- Bausch + Lomb (Bridgewater, NJ)
- …relating to submissions and regulatory approval of medical devices. Knowledge of medical device product labeling processes for review and obtaining ... and external standards meetings with Quality and cross- functional teams for labeling requirement visibility. + Monitors, evaluates and recommends improvements… more
- Amgen (Washington, DC)
- …pharmaceuticals, natural science or medicine + Experience in Pharmaceutical, Biotechnology and/or Medical Device industry and product labeling + Experience ... for a career you can be proud of. **Global Labeling Strategy Sr. Manager - TA Head** **Live** **What...Organizational expert within defined subject area + Experience in Medical Device industry, including Design Controls and… more
- West Pharmaceutical Services (Exton, PA)
- …support submissions including Premarket Notifications, Technical Documentations under EU MDR ( Medical Device Regulation), and Master Files (DMF/MAF) associated ... leadership skills, as well as demonstrated understanding of pharmaceutical and/or medical device operations (eg, manufacturing, process development, analytical,… more
- Abbott (Alameda, CA)
- …+ Ensure that electrical design and test equipment meet applicable industry and medical device standards. + Specify, design, verify and validate, sustain very ... Electrical Engineering principles. + Solid knowledge of regulations and industry standards for medical device development and in vitro diagnostic device … more
- Terumo Medical Corporation (Phoenix, AZ)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $5+ billion in sales, 20,000+ employees worldwide ... Systems and Terumo Medical Products. **Job Summary** As a regulated medical device organization our Inventory Cycle Counter are critical to the… more
- Medtronic (Minneapolis, MN)
- …manufacturing and design changes + Experience with FDA requirements, guidance documents, Medical Device Directive, ISO 14971, ISO 13485, and other global ... worldwide regulatory affairs support for Class II and Class III medical devices including combination products. The Regulatory Affairs Specialist is responsible… more
- Veterans Affairs, Veterans Health Administration (Amarillo, TX)
- …Verbalizes and demonstrates process for obtaining lab specimens, proper labeling and immediate transport. Recognizes and responds to impaired airway-notifying ... onboarding process. Participation in the seasonal influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP).… more
- Edwards Lifesciences (Irvine, CA)
- …4 years experience related experience Required and HS Diploma or equivalent medical device assembly Preferred Associate Degree Preferred **What else we ... inventory to ensure appropriate storage conditions, movement and correct labeling of product status * Providing coaching and training...of procedures * Proficient in all inspection techniques for medical device product inspection * Ability to… more
- Takeda Pharmaceuticals (Lexington, MA)
- …packaging design qualification. + Provide technical expertise for developing packaging/ labeling material selection, qualification, and process implementation for new ... all aspects of a packaging project delivering early phase evaluation to the device sub-team. Deliver on specific performance indicators, including but not limited to… more
- WellSpan Health (Chambersburg, PA)
- …sharps safety, no pass zone, PPE protection in the surgical areas, medication labeling and specimen handling. 18. Is cognizant and monitors SCIPS information as it ... cardiac arrests codes as a team member. - For Device Clinic, at least one year of device...For Family Birthing position posted as a trainee position, requirement of at least 1 year of experience as… more