- Vanderbilt University Medical Center (Franklin, TN)
- **Discover Vanderbilt University Medical Center** : Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, ... all messages using correct spelling, grammar, and commentary appropriate for medical record documentation. + Demonstrate ability to identify and proactively assist… more
- AbbVie (North Chicago, IL)
- …experience within one of the most dynamic organizations in the pharmaceutical and medical device industry. You will support the Internal Audit & Inspection ... research, business administration in a healthcare setting or auditing, regulatory affairs , or other related degree +...between December 2026 - June 2027 Preferred Qualifications + Medical device or project management experience Additional… more
- J&J Family of Companies (Titusville, NJ)
- …and Device Development and Regulation, Program Management, Regulatory Affairs Management, Relationship Building, Safety-Oriented, Scientific Research, ... via matrix interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, quality… more
- Mallinckrodt Pharmaceuticals (St. Louis, MO)
- …in the area of Quality Systems for pharmaceutical products and medical devices . + Experience interacting with regulatory agencies such as the FDA and ... of 15 years of pharmacuetical industry experience in a Quality Assurance and/or Regulatory Affairs function including experience in manufacturing and control of… more
- HRPivot (Tucson, AZ)
- …proven R&D leader to drive the development of a highly advanced Class III medical devices through concept, preclinical, and clinical stages to FDA PMA approval. ... the design, development, and advancement of innovative Class III medical devices through all stages of the...studies, preclinical testing, and clinical studies. + Partner with Regulatory Affairs and Clinical teams to support… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …integration testing + Familiarity with regulatory requirements for software in medical devices (eg, FDA QSR, ISO 13485) + Excellent leadership, ... teams, including software development, product management, quality assurance, and regulatory affairs , to ensure alignment and a...team + Proven experience in a regulated industry, preferably medical device , in-vitro diagnostics (IVD), or a… more
- Abbott (Abbott Park, IL)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... Experience** + Associate's degree required + 7 years of Cath Lab and/or Medical Device experience **Preferred Experience** + Bachelor's Degree highly preferred.… more
- Bausch + Lomb (Clearwater, FL)
- …industry best practices. This includes the development, manufacturing and release of medical device product. KEY ACTIVITIES / RESPONSIBILITIES **Micro lab ... equipment, or process changes before implementation + Collaborate with Quality and Regulatory Affairs to resolve any discrepancies or nonconformances before… more
- City of Jacksonville (Jacksonville, FL)
- …and laptop computer, motor vehicle, hand tools, and standard measuring devices . The physical demands consist of driving, sitting, climbing, standing, walking, ... and plans. + Issues building code citations and presents cases before regulatory agencies. + Investigates reported code violations and secures evidence in cases… more
- City of Jacksonville (Jacksonville, FL)
- …and laptop computer, motor vehicle, hand tools, and standard measuring devices . The physical demands consist of driving, sitting, climbing, standing, walking, ... and plans. + Issues building code citations and presents cases before regulatory agencies. + Investigates reported code violations and secures evidence in cases… more