- 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
- Takeda Pharmaceuticals (Lexington, MA)
- …to the best of my knowledge. **Job Description** **Senior Manager, US Medical Ad/Promo Regulatory Review** **Takeda Pharmaceutical** **Lexington, MA or Exton, PA** ... the role:** Join Takeda as a Senior Manager, US Medical Ad/Promo Regulatory Review where you will serve as...requirements and promotional strategy. + Mentor and help develop staff . Assist with training and sharing technical and regulatory… more
- Beth Israel Lahey Health (Chelsea, MA)
- …Word, Excel, Powerpoint or Access. **Preferred Qualifications** : 1. EMT, Paramedic, Certified Nursing Assistant or Medical Assistant training. 2. Urgent Care ... regulatory requirements. Performs, evaluates and documents Quality Control activities and device calibration. (essential) 2. Communicates lab results to members of… more
- Teradyne (North Reading, MA)
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... Engineering PMO with frequent direct interaction with the Engineering VP and staff . The position will work closely with Finance, Project Management, Planning, and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …our Lexington, MA or Exton, PA office. Where you will be working on the US Medical team, you will be empowered to serve as an internal expert on FDA regulations, ... relation to regulatory requirements and promotional strategy. + Mentor and develop staff . Supervise, train and provide technical and regulatory guidance to staff… 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