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Our client is one of the leading players in the medical devices manufacturing sector. Due to their current expansion plan, they are looking for a multiple headcounts of Senior/Quality Engineer to join their team, in…
QC Specialist responsible for leading non-conformance resolution, monitoring QC lab performance, driving process improvements, and ensuring ISO 13485/MDSAP regulatory compliance in a regulated medical technology manufacturing environment.
Are you an experienced manufacturing leader with a strong track record in regulated production environments ? This is an exciting opportunity to take ownership of production operations, drive operational excellence,…
Who we are You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: Welcome to our…
Salary: Up to $5,000/month Employment Type: Permanent Working Hours: Office Hours Job Scope: Lead laboratory operations and supervise Lab Analysts and Technicians Review analytical results, investigate quality issues,…
Provide engineering support for manufacturing operations, focusing on process optimisation, equipment reliability, productivity and OEE improvement. Lead automation, equipment upgrade and assembly improvement projects,…
Responsibilities: Lead product quality initiatives for the assigned tester product line, including quality planning, project schedule management, implementation, and effectiveness verification. Analyze the root causes…
The Senior Quality Assurance Executive will manage quality systems, design controls, and regulatory documentation for molecular diagnostics and genomics products. This role involves working closely with R&D and production teams to ensure compliance with ISO 13485, ISO 14971, and regulatory standards like HSA and EU IVDR.
The Quality Control Engineer shall be the leader or accountable for the following Quality Control activities on “NPI handed over / Mass Production lines “. Quality Inspection: Effective Sampling on visual inspections…
Program Manager leading enterprise software development programs for regulated medical device products, coordinating cross-functional teams through the full SDLC, cloud and on-prem deployments, and compliance with FDA/ISO standards.
Lead embedded software engineer designing and developing C/C++ applications and algorithms (signal processing, real-time control, sensor fusion/tracking) for medical devices.
McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable.…
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work…
Build a career powered by innovations that matter! At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing—improving productivity, enhancing people’s lives and…
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet…


 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…
We anticipate the application window for this opening will close on - 11 Sep 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore…
Senior Design Quality Engineer leading design quality, reliability studies, risk management, and verification/validation for neurovascular medical devices at Medtronic, partnering with R&D through the full product development lifecycle.
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