- University of Utah (Salt Lake City, UT)
- …international research consortia. 7. Assists with the preparation and submission of IRB , FDA , NCI , NIH , NSF and/or other regulatory documents and research ... more
- Kelly Services (Sunnyvale, CA)
- …development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle ... more
- AbbVie (North Chicago, IL)
- …impact to ABBV overall. + Manages interface with Health Authority ( FDA ) for key projects/issues, including direct collaboration with review division personnel. ... more
- Interstate Blood Bank (Vista, CA)
- …in the GBS DDL. * Assist Regulatory Management with product deviation reporting to the FDA . * Updates and distributes annual facility FDA reports. * Assists with ... more
- Imperative Care (Campbell, CA)
- …team and ensure compliance with domestic and international regulatory standards (eg, FDA , CE marking, etc.). + Build and sustain relationships with cross-functional ... more
- Owens & Minor (Indianapolis, IN)
- …information, cylinder maintenance and inspection logs and materials required by the FDA * Oversee the shipping, receiving and distribution of USP Medical Oxygen ... more
- General Dynamics Information Technology (Fort Detrick, MD)
- …information amendments, clinical protocols and study reports, investigator's/investigational brochures, FDA meeting requests and background materials, responses to ... more
- Danaher Corporation (Austin, TX)
- …GCP auditing (ie, TMF, SOP compliance, training, etc.), interface to the FDA and notified bodies, clinical CAPA management, and IVDR compliance across Clinical ... more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …plasma derived pharmaceuticals. + Strict adherence to procedures and practices according to FDA regulations. + Strong emphasis on documentation according to FDA ... more
- University of Utah (Salt Lake City, UT)
- …of and at the close of the study. 11. Prepares, submits and maintains IRB , FDA , NCI , NIH , NSF and/or other regulatory documents and research correspondence. 12. ... more
- BD (Becton, Dickinson and Company) (Covington, GA)
- …in compliance with applicable Quality Systems regulations, ISO standards, FDA regulations, and Corporate, Division, and International policies and procedures. ... more
- Veterans Affairs, Veterans Health Administration (Houston, TX)
- …compliance with all QC and QA requirements as per VHA policy, FDA /MQSA regulations, and ACR standards in mammography, tomography, breast ultrasound, and image ... more
- Compass Group, North America (Greenville, SC)
- …Director is responsible for developing and maintaining all QA programs, meeting FDA , customer, and Corporate requirements, ensuring the quality and safety of ... more
- Corning Incorporated (Durham, NC)
- …for ensuring the plant complies with ISO 13485, MDD 93/42/EEC and FDA requirements; facilitates audit programs for all facets of the manufacturing process, ... more
- Catalent Pharma Solutions (Harmans, MD)
- …of life-enhancing and life-saving treatments for patients annually. Our FDA -licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located ... more
- Actalent (Chanhassen, MN)
- …+ Assist in the implementation of corrective actions resulting from the FDA audit conducted in December. + Conduct routine and non-routine analysis of ... more
- Abbott (Columbus, OH)
- …implementation of the CAPA management system + Develop, execute and review FDA validation protocols and related documentation in accordance with procedures and ... more
- Actalent (Oak Creek, WI)
- …and company policies. This role ensures compliance with GMP, SQF, HACCP, FDA , and State regulations through auditing, verification of Certificates of Analysis ... more
- Sysco (Lancaster, CA)
- …food safety regulatory requirements (Federal, State/Provincial and, Local) including US FDA Seafood HACCP, FSMA Preventive Controls for Human Foods, FSVP, 204 ... more
- Owens & Minor (Suwanee, GA)
- …information, cylinder maintenance and inspection logs and materials required by the FDA + Oversee the shipping, receiving and distribution of USP Medical Oxygen ... more