- Integra LifeSciences (Boston, MA)
- …and years of experience. + Min. 5-7 years' direct QE experience in a regulated med device , life sciences or pharma industry with direct experience in dFMEA and ... patient outcomes and set new standards of care. The Staff Quality Engineer is a subject matter expert responsible...of statistical sampling and analysis. + Working knowledge of medical device regulations (including FDA QSRs, ISO13485).… more
- Integra LifeSciences (Mansfield, MA)
- …will provide technical expertise and project management in the areas of medical device manufacturing process development and validation, DFM, COGs management, ... and Manufacturing to develop and improve surgical products for the neurosurgical medical device industry. * Recognized manufacturing process technical expert who… more
- Robert Half Technology (Worcester, MA)
- …of technology across the organization. A strong understanding of MacOS, mobile device management (MDM), and inTune/Jamf is essential for success. Responsibilities: + ... + Scripting (PowerShell, VB, VBScript, Batch, etc.) + Training technical and non-technical staff and customers on IT use + Documenting standard support procedures +… more
- Philips (Boston, MA)
- …work/military experience. + Your skills include + Extensive knowledge of the medical device industry and associated product portfolios, preferably within ... and support - including new program launches, physician and staff training. **You're the right fit if:** + You...right fit if:** + You are a **Registered or Certified Cardiac Sonographer (RCS) or a Registered Diagnostic Cardiac… more
- Takeda Pharmaceuticals (Boston, MA)
- …standard for good clinical practice, compliance, and ethics. + Mentors junior staff to promote scientific excellence and individual achievement. + Participates as a ... Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/ Device , and Global Regulatory Affairs. + Advanced knowledge of… more