- Terumo Medical Corporation (Elkton, MD)
- …or similar. + Requires six to ten years increasing responsibility and experience in a medical device quality assurance environment. + Prefer one to two years ... develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- 3M (Maplewood, MN)
- …Here, you will make an impact by: + Leading the development and implementation of global Medical Device Quality Processes for 3M + Leading Global Quality ... or military environment + Two (2) years of experience in Quality System in Medical Device regulated environment. Additional qualifications that could help… more
- Hologic (Marlborough, MA)
- … data evaluation. + Awareness of industry advancements and best practices in medical device quality management. **Skills** + Exceptional leadership and ... Sr. Manager Post Market Quality Newark, DE, United States Marlborough, MA, United...customer success, apply today! **Knowledge** + Strong understanding of Medical Device Regulations, including FDA requirements (21… more
- Philips (New Kensington, PA)
- …fit if:** + You have a minimum of 5+ years' experience within FDA regulated medical device Quality environments, with a focus on CAPA reviews, ... The Senior Quality Engineer-CAPA will play a critical role within...opportunities for improvement. + You have detailed knowledge of medical device regulations, requirements, and standards, such… more
- ManpowerGroup (Westford, MA)
- …Westford, MA **Pay Range: $45/hr on w2** **What's the Job?** + Initiate and oversee medical device quality assurance activities in compliance with FDA ... Our client, a leader in the medical device industry, is seeking a Quality Engineer to join their team. As a Quality Engineer, you will be part of the… more
- GE HealthCare (Waukesha, WI)
- …in the medical device field. + Demonstrated understanding of Medical Device Quality Management System requirements and regulatory requirements ... **Job Description Summary** Responsible for QA activities in support of medical device history record review, final acceptance and final product release. Ensures… more
- J&J Family of Companies (Palm Beach Gardens, FL)
- …or Digital Platforms + A minimum of 5 years' experience in managing FDA and ISO Medical Device Quality and facility inspections. + Proven record of relating ... and audit support functions. + Provide leadership in the understanding of medical device regulations to other disciplines. + Communicate effectively at… more
- Terumo Neuro (Aliso Viejo, CA)
- …validation and data analysis. 3. Demonstrated command and knowledge of FDA and ISO medical device quality system requirements. 4. Proven experience in ... quality engineering projects to support the manufacturing of medical devices. Work with Manufacturing and R&D in leading...design verification, and design validation. 2. Strong knowledge of medical device design control process. 3. Ability… more
- System One (Lakewood, CO)
- …may have a Master of Science degree in Engineering, preferred. + Minimum 10 years' global medical device quality experience, five (5) of which have been in a ... relocation assistance Type: Direct/Permanent Start date: Immediate Overview: Our client, a global medical device company, is seeking a Senior Manager, Supplier … more
- Medtronic (Jacksonville, FL)
- …policies and Standard Operating Procedures (SOPs) to ensure that FDA, ISO and European Medical Device quality standards and regulations are met where ... **A Day in the Life** **Prin** **.** **Software** **Design** ** Quality Engineer** Medtronic ENT (Ear, Nose, and Throat) is...**on your resume.** **Nice to Have** + Experience with medical device design controls, embedded devices, hardware… more
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