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Scanlan International, Inc., is a medical device company specializing in the highest-quality surgical instruments. Now in our fourth generation, the Scanlan family continues its dedication to providing the best…
Design Quality Engineer ensures medical devices meet regulatory standards by authoring quality documents, writing test cases, and validating requirements for fusion energy and medical technology systems.
Senior Process Engineer at Panther Life Sciences in Pittsburgh designs and scales automated manufacturing for dissolvable microarray patches used in drug delivery and skin health, ensuring cGMP compliance and commercial viability.
Manages quality assurance and regulatory affairs for a digital therapeutics company, ensuring compliance with medical device standards (ISO 13485, GMP) and handling domestic/international approvals for software-based medical devices.
Position Summary: This position is responsible for directing the work activities and overseeing all manufacturing through shipping processes within the organization. Establishing and ensuring the Safety, Quality,…
Leads quality engineering initiatives for medical device products in Stryker's Endoscopy division, ensuring regulatory compliance and continuous improvement through CAPA, risk management, and audits.
Senior Manager - Customer & Technical Operations - ANZ & East Asia About Stryker At Stryker, we are driven to make healthcare better. As a global leader in medical technologies, we partner closely with…
Ensures supplier quality for medical devices by auditing processes, resolving defects, and enforcing compliance with ISO 13485 and CFR 820 using Six Sigma and PPAP tools.
Senior Engineer in Design Assurance for orthopedic medical devices, leading risk management, usability engineering, and design control documentation in a regulated environment.
Oversee global regulatory compliance for medical device logistics, ensuring adherence to environmental, packaging, and battery regulations across distribution networks.
Oversee quality assurance for medical devices and combination products, ensuring compliance with regulations during design transfer, manufacturing, and lifecycle changes.
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our…
At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down…
Salary Range: $90,800.00 - $151,300.00 Job Description: Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking projects from rapid prototype into high volume production. Our…
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve…
We anticipate the application window for this opening will close on - 31 Jul 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
We anticipate the application window for this opening will close on - 30 Jul 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
Job Description: Summary Innovation and product development are central to Orascoptic's growth. Our product development team designs and develops products used by dental and medical professionals every day,…
Manages EU and global regulatory submissions and compliance for medical devices under MDR 2017/745, coordinating with notified bodies and health authorities.
Oversee quality assurance and compliance for a plastics injection molding manufacturer, ensuring adherence to ISO 13485 and FDA 21 CFR Part 820 in a regulated medical device environment.
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