- Terumo Aortic (Sunrise, FL)
- …can develop their skills and achieve career goals. Working for the company, each associate 's role contributes greatly to helping to save or improve the lives of ... degree in engineering/science and a minimum of 5 years' experience in the medical device industry or master's degree in engineering/science and a minimum of 4 years'… more
- Amgen (New Albany, OH)
- …the provision of **technical operations support** for the **continuous improvement** of device assembly and packaging line capacity and performance, and advisory of ... as the site technical expert for automated and semi-automated device assembly for FDP and non-combination **products** . Be...years of working in a GMP regulated environment Or Associate 's degree and 8 years of working in a… more
- GE HealthCare (Troy, NY)
- …throughput + Lead and support documentation activities related to medical device manufacturing, ensuring compliance with regulatory requirements + Develop and ... in collaboration with the engineering team + Coordinate process flow for Device History Records (DHRs), manage data within electronic record systems, and oversee… more
- Bausch + Lomb (Clearwater, FL)
- …correction implants. The Precision Machinist ensures compliance with stringent medical device industry standards and works closely with engineering, quality, and ... comply with Current Good Manufacturing Practices (cGMP) and relevant medical device regulations. + Ensure compliance with good documentation practices. + Oversee… more
- Integra LifeSciences (Columbia, MD)
- …engineering leadership within the constraints of domestic and foreign Medical Device Regulations. The employee will investigate, determine root cause, and implement ... engineering disciplines. + Demonstrates ability and initiative to mentor Associate / Staff engineers **Additional Responsibilities** + Participate in design… more
- Integra LifeSciences (Plainsboro, NJ)
- …overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be ... knowledge, skill, and/or ability required for this position. + Associate degree in science is preferred. + 3-7 years...in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical … more
- Terumo Neuro (Aliso Viejo, CA)
- …Description:** Support and lead teams in the development of medical device products, including writing or verifying specifications; maintaining product process; ... property; write invention disclosures. + Supervise technicians, specialists, and associate engineers. + Specify and/or direct the specification and testing… more
- Nissha Medical Technologies (Buffalo, NY)
- …(NPI) will lead the successful onboarding and ramp-up of new medical device programs within a contract manufacturing environment. This role is critical in ... design to Nissha's manufacturing floor, including development of DMRs ( Device Master Records) and DHFs (Design History Files). +...time to recharge. Paid time off is an essential associate benefit and a pillar of self-care. + Engagement… more
- ZOLL Medical Corporation (Atlanta, GA)
- …offerings.ZOLL Itamar is a division of ZOLL Medical and an established medical device company focused on the development, manufacturing, marketing and sales of sleep ... range of customer sales agreements (eg, customer sales agreements for medical device , related services, SaaS and software licensing; service level agreements, ASP… more
- Guthrie (Sayre, PA)
- …Microsoft operating system end‐user computing Gold Image, including all necessary device drivers and enterprise software. + Experience in Windows scripting ... and managing policies and software packages. + Experience with mobile device management. + Basic understanding of LAN/WAN network infrastructure technologies. +… more