- Teleflex (Morrisville, NC)
- …market releases. **Principal Responsibilities** 1. Designs, develops, verifies, and maintains medical device software following industry best practices, ensuring ... with all layers of full-stack development and verification of medical devices , while ensuring compliance with all...aviation). **Specialized Skills / Other Requirements** * Experience with medical device regulatory standards such as 21… more
- Medtronic (Plymouth, MN)
- …or a related field + Experience in a Class II medical device industry + Experience with design or manufacturing process development and validation ... leader to design, develop and provide technical expertise in post-market released medical devices . Lead released product engineering teams through planning,… more
- Snap Inc. (Palo Alto, CA)
- …that validate device posture, health, and identity, ensuring only trusted devices can access internal and SaaS applications + Secure corporate and SaaS ... and always execute with privacy at the forefront. We're looking for a Security Engineer to join our Enterprise Infrastructure Security (EIS) team! What you'll do: +… more
- Terumo Neuro (Aliso Viejo, CA)
- …Knowledge of standard machine shop equipment and processes, and working knowledge of medical device manufacturing equipment and processes. 5. Computer ... Quality + Supply Chain Job duties: Support development of medical device products with work including writing...Zero (0) to two (2) years of experience in medical devices , manufacturing and/or technical… more
- Stratasys (Eden Prairie, MN)
- … industry experience **PREFERRED QUALIFICATIONS:** + Preferred experience with medical manufacturing process requirements, designing and implementing tools ... Senior Medical Segment Applications Engineer Location: Eden...a team, with multiple departments + Experience in the medical device and component industry **TRAVEL REQUIREMENT:… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …Assurance, Quality Control, or Product/Process non-conformance investigations + Experience in a medical device or pharmaceutical manufacturing facility. + ... **Job Description Summary** The Quality Engineer II is responsible for the application and...required. Familiarity with Design Control requirements and knowledge of Medical Device Validations is preferred. **Education and… more
- Medtronic (Jacksonville, FL)
- …or Biomedical Engineering; and five (5) years of experience as a mechanical design engineer for medical devices or related occupation. Must possess at ... and Quality control of Class II and Class III medical devices including capital powered equipment and...Regulations (QSR) 21 CFR 820, ISO13485, ISO14971, and EU Medical Device Directive (MDD)/ Medical … more
- AbbVie (Worcester, MA)
- …21 CFR Part 11 requirements for automated systems in the pharmaceutical or medical device industries. + Demonstrated problem solving skills and innovative ... Automation Engineer will ensure the success of Drug product manufacturing through an extensive understanding and solid background in engineering, configuration,… more
- VTI Life Sciences (Naples, FL)
- …and process validation protocols (IQ, OQ, PQ) and reports for equipment used for manufacturing medical devices such as metal instruments/ implants, ABS/Peek ... Validation Engineer /Consultant for our Naples, Florida area medical device client to lead and coordinate...instruments/implants. + Execute validation protocols for manufacturing equipment such as Laser marking, Laser welding, Passivation,… more
- Northrop Grumman (Linthicum Heights, MD)
- …in semiconductor/microelectronics packaging for space, defense, or medical devices . + Knowledge of mechanical manufacturing and production processes. ... insight to integrate these processes into robust, repeatable, and cost-effective manufacturing flows. The Senior Principal Engineer will provide technical… more