- BD (Becton, Dickinson and Company) (San Diego, CA)
- …robust field action solutions. + Familiarity with CAPA, risk management, and FDA documentation. + Strong writing and organizational skills. + Detail-oriented and ... comfortable working in a fast-paced environment. + Knowledge of ISO 14971, ISO 13485, ISO 9001, 21 CFR Part 820 At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential… more
- Veterans Affairs, Veterans Health Administration (Madison, WI)
- …Association (NFPA), Nuclear Radiation Commission (NRC), Food and Drug Administration ( FDA ), the Joint Commission (TJC), and the American College of Radiology ... (ACR). Ability to resolve complex failures on imaging equipment and clinical systems. Ability to perform advanced testing to troubleshoot imaging equipment and clinical system interfaces. Reference: For more information on this qualification standard, please… more
- United Therapeutics (Silver Spring, MD)
- …pulmonary arterial hypertension ( **PAH** ). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung ... disease ( **PH-ILD** ) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis ( **PF** ). The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is… more
- US Tech Solutions (Marlborough, MA)
- …including Occupational Safety and Health Administration (OSHA), Quality System Regulations ( FDA ), ISO 13485, MDD, PAL, CMDCAS, KFDA, other country specific ... Regulations as applicable. 7. May perform other related duties as assigned by Supervisor. Quality Systems Duties and Responsibilities: Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Qualifications 3 - 5… more
- PCI Pharma Services (Philadelphia, PA)
- …and installation to meet customer requirements. + Assure compliance to GMP's, SOP's, FDA , DEA and OSHA rules and regulations. + Interact with all customers and ... management to achieve objectives. + Able to balance multiple issues simultaneously in a fast pace environment + Coordinate resources with requirements that are driven by the production schedule. + Instruct mechanics on their job assignments and their… more
- Kelly Services (Clearwater, FL)
- …product meets all acceptable criteria per SOPs + Following all FDA /CGMP regulations regarding traceability and safety procedures + Supporting, encouraging, and ... participating in team-related activities + Assisting in training manufacturing associates + Reporting unusual conditions and problems to supervisor and manufacturing lead + Practicing good housekeeping **This job might be an outstanding fit if you:** + Have a… more
- Charles River Laboratories (Raleigh, NC)
- …proudly supported the development of 86% of the drugs approved by the FDA in 2021. **Equal Employment Opportunity** Charles River Laboratories is an Equal ... Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. If you are interested in applying to… more
- ManpowerGroup (Newark, DE)
- …focus on analytical testing and instrumentation. + Knowledge of quality management systems, FDA , QSR, ISO, and IVDD standards. + Proficiency with MS Office, SAP, ... LIMS, and Siemens Clinical testing software. + Strong laboratory skills, including operation, maintenance, and troubleshooting of analytical instruments. + Excellent communication skills and the ability to work independently or as part of a team. **What's in… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to ... reduce infarct size in patients with the most severe heart attacks. Heart disease is the leading cause of death for both men and women in the US At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need.ZOLL has been… more
- ICON Clinical Research (PA)
- …according to the sponsor's protocol and in compliance with all applicable FDA regulations/ICH GCP guidelines and local regulations, ensuring the welfare and safety ... of human subjects. This position is office based in John's Creek, GA. Work hours: **Monday-Friday, 11:00 AM-7:00 PM** . Ideally, the schedule would also include **one Saturday per month** , with a weekday provided off in lieu. **What You Will Be Doing:** +… more