- North Coast Seafoods (Boston, MA)
- …work. + Safety & Compliance: Enforce safety regulations and compliance with OSHA, FDA , USDA, and GMP standards in a seafood manufacturing environment. + Inventory ... more
- Kedplasma (Cleveland, TN)
- …within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. Additionally, responsible for providing independent medical judgment and ... more
- Grifols Shared Services North America, Inc (San Diego, CA)
- …operations are conducted in full compliance with Grifols policies, regulatory (GMP, FDA , ISO) and safety requirements. + Directly participates in Bulking and Filling ... more
- Barilla (Ames, IA)
- …contact person for audit/inspection in the area of quality and food safety (eg FDA , FSSC 22000, Gluten Free, Organic, customers, etc). + Define budget and capex for ... more
- Philips (Malvern, PA)
- …of 7+ years' experience focused on Design Quality Engineering/Assurance within FDA regulated (ISO 13485) product environments, with proven experience implementing ... more
- Integra LifeSciences (Anasco, PR)
- …organization to ensure compliance with all appropriate regulations and standards, including FDA Part 820, ISO 13485, CMDR, MDR, MDSAP, and JPAL. Ensures compliance ... more
- University of Pennsylvania (Philadelphia, PA)
- …documents and materials (eg protocols, informed consent forms, institutional forms, FDA forms, continuing review and modification forms, deviation and exception ... more
- University of Pennsylvania (Philadelphia, PA)
- …residents, and medical students), grant applications, the development and submission of FDA IND applications, and the development of study specific forms and source ... more
- Philips (Bothell, WA)
- …a minimum of 7 years' experience in Regulatory Affairs within FDA regulated medical device/software (SaMD, SiMD) environments, AED's/Defibrillators or other Class ... more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …root cause analyses. + Strict adherence to procedures and practices according to FDA regulations. + Strong emphasis on documentation according to FDA ... more
- Compass Group, North America (West Chester, OH)
- …is responsible for development and maintenance of all QA programs, meeting USDA, FDA and customer requirements and ensuring the quality and safety of supplied goods. ... more
- University of Utah (Salt Lake City, UT)
- …made by sponsors or federal agencies. + Prepares, submits and maintains IRB , FDA , NIH and all other regulatory processes to ensure compliance with good clinical ... more
- University of Pennsylvania (Philadelphia, PA)
- …oversight submissions for regulatory documentation through the IRB, CTSRMC, FDA and all applicable institutional regulatory review committees. In collaboration ... more
- Lilly (Indianapolis, IN)
- …with, current local and international regulations, laws, guidance's (for example, FDA , ICH, CPMP etc.), Good Clinical Practices (GCPs), company standards, Lilly ... more
- Penn State Health (Hershey, PA)
- …X-ray Absorptiometry The Nuclear Medicine Division performs all types of FDA -approved oncologic PET/CT, Amyloid and metabolic brain PET/CT, cardiac Rb-82 PET/CT, ... more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …Become a **maker of possible** with us. **Responsibilities** + Maintain FDA (Food & Drug Administration) and ISO (International Organization for Standardization) ... more
- Abbott (Plymouth, MN)
- …personnel. + Reviews device labeling and marketing materials for compliance with FDA submissions and applicable regulations. + Interfaces directly with FDA ... more
- System One (Houston, TX)
- …supporting the company's clinical operations function in the management of the FDA required pediatric trial in chronic sinusitis. This includes working directly with ... 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
- Catalent Pharma Solutions (Harmans, MD)
- **Manufacturing Technical Operations Specialist III** **Summary:** _Our FDA -licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on ... more