- Takeda Pharmaceuticals (Cambridge, MA)
- …teams and the compliance committee, guiding the development of commercial and medical strategies and helping the teams manage and mitigate legal risk. + Advising ... the US Compliance Committee. + Working collaboratively across functions, including Compliance , Regulatory and Medical Affairs, to support a policy, training… more
- Abbott (Santa Clara, CA)
- …Summary** Responsible for Biocompatibility support to the research & development of new medical device products as well as the maintenance of business activities ... products to meet the existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO 10993 series. **Principal… more
- Abbott (Plymouth, MN)
- …support processes. In this role, you will also be responsible for performing medical device regulatory reporting in accordance with global regulatory guidelines, ... authorities. **What You'll Work On** + Independently determining and filing appropriate medical device regulatory reports with various regulatory agencies and… more
- Arizona Public Service (Phoenix, AZ)
- …to E-Verify poster. View the employee rights and responsibilities under the Family and Medical Leave Act (FMLA). In compliance with the Drug Free Workplace Act ... Protection provides critical support for APS's NERC PRC and CIP compliance programs through high-volume, accuracy-critical data entry, workflow management, and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …communication skills are required. + Demonstrated ability to facilitate the interface with medical device vendors and HF consulting firms. + Demonstrated ability ... Your Rights' (https://www.eeoc.gov/employers/eeo-law-poster) poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT (http://www.dol.gov/whd/regs/ compliance /posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND MEDICAL… more
- Hologic (Marlborough, MA)
- …and maintaining robust CI/CD infrastructure and development tools to support high-quality medical device software delivery. This role requires you to bridge ... systems, especially SVN and Git, including migration strategies. + Familiarity with medical device software development standards and regulatory frameworks (eg,… more
- Mount Sinai Health System (New York, NY)
- …This position ensures consistent supply charging practices across departments and facilities, compliance with clinical research and free device set-ups, and the ... processes, and workflows to ensure timely, accurate and compliant recording of hospital device -related revenue and maintenance of the CDM for all Mount Sinai Health… more
- BD (Becton, Dickinson and Company) (Warwick, RI)
- …with appropriate level of experience. + Minimum 1-2 years Regulatory Affairs experience in medical device or in vitro diagnostic device companies. + Proven ... focus, cross-functional collaboration and teamwork skills. + Working knowledge of US medical device regulations, 21 CFR 820 Quality System Regulation, and… more
- PCI Pharma Services (Bedford, NH)
- …and Controls, Utilities, Facilities, and Maintenance in supporting pharmaceutical and medical device product manufacturing across the PCI Manchester and ... of utilities and facilities supporting aseptic operations and non-aseptic medical device manufacturing activities across multiple plants. Additionally… more
- Penn Medicine (Bryn Mawr, PA)
- …leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across ... day. Are you living your life's work? **Looking for a FT Medical Esthetician** Summary: Responsible for cosmetic skin services, customer satisfaction, and product… more