NSF is seeking a certified Independent Contractor Medical Device ISO 13485 Lead Auditor with expertise in medical device sterilization processes to join our growing team. This remote opportunity offers flexibility, independence, and the chance to work with leading
Work Flexibility: Hybrid What You Will Do / Roles & Responsibilities As a member of the Global Product Engineering team you will gain in depth knowledge about Stryker’s Trauma & Extremities portfolio. You will learn how
Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day,
Job Description: Global Commodity Manager Location: Chotěboř, Czech Republic ESAB is a global leader in welding and cutting technologies. Within our GCE Division, Global Sourcing plays a key role in building a competitive, resilient, and high-performing
Acute Care Technology At ZOLL, were passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in peoples lives. Our medical devices, software and related services are used
Regulatory Affairs Specialist Business Unit: Draeger Medical Systems, Inc., Job-ID: 1284 Location: Andover Function: Quality Work Location: Hybrid Employment Type: Permanent The Job Responsibilities The Regulatory Affairs Specialist will work hybrid in our Andover, MA office.
The Sr Business Development Manager, Antibody Discovery Services will work to establish Twist’s market position for the Biopharma discovery services group. Developing strategic goals, building key customer relationships, identifying new business opportunities and partnerships, negotiating and
As a result of the combination of the BD Biosciences and Diagnostic Solutions business with Waters Corporation (NYSE: WAT), by applying to this role, you will be applying for a position with Waters. Waters is a
Core Hours: Monday - Friday, 8am-5pm Purpose and Scope The Supervisor Quality Compliance is responsible for management and oversight of the Quality Compliance team within the Quality Assurance Unit to ensure the companys adherence to industry
Location:McMinnville, Oregon Job ID: R0143109 Date Posted:2026-08-27 Company Name:HITACHI AMERICA, LTD. Profession (Job Category):Other Job Schedule: Full time Remote:Yes Job Description: Manager, Manufacturing Engineering - APT Company: Applied Physics Technology Location: McMinnville, OR Status: Regular Full
ABOUT ORGANOX: OrganOx is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University
Who is Prince? Founded in 1959 by Ed Miller near Chicago, Prince Industries has grown from a one-man shop into a global manufacturing partner. With seven facilities across the U.S. and China, we serve industries from
Work Flexibility: Hybrid Working hours: 14:00 - 22:00 (Central Europe Time) Deliver, manage, and coordinate execution of routine training activities, supports learning content development, and ensures the effective execution of training processes. This role partners with
Position Overview An Imaging Service Engineer I is responsible for performing scheduled service work on systems within a service area, and some unscheduled work in the service area with the assistance of technical support, as directed
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product
Responsibilities Provides customer support on regulatory issues; Lead CE marking activities (per MDD and EU MDR), including preparation and maintenance of product technical files and clinical evaluations; Develops 510K submissions and obtains FDA approval; Supports product
About This Role Biogen is seeking a qualified candidate for the role of Senior Engineer II in the Device Development group. The Senior Engineer II, Device Development will contribute to the design, development, and lifecycle management
SI-BONE is a fast-growing, publicly traded medical device company that is an industry pioneer in minimally invasive sacropelvic solutions. Our mission is to help patients rise up and reach for the stars, and our vision is
Job Description The Chemistry Manufacturing Controls Manager – Device will support the execution of global regulatory CMC strategies for marketed and development drug-device combination products. This role contributes to the preparation and submission of regulatory CMC
Acorn is looking for an experienced Sr. Mechanical Engineer that can also manage projects to take a technical leadership position and help guide our team of engineers to create innovative, world class products. This position requires