- US Tech Solutions (San Bruno, CA)
- …Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation ... and support CAPA, complaints, audits, and overall QMS functions. **Experience:** ** Medical Device Software Experience:** 1. Proven experience in software… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... replacement of various types of facilities infrastructure in support of a medical device cleanroom manufacturing facility. The primary responsibility is to… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Japanese Pharmaceutical Affairs Laws, the Canadian Quality System Regulation, and the Medical Device Directive. **Job Details/Responsibilities** + Manage a team… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... replacement of various types of facilities infrastructure in support of a medical device cleanroom manufacturing facility. The primary responsibility is to… more
- Stryker (Oklahoma City, OK)
- …Degree in nursing or clinical required + Minimum of three (3) years; in medical device clinical capacity or cath lab. + Proven understanding of cardiovascular ... in increased clinical acumen. Responsibilities: + Educate physicians on device handling, implantation and troubleshooting techniques related to Inari products.… more
- Cook Medical (Bloomington, IN)
- …position provide s real-world experience with meaningful projects in the medical device manufacturing industry. Responsibilities - Utilize engineering knowledge ... to p roduce project deliverables / documents - Adhere to the Quality Management System (QMS) and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements - Must maintain all training requirements for the position, while… more
- Cook Medical (Bloomington, IN)
- …internships provide hands-on experience with meaningful projects in the Medical Device Manufacturing Industry. Responsibilities Responsibilities/projects may ... include: + Involvement with a product launch + Data gathering and analysis. + Use of Artificial Intelligence (AI) + Identify and recommend product growth opportunities + Identify and recommend margin growth opportunities + Identify and recommend competitive… more
- Globus Medical, Inc. (Methuen, MA)
- …electrical engineering principles, ensuring robust hardware solutions and compliance with medical device standards while driving innovation in product ... + Foster a culture of innovation, collaboration, accountability and compliance with medical device standards. Ensure timely delivery of milestones within budget… more
- Globus Medical, Inc. (Limerick, PA)
- …fixed burrs, cleaning of sharp edges, and polishing and blending machined surfaces of the medical device (s). The job requires the individual to be a team player ... of sharp edges, and polishing and blending machined surfaces of the medical device (s). * **Assembler I:** entry level role, deburring of components, such as… more
- Lilly (Indianapolis, IN)
- …execution and reporting of design and human factors activities across all medical device , combination product and packaging programs, according to current ... regulations and appropriate guidelines within the medical device and biopharmaceutical industries. **Position responsibilities** : **Design and Human Factors:**… more