- Albany Medical Center (Albany, NY)
- …course of the study a. 1572 (pharmaceutical trials) b. Statement of investigator ( device trials) c. Financial Disclosure forms for PI and Sub Investigators (SI) d. ... CV and medical license for PI and Sub Investigators (SI) e....administer study medication injection. 16. Review oral study medication compliance with patient at each visit 17. Collect required… more
- Meta (New York, NY)
- … compliance team. You will get to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals.You will work on ... discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. Experience working with… more
- Stryker (Memphis, TN)
- …and dependencies. + Experience validating finished good data in the medical device industry. + Familiarity with GMP/GDP compliance and QMS processes. + Basic ... shape the strategic vision for product master data management, ensuring accuracy, compliance , and alignment with Stryker's global strategy. Your work will enable a… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …including direct experience in clinical investigation and 6 years' experience in the Medical Device /In Vitro Diagnostics or related industry **OR** a Bachelor's ... Procedures to optimize MA functioning in terms of leadership, compliance and productivity. The Director, Medical Affairs,...Degree in Nursing and 10 years' experience in the Medical Device /In Vitro Diagnostics or related industry… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …suffering from serious cardiopulmonary and respiratory conditions.ZOLL Itamar is an innovative medical device technology company that focuses on the development ... of field sales experience - client focus within cardiology, medical device and/or pharma industries + Two...protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of… more
- Oracle (Baton Rouge, LA)
- …and scalable processes. + Serve as the escalation authority for device performance, software/firmware issues, and field incidents. + Author roadmaps, investment ... cases, automation strategies, and device standardization documents. **KEY RESPONSIBILITIES:** + Develop, communicate, and...deliver against project milestones and SLAs, ensuring performance and compliance at every stage. + Drive adoption of IoT… more
- West Pharmaceutical Services (Exton, PA)
- …regulatory requests. **Essential Duties and Responsibilities** + Develop and implement medical device regulatory strategies for West's Transfer Devices with ... Experience: Bachelor's with 5+ years; Master's degree/PhD with 3+ years of medical device , pharmaceutical or regulatory experience **Work Experience** +… more
- AbbVie (Irvine, CA)
- …in vivo and tissue processing methods to support development of novel medical device /tissue products. + Critically evaluate scientific or regulatory advances, ... (cell biology, molecular biology, pharmacology, immunology, bioengineering, or similar) + Medical device experience or experience in a regulated environment… more
- Hologic (Boston, MA)
- …ensures the highest standards of service delivery for medical device products, driving customer satisfaction, regulatory compliance , and operational ... + Oversee installation, preventive maintenance, troubleshooting, and repair of medical devices across hospitals, clinics, and healthcare facilities in ME,… more
- Terumo Medical Corporation (Boston, MA)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... demonstrating understanding of sales processes, effective targeting and operational compliance . + Ensure to the best of their ability...Prior experience as a Field Clinical Specialist with a medical device company is preferred. + Prior… more