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The Quality Lead for Design and Tech Transfer Strategy oversees the quality and regulatory compliance of IVD assay transfers into manufacturing. This role partners with R&D and operations to ensure robust design transfer processes, regulatory adherence, and continuous improvement of quality systems.
Leads global Design Control and Risk Management quality system processes for medical devices, managing a team of Business Process Owners and driving process improvements across the product lifecycle.


 We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It…
The BP Program Manager leads Warsaw site program coordination, managing multiple strategic projects end-to-end including manufacturing readiness, technology transfers, and process implementation within a regulated medical device environment.
The SDET will design and build a multi-module automated test infrastructure using C# to ensure the quality of medical device software. This role focuses on architecting test frameworks, CI/CD pipelines, and shared libraries within a regulated healthcare environment.
Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries,…
Job Description: SUMMARY: We are seeking a dynamic, strategic, and results-oriented Global Sr. Manager, Procurement to lead and advance procurement operations across a growing global medical device organization. This…
Company Overview Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life…
COMPANY OVERVIEW: Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life…
Own supplier quality and manufacturing quality for consumer hardware, driving root cause analysis, reliability testing, and compliance with ISO standards to prevent defects and improve product performance.
Senior Product Quality Engineer owns supplier quality, manufacturing quality, and product reliability for consumer hardware, driving root cause analysis and improving performance through audits, testing, and data-driven decisions.
Why should you join our success story? Based on patented technology developed at MIT, Harvard Medical School and by the Company, Myomo develops and markets the MyoPro® product line of lightweight, non-invasive, powered…
SALARY: $80,000 - $100,000 SUMMARY The candidate will establish and maintain the quality assurance program to ensure that the products and the quality system are in compliance with cGMP practices, ISO 13485…
Job Title: National Quality Manager Job Location: Atlanta, Georgia We have an exciting opportunity for a National Quality Manager for our AFR Team. The National Quality Manager to lead and oversee the Life Sciences and…
Purpose In-office role; currently 3 days a week in-office. Based in Raleigh, NC. The Education & Training Specialist II, Internal Training, Global Support, will design, deliver, and continuously improve employee…
Develops cloud-based full-stack applications for orthopaedic surgical planning software, focusing on scalable architecture and testing frameworks in a regulated healthcare environment.
Build and ship full-stack features in a regulated healthtech AI product that turns clinician consultations into verified documentation using speech-to-text and LLMs.
Digital Solution Manager Location: Lisboa Time Type: Full time Job Description ZEISS is technology and innovation. Founded in Germany, in 1846, ZEISS is an internationally leading technology enterprise operating in the…
Oversees medical device software documentation and regulatory compliance for cardiovascular imaging tools, bridging clinical needs with engineering teams to ensure EU MDR/FDA submissions and post-market surveillance.
Build and own Aidoc’s QA strategy from scratch for regulated AI medical-imaging products, designing test architecture, automating with Python/pytest/Playwright, and integrating CI/CD to meet FDA/ISO standards.
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