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Our client, a leader in the healthcare industry, is seeking a Medical Device Test Engineer to join their team. As a Medical Device Test Engineer, you will be part of the Quality Assurance department supporting the testing and validation of medical devices used in invasive cardiology. The ideal candidate will demonstrate meticulous attention to detail, strong problem-solving skills, and a proactive approach to quality assurance, which will align successfully in the organization. Job Title: Medical Device Test Engineer Location: Waukesha, WI (Onsite) What's the Job? Design and execute manual test cases and scenarios for invasive cardiology medical devices Perform functional, integration, and system testing to ensure product quality Conduct verification & validation (V&V) activities for product releases Log, track, and validate defects to facilitate continuous improvement Prepare detailed test plans, reports, and validation documentation in...

Our client, a leading organization in the medical device industry, is seeking a Medical Device Design Quality Engineer to join their team. As a Medical Device Design Quality Engineer, you will be part of the Quality Assurance department supporting product development and manufacturing teams. The ideal candidate will demonstrate strong analytical skills, attention to detail, and a proactive mindset, which will align successfully in the organization. Job Title: Medical Device Design Quality Engineer Location: Pittsburgh, PA (Onsite) Pay Range:  $37-$42/Hr. on W2 What's the Job? Support design quality activities throughout new product development, including design reviews, requirements review, risk management, verification and validation planning, and design transfer readiness. Lead and participate in Design Failure Modes and Effects Analysis (DFMEA) and risk assessments to identify and mitigate design and manufacturing risks. Review protocols...

Job Title: Medical Writer II Part time - 20/Hours Per Week - 8am to 12pm Location: Little Canada, MN - 100% Onsite  Pay Range: $43 to $48/hr on W2  Job Details:  Author and update clinical evaluation documents, including Clinical Development Plans (CDPs), PMCF Plans, and Evaluation Reports, ensuring compliance with EU MDR requirements. Collaborate with clinical, risk evaluation, regulatory, and quality teams to develop high-quality, regulatory-compliant clinical evidence documentation. Review clinical evaluation documents for scientific and clinical accuracy, consistency, and data integrity. Support development of clinical study protocols, statistical analysis plans, and study reports as needed. Maintain thorough knowledge of supported products and interpret clinical data to inform benefit-risk assessments and regulatory submissions. What's Needed? Bachelor's degree in Science, Medical Technology, or a related field. Minimum of 3 years of...