- Lilly (Indianapolis, IN)
- …development. **Additional Preferences and Information:** + Knowledge of cGMP requirements in medical device manufacturing, highly preferred. + Experience in ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to… more
- ThermoFisher Scientific (Middletown, VA)
- …VA Specialty Diagnostics Group (SDG) **How will you make an impact?** The Medical Device Complaint Handling Specialist III is responsible for managing and ... + Detailed knowledge of ISO 13485 and GMP regulations which govern a medical device and diagnostics manufacturing. + Strong analytical and problem-solving skills… more
- Medtronic (Billerica, MA)
- …and writing in English. **Preferred Qualifications (Must Have!):** + Prior experience in the medical device or electronics industry. + Knowledge of ISO and FDA ... life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with...up to 6% match + Comprehensive benefits plan, including medical , dental, vision, and more + Fully subsidized Bachelors… more
- Lilly (Indianapolis, IN)
- …members and the Original Equipment Manufacturers (OEM) to design and build custom medical device assembly machines. These engineers also develop and implement ... for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around...make life better for people around the world. Indy Device Manufacturing (IDM) is an external facing team responsible… more
- Ricoh Americas Corporation (Indianapolis, IN)
- …in a technical field and 3+ years of experience in manufacturing quality operations medical device industry. + ISO 13485 experience required + Experience working ... quality responsibilities and documentation for the Ricoh 3D Printing for Healthcare covering production related quality activity for multiple sites. This position… more
- Fujifilm (Bothell, WA)
- …project plan through leadership of the with cross-functional project team and in compliance with QSR820.1 (FDA medical device ) requirements. + Build ... areas of product definition, project strategy and resource deployment. Ensures compliance with established procedures for product development in a regulated… more
- dsm-firmenich (Exton, PA)
- …equivalent years of experience in related fields. + 0-5 years' experience, preferably in Medical Device manufacturing or GMP related industry. + Ability to work ... 18 days PTO + 2 floating holidays. + Full healthcare benefits day one - medical , dental,...experience working with machinery, tooling, and products/processes in a medical device environment preferred. + Industrial scale… more
- RWJBarnabas Health (Newark, NJ)
- Director Patient Care Ventricular Assistive Device (VAD) ProgramReq #:0000189067 Category:Professional / Management Status:Full-Time Shift:Day Facility:Newark Beth ... Israel Medical Center Department:Cardiac Recovery Room Pay Range:$125,000.00 - $175,000.00...NJ 07112-2027 Job Title: Director Patient Care Ventricular Assistive Device (VAD) Program Location: Newark Beth Israel Med Ctr… more
- Merck (Rahway, NJ)
- …Factor Engineering, Inventory Control System, Inventory Management, Mechanical Testing, Medical Device Quality Systems, Negotiation, Project Management, Quality ... applicable. We offer a comprehensive package of benefits. Available benefits include medical , dental, vision healthcare and other insurance benefits (for… more
- Medtronic (Newton, MA)
- …and debugging software that interfaces with hardware components. Experience with regulatory compliance and security protocols specific to medical software (eg, ... life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with...that enhance the usability and functionality of our advanced medical devices. The Senior Software Engineer will be a… more