- J&J Family of Companies (Irvine, CA)
- …may include; CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV). + Medical device experience highly preferred. + CRO experience and site management and ... Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and Market Access,… more
- Zimmer Biomet (Englewood, CO)
- …with respect to medical device development. + Understanding of medical device industry regulatory requirements required. + Proficient with CAD. ... Paragon 28, a Zimmer Biomet Company focusing on orthopedic medical devices for the foot and ankle....with 6+ years of experience + Prior experience in medical device development required. + Prior experience… more
- Bristol Myers Squibb (Seattle, WA)
- …years of industry experience in software development; experience in life sciences, medical devices , or regulated industries is highly desirable. + Proficiency ... laboratory information management systems (LIMS) or bioinformatics platforms. + Familiarity with regulatory standards for medical software (GMP, GxP, FDA, IEC… more
- Astrix Technology (Irvine, CA)
- …external requirements and standards, including FDA, ISO 13485, and other worldwide regulatory agencies pertaining to medical devices **Minimum ... Science + Years' Experience: 0-1 years + Familiarity with regulatory reporting requirements for medical devices... (eg MDRs, Vigilance reports, etc.) + Familiarity with medical device complaint files and quality records… more
- Rush University Medical Center (Chicago, IL)
- …practices as well as current rules and regulations of national and state regulatory agencies. * Understanding of basic medical physics and radiation dosimetry. ... **Job Description** Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Medical Physics… more
- Abbott (St. Paul, MN)
- …and market success. + **Technical & Regulatory Acumen** : Deep understanding of medical device standards and regulatory frameworks (eg, IEC 60601, IEC ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Insight Global (New York, NY)
- …affairs (especially product registration) -Experience within cosmetic, CPG, pharma, or medical device industries -Excel certification -Experience working with ... Job Description A large CPG client of ours is looking for a regulatory coordinator for a 5 month (starting) contract that will be focused on ensuring global product… more
- Veterans Affairs, Veterans Health Administration (Beckley, WV)
- …advanced MLT duties: i Knowledge of concepts, principles, methodology of medical laboratory technology, regulatory and accrediting agency requirements and ... Pathology and Laboratory Medicine Program at the Beckley VA Medical Center. The Medical Technician is responsible...judgment in adjusting either the procedure of the mechanical device to bring the procedures into good quality control.… more
- Bausch + Lomb (Clearwater, FL)
- …programming (eg, G-code) and controls (Haas, Fanuc, DAC, etc.). Understanding of regulatory requirements for medical device manufacturing. Proven leadership ... of vision correction implants. The Precision Machinist ensures compliance with stringent medical device industry standards and works closely with engineering,… more
- Trinity Health (Springfield, MA)
- …time **Shift:** Day Shift **Description:** Come join the Plant Operations team at Mercy Medical Center, part of Trinity Health Of New England! We are a member of ... rosters, etc. + Assists the Director with Joint Commission and other regulatory compliance, documentation, and other related regulatory duties. Supports all… more