization.

Job Summary   As a Senior Principal Regulatory Affairs Specialist, you will perform regulatory affairs and quality system support activities associated with the manufacture and distribution of the Werfen product lines for U.S., Canada, and European Union. 

Position Summary Under the general supervision of the Payroll Manager, responsible for processing and administering payroll and benefits.

Job Summary:   The People Coordinator provides essential administrative support to the Total Rewards team and delivers a seamless onboarding and orientation experience for all new hires. This role serves as the primary point of contact for new employees, ensuring they receive clear communication, timely support, and a well-organized introduction to the organization. The People Coordinator also maintains HRIS data integrity, manages pre-employment compliance requirements, and supports general HR operations throughout the employee lifecycle.  

Provide technical product training for employees, customers and distributors. Maintain training records and course materials within the Learning Management System (LMS). Provide innovative solutions in the creation of training programs and tools according to Werfen and regulatory guidelines.  Follow procedures and maintain training records to ensure compliance with the Werfen Quality System.

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. 

This is a Summer/Fall Co-Op position (July - December 2026)    Summary:   The chosen candidate will be assigned within a multi-discipline team with tasks to assist in the design and development of new automated medical diagnostic instruments. Responsibilities include designing, prototyping and troubleshooting clever solutions towards next generation and on market products....

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.    The Electrical Engineering group has an opening for a Fall co-op who...

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.

Position Summary Responsible to manage pre-market regulatory activities required to maintain compliance to US FDA, Health Canada and EU IVD Regulations (EU) 217/46, as well as other country regulatory agencies.  Represents regulatory on design teams, prepares regulatory plans, authors US FDA 510(k)s, Health Canada license and EU Notified Body submissions and interfaces with these agencies through submission completion.  Acts as reviewer on product labeling, including commercial materials such as brochures and presentations, for regulatory compliance.

Position Summary The Specialist, Quality Labeling is responsible for coordinating the review and approval of product related labeling to support Marketing and Regulatory activities.  The Specialist, Quality Labeling will manage labeling projects and track and report on the progress of the projects.  The Specialist, Quality Labeling will manage translation projects and deadlines.  

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.   

Position Summary The Material Handler I is responsible for the safe and efficient movement, storage, and retrieval of materials and inventory within a warehouse or distribution center. This may consist of specific tasks within the warehouse or distribution center, such as but not limited to picking, packing, shipping, conveyor operator, labeling, and other areas.   This is a non-exempt role compensating $19.00/hr. - $24.00/hr. 

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: Responsible for working closely with R&D, Marketing, Material, Operations and print suppliers to create, revise, and release Product Inserts, Packaging Artwork and Labeling Artwork in accordance with regulatory requirements, standards, and Company procedures.  Prepare labeling change documentation (Change Orders), with supporting documentation.  Coordinate with external partners (e.g. Affiliates and other Company site locations, such as  Spain, Japan, China, etc.) and suppliers/consultants.