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Manages the Quality Management System for medical device projects, ensuring ISO 13485:2016 compliance, design controls, and regulatory submissions while leading quality teams and audits.
Handles medical-device regulatory filings and compliance in India, including BIS certifications and health-authority communications, for a global medtech company.
Ensures flawless manufacturing and compliance of ophthalmic combination products by leading quality initiatives, risk management, and regulatory adherence in a GMP-regulated environment.
Quality Engineer validates and sustains manufacturing equipment, processes, and software for medical devices, ensuring FDA and ISO compliance while collaborating with cross-functional teams.
Validates and audits global suppliers for a medical device manufacturer to ensure compliance with ISO, FDA, and internal quality standards.
Oversee global regulatory compliance for medical devices, guiding teams to meet FDA, ISO, and EU MDR standards while ensuring safe, timely market access for clinical trial technologies.
Principal Supplier Quality Engineer at Medtronic drives supplier quality for new medical device development, ensuring components meet regulatory and clinical standards while collaborating with cross-functional teams and suppliers.
The Opportunity: Responsible for Smooth Functioning of plant & to meet monthly production with optimum utilization of resources of Plant & also responsible for research & development of Immunology - Rapid +…
At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We…
Leads quality engineering for orthopedic medical devices, applying risk management and regulatory compliance to new product development in a hybrid role.
Senior Engineer in Design Assurance at a medical device company, ensuring compliance with FDA and ISO standards by reviewing design requirements, risk management files, and validation protocols.
Join the team leading the next evolution of virtual care. At Teladoc Health, you are empowered to bring your true self to work while helping millions of people live their healthiest lives. Here you will be part of a…
Build and maintain automated test platforms for medical microrobotics, integrating mechanics, electronics, and software to verify and characterize brain-microrobot systems in a regulated lab environment.
Oversee quality systems, audits, and compliance in a regulated manufacturing environment to ensure products meet high standards and maintain certifications like ISO 13485.
Senior Quality Engineer at Medtronic in Humacao, Puerto Rico, ensuring medical device manufacturing meets strict regulatory standards like ISO 13485 and FDA QSR through quality systems, validation, and process improvements.
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in…
Oversee quality assurance for medical diagnostics in a regulated healthcare lab, ensuring compliance with ISO 13485, CMDR, and Health Canada standards.
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to…
Oversee and improve the quality of medical device components sourced from external suppliers, using audits, risk management, and corrective actions to ensure compliance with ISO 13485 and FDA regulations.
Designs and delivers technical learning programs for teams developing regulated medical device software, translating complex regulatory and engineering concepts into practical training for engineers and product managers.
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