Job Summary:   Directs the project team in a manner to achieve the business results expected. Reporting to the Sr. Director of R&D

If you’re a QC expert when it comes to manufacturing, Immucor has an exciting opportunity for you! We are looking to hire a Quality Control Technologist III  medical device, and/or the pharmaceutical industry. This critical role will Lead QC stability projects, perform Incoming, In-process, final release and stability testing in the Quality Control Laboratory. Act as Team Lead in the QC lab to assist supervisor and Director in daily operations of the Quality Control Laboratory and provide guidance to the QC staff.   This position is

Position Summary: The Cuvettes Team Leader supports daily production and inventory management ensuring quality, production, efficiency, and timely delivery of existing and new/modified products to stock.  As directed, the Cuvettes Team Leader also leads department staff in assigned daily tasks in support of manufacturing activities.   The pay range for this role is $28-$31/hr, depending on experience.

Position Summary: The Procurement Manager is responsible for the tactical and strategic execution of procurement activities at the site level. This role oversees a team of buyers and ensures the timely sourcing of raw materials, components, and finished goods required to support production and business continuity. The Procurement Manager serves as the primary liaison with key suppliers, ensuring alignment on quality, delivery, pricing, and performance expectations, while driving continuous improvement and risk mitigation within the supply base.

Position Summary: Under the direction of the department Director oversees the day to day management of the marketing staff for the product line.  Prepares strategic marketing activities and programs for all supported products.  Provides marketing assistance and support to affiliates, distributors and customers.

Position Summary:   Responsible for ensuring total customer satisfaction within the Werfen installed base.  Perform installations, validations/verification and training on Werfen analyzers.  Provide on-going clinical support, customer education and consult with customers regarding matters of regulatory requirements and compliance.    Amazing Total Rewards for our Clinical Applicants...

Role Summary: The Regulatory Affairs Manager II leads the company’s post‑market regulatory program to ensure global compliance for commercialized IL-labeled medical devices and manages a team of regulatory professionals in this endeavor. This leadership role owns all elements related to post-market regulatory compliance to meet worldwide regulatory requirements, including vigilance reporting, recall (product correction and removal) management, on-market product change assessment, and the post-market surveillance (PMS) program. The manager also develops people, builds processes, and represents Regulatory Affairs during management reviews,...

Job Summary   The Supervisor of VLPCC (Vialing, Labeling , Packaging and Controlled Components)is responsible for ensuring the consistent execution of departmental procedures, maintaining high standards of product quality, and supporting day-to-day manufacturing activities in compliance with cGMP, GDP, and safety standards. This position requires strong technical knowledge, leadership skills, and a commitment to continuous improvement in all facets of production. - This position serves as the bridge between strategic leadership and hands-on execution, ensuring that every batch...

Position Summary:   Under supervision, responsible for product cost oversight, operations income statement detail, and inventory analysis. Prepares all related reporting information. Performs financial analysis and participates in special projects, as required. 

Position Summary:   Fully competent in one or more scientific/technical areas.  Plans and conducts scientific as­ signments requiring mastery of specialized techniques.

Job Summary   Reporting to the Engineering Shared Services (ESS) Manager, individual must be able to program, assemble, and assist in the building of engineering models and prototypes, including performing rework to manufactured components as needed. Individual shall work in close coordination with the Model Shop Supervisor.  The individual shall be able to operate all Model Shop equipment including equipment set-up and programming required for end-to-end fabrication of a variety of high-precision components, test fixtures, and speciality tools or jigs. Individual shall lead model shop CNC-Machine activities,...

Job Summary   Provides analytics and business intelligence insights to enable the North America Commercial Operations leadership team to make informed strategic decisions that drive revenue. The role will act as a consultant to Senior Leadership of Commercial Operations with a focus on reporting, analytics and fostering strong relationships with business partners (eg. Sales, finance, IT). He/she will be looked upon to gather data and perform ad-hoc analyses for the business, develop insights that drive actions and draw upon experience to identify new areas for growth or improvement.

Position Summary: Performs formulations of Clinical Chemistry, Co-Oximeter, and/or Coagulation controls and reagents using various automated and manual techniques. Formulations are to be performed in accordance with established Quality Standards and GMP requirements

Overview:   To learn the importance of employment law and compliance and to understand the day-to-day operations of an efficient Human Resources Department.

Job Summary   Autoimmunity Sr. Managers are responsible for managing the overall operations, business results and performance for their assigned department(s). Responsible for department functional plans, determining current and future position profiles and staffing needs, proposing and managing department budgets, performance metrics and reporting, analyzing operations to identify gaps, ensure compliance, safety, and ongoing process improvements, as well as leading and developing lower-level management staff and high performing teams.  

We are looking to hire a Biologics Procurement Manager who will manage all tasks and functions associated with Biologics Procurement and Manufacturing Training. This includes managing the supply of red blood cells and other blood products needed for Werfen's Red Cell and Capture product line. This person will also manage activities associated with training new employees and cross-training or re-training current employees as needed for Red Cell Processing, Monoclonal Production, Production Support, Controlled Components, Solid Phase, Vialing and Packaging. If you’ve got the necessary skills and experience to excel in this position, we want to hear from you. Apply...

Job Summary The Assay Development Scientist III Performs a variety of tasks, including supervisory activities, associated with the development of new products and new manufacturing process-es, the investigation into and implementation of product and process changes, and the transfer of new products and processes to the manufacturing departments. Oversees and provides leadership to cross functional development team in developing new products using Design Controls. Works at strategic and tactical levels by participating in identifying resources for the department including facility, equipment, personnel, and budgetary...

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...

Position Summary:   Responsible for ensuring total customer satisfaction within the Werfen installed base.  Preform installations, validations/verification and training on Werfen analyzers.  Provide on-going clinical support, customer education and consult with customers regarding matters of regulatory requirements and compliance. 

Position Summary:   This position is responsible for the successful implementation of advanced Werfen digital solution(s) for new and existing Werfen customers in collaboration with the Applications implementation team. This includes but is not limited to completion of all required post sale technical implementation activities, ensuring the product application/solution functions to specifications. Ensures customer satisfaction during installation, validation, integration and go-live processes.