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Overview: Ensures compliance with applicable standards and regulatory requirements (e.g., FDA, ISO) Leads laboratory-based quality activities, including hand on experience with Test Method Validation (TMV), Design…
A Career at Clarius Today, as many as 25 million medical professionals globally don’t have access to medical imaging, which is proven to improve patient care and reduce healthcare costs. That’s why we’re on a mission…
Design and optimize Snowflake-based data platforms for a medical device company, ensuring compliance with healthcare regulations and enabling analytics and AI/ML use cases.
jerryJob Description Field Service Technician – Canada Remote Position, Field Based – Greater Toronto Area Hourly Rate: $38.00 -$55.00 CAD per hour, commensurate with experience Summary The primary responsibility of…
Job Summary The Quality Engineer leads and uses Quality & Process Engineering principles, tools and practices to develop and optimize systems, and ensure processes are aligned with the overall business and quality…
This role provides supply chain and test engineering expertise for medical device products, managing electronic component sourcing and developing automated test platforms using LabVIEW, SQL, and other languages. The position involves strategic oversight of hardware and software test systems, supplier management, and ensuring regulatory compliance in a medical device environment.
Technical Service Operations Manager StemWave | Full-time, On-site | $90,000 – $125,000 depending on experience About the Role: StemWave is scaling from one product line to three over the next 18 months. We're…
Primary Function of the Position The Post Market team at Intuitive works at the intersection of Regulatory and Quality. The team engages across the organization to deeply understand how our products and processes…
About Meridian Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and…
Overview Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our…
In This Position, You Will Have the Opportunity To Prepare and submit regulatory filings for U.S. and international markets, including 510(k)s, STED files, Design Dossiers, and Rest-of-World documentation, under the…
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Principal National Support Engineer II based in the United States. This is a senior Tier…
his position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Device Regulatory CMC - Manager based in United States. This contract role supports…
As part of our continued growth, we are looking to recruit technical and experienced Medical Device Assessors/Lead Auditors. The successful candidates will be responsible for planning and conducting audits /…
As the Associate Production Engineer, you will be the technical lead for the assembly and delivery of our precision robotic prostate biopsy systems. As part of the link between R&D, the manufacturing line, and the…
Software Product Owner managing the product backlog for a medical device software product, bridging clinical stakeholders and engineering teams using Agile/Scrum, with QMS and regulated documentation responsibilities.
Job Summary Develops, applies and maintains quality requirements and standards for manufacturing products and testing. · Design and implement methods for process control, process improvement, testing and inspection ·…
Job Summary Lead and manage production operations to ensure safety, quality, delivery, and productivity targets are achieved while maintaining compliance with ISO 13485, FDA, and company standards. Key Responsibilities…
Senior QA Engineer ensuring FDA/ISO 13485 compliance for medical device manufacturing—managing CAPA, audits, validations (IQ/OQ/PQ), root cause analysis, and quality documentation.
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