Medical Device Quality Supervisor Jobs (NOW HIRING)

Document production activities, lot traceability, and quality records per FDA and ISO regulations ... Identify and report non-conforming materials or process deviations to supervisors * Maintain a ...

Document production activities, lot traceability, and quality records per FDA and ISO regulations ... Identify and report non-conforming materials or process deviations to supervisors * Maintain a ...

Role: Medical Device Quality Engineer L ocation: Blue Ash, OH Duration: 6 months Role Descriptions: · 7+ years of engineering experience in medical device or other regulated industries. · ...

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience ... Demonstrate accuracy, thoroughness and monitors own work to ensure quality. * Practice and always ...

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience ... Demonstrate accuracy, thoroughness and monitors own work to ensure quality. * Practice and always ...

Minneapolis, MN Duration: Long Term Job Overview We are seeking a Quality Technician with experience in the medical device industry to support quality assurance activities, product investigations ...

You will bridge the gap between rapid Agile development and rigorous medical device regulations ... Design Quality & Risk Management * Technical Architecture Review: Advise on software architecture ...

You will bridge the gap between rapid Agile development and rigorous medical device regulations ... Design Quality & Risk Management * Design Reviews: Participate in software architecture reviews to ...

In this role, you'll help manufacture high-quality medical devices, including pacemakers ... Identify production issues and communicate concerns and potential solutions to supervisors and team ...

In this role, you'll help manufacture high-quality medical devices, including pacemakers ... Identify production issues and communicate concerns and potential solutions to supervisors and team ...

Ensure compliance with relevant FDA, ISO, EU MDR, global, and GSK requirements for medical devices ... Act as site Subject Matter Expert (SME) for device quality processes, providing guidance to ...

Follow detailed written instructions and assembly procedures to ensure product quality and accuracy ... supervisors Medical Device Assembler Qualifications/Requirements: * High school diploma or ...

Ensure compliance with relevant FDA, ISO, EU MDR, global, and GSK requirements for medical devices ... Act as site Subject Matter Expert (SME) for device quality processes, providing guidance to ...

Quality Assurance Engineer - Medical Devices Location: Northwest Minneapolis Metro Area Type: 6 ... a medical device environment. This role will partner cross-functionally to ensure compliance with ...

... medical device industry. Our customers view us as a trusted partner in the areas of injection ... The Supervisor leads a team of inspectors and technicians, providing clear direction ...

... medical device industry. Our customers view us as a trusted partner in the areas of injection ... The Supervisor leads a team of Quality Control personnel supporting New Product Introduction ...

Identify and communicate safety, quality, or process issues as needed * Maintain controlled ... Collaborate with supervisors, engineers, and technicians to resolve line issues and suggest ...

Quality Engineer - Medical Device Manufacturing Company Overview Flotec is an Indianapolis-based medical device manufacturer specializing in respiratory and oxygen delivery equipment. We manufacture ...

As the Senior Device Quality Engineering Lead, you will hold a pivotal role in ensuring the quality ... This senior-level position requires you to work closely with device development teams, medical ...

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience ... Demonstrate accuracy, thoroughness and monitors own work to ensure quality. * Practice and always ...