- DEKA Research & Development (Manchester, NH)
- …Documentation Practices; meets QMS requirements; and complies with US Food and Drug Administration ( FDA ) regulations / other regulatory requirements. + ... investigations, medical device reporting, or product analysis. + Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device… more
- DEKA Research & Development (Manchester, NH)
- …Documentation Practices; meets QMS requirements; and complies with US Food and Drug Administration ( FDA ) regulations / other regulatory requirements. + ... industry or in a clinical setting is preferred. + Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting… more
- Abbott (Houston, TX)
- …and other regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... experience and demonstrated use of Quality tools/methodologies. + Detailed knowledge of FDA , GMP, ISO 13485, and ISO 14971 + Solid communication and interpersonal… more
- Terumo Medical Corporation (Elkton, MD)
- …with internal and external shops. 12. Comply with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... processes or equivalent education and experience + Experience in an FDA regulated industry, medical device or pharmaceutical preferred + Experience with… more
- Abbott (Plymouth, MN)
- …complaints in alignment with Abbott goals. + Follows US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... skills, as well as attention to detail. **Preferred** **Qualifications** + Detailed knowledge of FDA , GMP, and ISO 13485 + ASQ CQT, CQE, CQA certification + Six… more
- Cedars-Sinai (Los Angeles, CA)
- …Ensures compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. + Maintains ... study budget and patient research billing. Ensures compliance with all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study and… more
- Abbott (Liberty, SC)
- …and other regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... and process development from concept through sustained manufacturing of FDA regulated products. Responsible for production support, maintenance support, performing… more
- Abbott (St. Paul, MN)
- …and other regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) and international regulations, other regulatory requirements, ... new and modified products. + Prepares robust regulatory applications for FDA and/or international regulatory agencies to achieve departmental and organizational… more
- Abbott (Atlanta, GA)
- …and other regulatory requirements. * Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... experience and demonstrated use of Quality tools/methodologies. + Detailed knowledge of FDA , GMP, ISO 13485, and ISO 14971 Solid communication and interpersonal… more
- Abbott (Sylmar, CA)
- …and other regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... and issue-tracking tools such as GIT, Jira, Subversion, ClearQuest, Doors, Bugzilla. + Knowledge of FDA 21 CFR part 820, 21 CFR part 11, GMP, IEEE 1012, IEC 62304… more