- Veterans Affairs, Veterans Health Administration (New Orleans, LA)
- …and procedures from organizations such as the Food and Drug Administration ( FDA ), Association for the Advancement of Medical Instrumentation (AAMI), Joint Commission ... (JC), International Association for Healthcare Central Service Materiel Management (IAHCSMM), Association of periOperative Nurses (AORN), and others; Working closely with Supply Chain Management to monitor inventory levels to identify and take corrective… more
- University of Utah (Salt Lake City, UT)
- …and experience in human subjects research. Must have a working knowledge of FDA , ICH , and other regulatory compliance; an understanding of medical terminology ... and technical writing experience. Excellent interpersonal communication (including oral and written) and leadership skills also required. Must be proficient in Microsoft Office and possess the ability to learn new software programs. This position is… more
- Medtronic (Lafayette, CO)
- …filings in the US and EU. Directly engage with regulatory bodies (eg, FDA , Notified Body) to negotiate approvals and resolve complex regulatory issues. **Team ... Leadership & Development:** Direct the allocation of resources to a portfolio of product programs, ensuring alignment with corporate priorities and maximizing return on investment. Make key decisions on team structure, talent acquisition, and professional… more
- Bristol Myers Squibb (Devens, MA)
- …with 1+ year of manufacturing site experience. + Experience in FDA /EMA regulations in biopharmaceuticals or cell therapy manufacturing. **BMSCART** **\#LI-ONSITE** ... **GPS_2025** If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Compensation Overview:** Devens - MA -… more
- UPMC (Pittsburgh, PA)
- …ensuring full compliance with DEA and all regulatory agencies (JCAHO, PA DOH, FDA , USP, OSHA). + Lead daily pharmacy operations for centralized and decentralized ... areas, ensuring safe, accurate, and timely medication services through effective staff supervision and workflow coordination. + Manage recruitment, orientation, performance evaluation, and ongoing staff development, including competency training, coaching, and… more
- Arvinas (New Haven, CT)
- …mutations. On August 8 th 2025, the US Food and Drug Administration ( FDA ) accepted the New Drug Application (NDA) for vepdegestrant- an investigational, orally ... bioavailable PROTAC estrogen receptor degrader- for its use as a monotherapy in the treatment of adults with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-), ESR1-mutated advanced or metastatic breast cancer… more
- HCA Healthcare (Chattanooga, TN)
- …Principal Investigator. Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as ICH Good Clinical Practices and IRB requirements. ... Promote organization to private industry or governmental sponsors of clinical trials. Assists in preparing study contracts and budgets. Obtain detailed knowledge of all components of study protocol through independent analysis and review of study to complete… more
- Curia (Albuquerque, NM)
- …+ High school diploma or general education degree (GED) + FDA manufacturing regulated industry experience in an aseptic manufacturing environment, preferred ... + Operations or quality assurance in any industry, preferred Other Qualifications: + Must pass a background check + Must pass a drug screen + May be required to pass Occupational Health Screening + Must pass pre-employment assessment + Must be able to obtain… more
- ICON Clinical Research (Salt Lake City, UT)
- …procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. + Performs non-medical activities such as distribution ... of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. + Monitors subject safety. * Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. + Performs general housekeeping duties as… more
- Lilly (Boston, MA)
- …planning to close-out, ensuring adherence to timelines, budgets, and regulatory guidelines ( FDA , EMA, GCP, ICH) using a risk-based approach. + Develop and implement ... operational plans for clinical studies, managing CROs and vendors to ensure high-quality execution. + Lead internal clinical trial team meetings, tracking key study metrics (eg, enrollment, site feasibility, and data collection) to ensure progress and… more