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Job Title Senior Quality Operations Manager-Advanced Imaging Job Description The Senior Quality Operations Manager is responsible for overseeing strategic process validation initiatives, driving targeted/continuous…
Senior Software Architect leading architecture for robotic procedure automation software—UI, clinical workflows, and hardware/software integration—using C++ within a regulated medical-device environment at Philips.
Lead the architecture, governance, and technical strategy of a controlled AI/LLM Harness platform for medical-device R&D, ensuring compliance with quality-system regulations using RAG, prompt governance, and enterprise AI platforms.
Manages the sterility assurance program in a GMP-regulated manufacturing environment, overseeing sterilization validations, aseptic process simulations, contamination control, and compliance with FDA, EMA, and EU GMP Annex 1 standards.
Working at Freudenberg: We will wow your world! Responsibilities: Ensure all customer requirements are identified, clearly documented in Freudenberg Medical manufacturing documentation and effectively implemented.…
Company: Mitsubishi Chemical Advanced Materials Inc. Job Description: About the Role Are you ready to take your quality expertise to the next level? As a Quality Engineer III , you’ll be a senior leader driving…
At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries…
The QA Auditor manages internal, supplier, and customer audits to ensure compliance with cGMP and regulatory standards. The role involves coordinating CAPA processes and supporting regulatory inspections across multiple facility sites.
The Senior Quality Assurance Engineer manages internal and supplier audit programs to ensure regulatory compliance for medical device manufacturing. The role involves mentoring auditors, coordinating CAPA investigations, and preparing for external audits using quality management standards like ISO 13485.


 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…
This Quality Assurance Engineer role at Becton Dickinson involves managing inspection criteria, conducting process validations (IQ/OQ/PQ), and ensuring cGMP compliance within a medical device manufacturing environment. The position requires statistical analysis skills and bilingual proficiency in English and Spanish to support quality investigations and audits.
About Us: How many companies can say they have been in business for over 178 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the ever-changing environments in a fast-paced world,…
Staff Design Quality Engineer at Stryker in Portage, MI, ensuring medical device designs meet safety, cybersecurity, and regulatory standards while partnering with R&D, operations, and suppliers.
Ensures compliance and quality in medical device development/manufacturing by leading QA processes, risk management, audits, and CAPA investigations across cross-functional teams.
California, US residents click here. The job details are as follows: Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit…
Are you passionate about ensuring the quality and reliability of life-saving medical devices? At Hologic, we are seeking a Product Quality Engineer 2 to provide engineering support for on-market medical devices. In…
ABOUT CWT: Custom Wire Technologies (CWT) is a leading OEM medical component manufacturer, with over 50 years of industry experience and implementation of the latest technology. Our services include custom wire…
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we…
Manages and improves medical-device design control processes, ensuring FDA/ISO compliance, translating regulatory requirements into actionable procedures, and driving adoption across R&D and product teams.
Oversees technical quality for wound care products, ensuring compliance and safety via validation, equipment qualification, and risk management in a regulated medical device environment.
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