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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.     We are looking to hire a reliable and safety-minded Shipping Supervisor to play key role coordinating daily activities within our shipping department. This will include scheduling, monitoring, and evaluating department workflow, and implementing process changes as needed to maximize efficiency and productivity. As a Shipping Supervisor, you will be responsible for performing all supervisory tasks and functions associated with the shipping department to ensure a high level of performance in accordance with department procedures. This will involve reviewing and approving training documents, material transfers, and production inventory, as well as coordinating product handling and storage and purchasing supplies. Moreover, you will train new employees and assist the Shipping Manager by developing and implementing department training programs. If you are ready to join an organization where your talents and expertise will be highly rewarded, and if you meet our qualifications to excel in this position, we want to hear from you. Contact us today!   This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Shipping Supervisor – Inventory Control Management  (Logistics / Warehouse)  

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.     The Manager of Quality Operations leads a team of quality specialists and ensures that product is produced that meets design specifications, quality system requirements, and regulatory requirements. This is a hands-on manager role that is directly involved with day-to-day operations required to produce medical device 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 sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Manager, Quality Operations - (Quality Assurance/Document Control/ Quality Operations)   

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.     We are looking to hire a Program Manager. This person will plan and manage small to mid-size product development projects across multiple phases within a large multi-functional product development program; or plan and manage multiple small, related projects which together constitute a program.   They will have regular interaction with all functions and levels of the organization from R&D scientists and engineers, marketing/sales, quality/regulatory, and operations, through executive management.   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 sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Program Manager- R & D/ Medical device / Product development/ Design Control/(R&D)    

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.   We are seeking a driven and results-oriented leader to join our Quality team. In this role, you will be Responsible for the site Quality system and leadership of the site Quality Assurance, Quality Control and Regulatory Affairs organization. - Ensures that a site Quality Management System is established, implemented and maintained for product manufacturing, control, storage, and primary distribution processes in accordance with applicable US Federal Regulations, Regulation EU 2017/746, EN ISO 13485 standards and site Quality requirements. - Act as the QA -RA representative of the site leadership team and, sponsoring  Quality and Compliance-focused culture which embraces Right First Time and Continuous Improvement expectations and directing GMP aspects of plant activities. - Interfaces with other top management personnel to set policy and to assure adherence to these, in addition to governmental standards. - Responsible for the decision on acceptability and release of all site products. - Organizational responsibilities include site Quality Assurance, Quality Control and Regulatory Affairs documentation, and regulatory inspection / customer audit liaison activities. Additional responsibilities include site department budget, hiring and development of personnel, and management of the Quality and RA organization If you are interested in joining an organization where your talents and expertise will be highly appreciated, and if you meet our qualifications to excel in this position, we want to hear from you.   This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.    Sr. Director, Quality Assurance & Regulatory Affairs  

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.   The Quality Engineer is the subject matter expert for Software as a medical device (SAMD) and/or software as an accessory/component to a medical device, and ensures the software is compliant with all regulations.  This role oversees implementation of the project quality management plan(s) and product plans of the organization.  He/She helps to ensure the quality, compliance, and integrity of GXP systems used in the development, manufacturing, and distribution of medical devices / In vitro devices (IVD). The role also manages projects from concept to completion; creates and manages project plan, work cross functionally to ensure completion, and ensure adequate training to impacted areas. He/She works effectively with stakeholders to ensure alignment with business objectives, correct prioritization, and successful project delivery and assists with product and process validations, including protocol and report review.  If you have the required skills, don't wait, apply today!!   (This is NOT AN IT POSITION)   This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Quality Engineer/Medical Device/ IVD Software  

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.    We are seeking a reliable Material Handler to join our Recieving Department. This person will be responsible for performing a variety of tasks involving the shipping, receiving, storing and distributing of materials, parts, supplies and equipment. Understand and comply with any/all guidelines within the Werfen Quality Manual, cGMP, GDP, FDA, ISO, Housekeeping, and Departmental Compliance.   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 sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Material Handler – Receiving (Distribution / Inventory) Warehouse    

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.   We are looking for a Senior Verification Technologist who is responsible for performing complex system tests for development and performance of new and modified consumables, hardware, software, or assays.  The Senior Verification Technologist will be responsible for having knowledge of various test fixtures and strong instrument troubleshooting abilities.     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 sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Senior Verification Technologist – Medical Technologist (Systems Engineering – R&D)   

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.   We are currently seeking a RBC Processing Technologist to join our team. As a RBC Processing Technician, you will perform a variety of activities in the Red Cell Processing Department. Processes red blood cells, formulates red blood cell products into a diluted (bulk) state, and performs in-process testing in an aseptic production environment. Performs production tasks in a cleanroom environment in compliance with Good Manufacturing Practices and Good Documentation Practices.   If you’ve got the necessary skills and experience to excel in this 2nd shift position, we want to hear from you. Apply today!   This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   RBC Processing Technologist - Manufacturing Lab  

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.     We are seeking a Medical Laboratory Technologist II, Technical Specialist to join our Quality Laboratory team. The Medical Laboratory Technologist II, Technical Specialist is responsible for performing a variety of tasks and functions associated with the appropriate day-to-day operations of the Technical Specialist division within the Quality Laboratories. As a Medical Laboratory Technologist II, Technical Specialist, you will ensure strong GMP environment within a very dynamic and changing manufacturing/quality environment. Achieve compliance ready state of each laboratory area. Serve as main point of contact for Laboratory Services. This includes but not limited to the coordination of training, new and incumbent employees on equipment, documentation, product control, product handling, storage, serological duties, chemistries and any other task associated with making sure the products reach the customers. Assist with review and approving of test data, preparing validation documents, writing, reviewing and creating SOPs and OJTs. Overseeing and assisting with special projects.   This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Medical Laboratory Technologist II, Technical Specialist – Quality Laboratory  

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.   This position is responsible for managing the Transfusion and Transplant Technology Center Supplier Management program including supplier qualification and selection, supplier agreements/contracts, supplier relationship management, and supplier reviews. Manages the procurement of all direct materials, supplies, instruments/parts and any indirect materials and miscellaneous items required by Werfen. The Supplier Relationship Manager role is an individual contributor role. Th If you are interested in joining an organization where your talents and expertise will be highly appreciated, and if you meet our qualifications to excel in this position, we want to hear from you. Contact us today!   This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Supplier Relationship Manager(Procurement Department)    

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.   We are seeking a talented and highly motivated Senior Engineer who will participate in software development for medical device applications.  Responsibilities span the software development life-cycle, including requirements definition, design, construction, test, and maintenance.  They will conduct feasibility of proposed designs to determine their ability to function as intended.  Develop and maintain detailed documentation for both internal and external customers.  Operates within defined processes and procedures to identify necessary activities and determine appropriate actions. If you are looking for an opportunity to design, construct, test and maintain complex software products through all phases of software development life-cycle, we want to hear from you. Apply today!     This position is not eligible for sponsorship for work authorization . Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   This position can be based out of Norcross, GA, Bedford, MA, or Warren, NJ Senior Software Engineer (Research & Development- Software)  

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 through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.   TERRITORY: NORTHERN CALIFORNIA; San Francisco, Oakland, Sacramento, Fresno   We are seeking a skilled and hard-working Blood Bank Business Manager (Business Development Sales Representative) to join our team of professionals at Werfen.This person will be focused on taking ownership of assigned customer targets and achieving annual instrument and reagent sales objectives in all targeted Werfen markets within a geographic territory. If you meet our background requirements and are looking to grow your career with an innovative company that rewards hard work and success, this is the ideal opportunity for you!   This position is not eligible for sponsorship for work authorization. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time.   Blood Bank Business Manager - Business Development Sales Representative (Medical)