- Entrust (Shakopee, MN)
- …II** to join our team and take an active role in the design and development of Entrust Issuance solutions. The solutions are built using Java and modern Web ... to track progress and enforce project standards. + Knowledgeable about secure development life cycle, threat modelling, and web application security assessments. +… more
- Actalent (Minneapolis, MN)
- …This position requires a deep understanding of embedded systems engineering, medical device regulations, and the technical challenges associated with ... to enhance image quality. + Ensure adherence to stringent medical device quality systems through meticulous verification,...skills in C. + Knowledge of hardware and FPGA development . Additional Skills & Qualifications + Adaptability to pivot… more
- Abbott (Minnetonka, MN)
- …reporting gaps in manufacturing personnel training and knowledge Make sure all medical device operators are certified prior to performing manufacturing processes ... a full life. You'll also have access to: Career development with an international company where you can grow...of independent action and initiative Assist with interviewing of medical device candidates **Education** High School Diploma… more
- Fujifilm (St. Paul, MN)
- …manager, senior product manager, product/technical director). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience ... global R&D, operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with… more
- Philips (Plymouth, MN)
- …experience working in Regulatory Affairs and Quality/Quality Operations within the FDA regulated Medical Device industry, including 3+ years of experience and a ... Affairs and/or Quality teams. + You have extensive experience/knowledge of global medical device regulations, requirements, and standards (ISO 13485, ISO 14971,… more
- Philips (Plymouth, MN)
- …a minimum of 8+ years' Regulatory Affairs experience within FDA regulated Medical Device /HealthTech product environments. Experience with Software as Medical ... will lead and provide regulatory oversight for critical new product development projects, ensuring our state-of-the-art Ultrasound Products meet FDA, and other… more
- Abbott (Plymouth, MN)
- …environmental monitoring and that microbiology requirements are considered in product and process development activities. + Support all Divisional initiatives as ... a broader enterprise/cross-division business unit model preferred. + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn… more
- Cognizant (St. Paul, MN)
- …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... paper Batch record and business process flow in collaboration with business SMEs Data-driven, user-centric,...of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute… more
- Abbott (Plymouth, MN)
- …for Abbott's Electrophysiology business unit + Engage with development (Research and Development and Process Development ) teams to build knowledge for ... Minimum 5 years manufacturing engineering experience. Prior manufacturing engineering or process development experience is required. + Strong analytical, problem… more
- Abbott (Minnetonka, MN)
- …environmental monitoring and that microbiology requirements are considered in product and process development activities + Support all Company initiatives as ... **What You'll Work On** + Identify and implement effective process control systems to support the development ,...well as attention to detail **Preferred Qualifications** + Prior medical device experience preferred + Experience working… more