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Job Summary:
A Solution Leader supports the delivery of a given solution within the Digital Factory; defines and coordinates all necessary activities for the commercial implementation of in development products of the Digital Solutions unit with the strategic business units (SBUs), commercial affiliates (technical services and marketing). She/He has a deep understanding of the the industry and target markets,...
We are seeking a results-driven Buyer/Planner/Procurement Specialist to play a key role performing daily activities related to purchasing raw materials, supplies, and finished items. Responsibilities include generation and maintenance of purchase orders, production orders, and placing and expediting orders. In addition, you will monitor and maintain inventory levels of materials and supplies, both purchased and produced. If you are eager to join 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!
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.
Amazing Total Rewards for our Field Service 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
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Amazing Total Rewards for our Field Service 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
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We are looking for a Material Handler to join our shipping/warehouse manufacturing team. This position is responsible for the tasks and functions involving shipping, receiving, storing and distributing materials, parts, supplies, and equipment in our Norcross warehouse facility.
If you have the necessary qualifications for this position, we want to hear from you. Apply today!
Job Summary
Autoimmunity Sr. Managers are responsible for the overall performance and business results of 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, ensuring compliance, safety, and ongoing process improvements, as well as leading and developing lower-level management staff, other direct reports, and high performing teams. Ensures business goals, deadlines and performance standards are met. Collaborates...
Position Summary:
Responsible for technical user support and security in the company's local area networks. Maintains hardware and software on the company's network servers and user workstations. Monitors and controls data communications equipment and software
Job Summary
The Director of Applications provides strategic leadership and oversight for the delivery and execution of clinical application services across the assigned business unit. This role is accountable for ensuring a seamless customer experience throughout the deployment, implementation, and long-term support of in vitro diagnostic (IVD) instruments and assays within clinical environments. The manager leads initiatives focused on customer satisfaction, retention, and operational excellence, including instrument installation, clinical acceptance, go-live support, and ongoing technical and clinical assistance....
Job Summary:
Develops, recommends and implements document control systems and processes to ensure effective compliance to Immucor’s policies and external regulations. Establishes and implements procedures and policies needed to meet the demands of document control in a regulated medical device company. Responsible for/ supports the Document Control project management for global policies, change control and/or documentation initiatives. Ensure allocation of resources consistent with long and short term objectives. Train department management and staff in compliance with...
Position Summary:
Under general supervision, performs a variety of senior level technical and administrative duties in the production of complex assemblies and instruments involving electrical, mechanical and chemical processes. Participates in preparation and tracking of production and quality objectives, participates in data collection.
The Laboratory Services Superisor performs a variety of tasks and functions associated with the appropriate day-to-day operations of the Quality Laboratories and supervises the performance of a variety of tasks within the division.
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 is 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...
Product Line Support Associate (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, will help develop, manage, and standardize Field Service procedures and reporting processes worldwide. Help evaluate the Service data reported worldwide and serve as a main contact point for Service-related issues. Provide technical service support, training, process, and procedures for Hemostasis Automation Instruments to company affiliates, distributors, and customers. Develop customer satisfaction...
Position Summary:
Performs basic filling and packaging functions, and formulations as required, in support of Coagulation, Clinical Chemistry and Critical Care product lines; uses automated and manual methods in accordance with established Quality standards and cGMP's
Position Summary:
The QC Technologist I is responsible for the execution of a broad range of bench test procedures used in the testing of finished goods prior to release, assisting with investigations of product performance, routine validation studies, and housekeeping within the Quality Control (QC) laboratory. The QC Technologist I maintains the documentation of approved QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards.
Job Summary
Under direction of North America Marketing, this role will plan, schedule and execute digital campaigns and programs. This position requires enthusiastic leadership, coordination, and collaboration skills. This individual is required to lead multi-functional marketing and sales staff to develop high value digital marketing programs. The individual will develop the annual design and calendar of digital marketing initiatives, including campaign development,...
Position Summary:
Under direction of the department manager, provides technical assistance to customers and Werfen field personnel within a product line responsibility. Troubleshoots, over the phone, answers a broad range of technical questions regarding instrument performance, instrument capabilities, QC concerns and other product concerns as required. Assists in the training and direction of new personnel within the department.
Market Access Manager (INOVA Diagnostics, Inc. d/b/a Werfen Autoimmunity, San Diego, CA): On behalf of a worldwide developer, manufacturer, and distributor of specialized diagnostic instruments and reagents for Autoimmunity products and services, responsible for developing and implementing market access strategy and tactics into a continuously evolving healthcare environment. Serve as key contributor of the overall commercialization effort of new and existing Autoimmunity systems and reagents and provide guidance and support on related product development activities and collaboration with key opinion leaders.
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.