- Medtronic (Lafayette, CO)
- …medical device industry standards and regulatory requirements to include Food and Drug Administration ( FDA ) regulations, ISO 13485, ISO 14971, 21 CFR ... devices. Must possess at least four (4) years' experience with each of the following: FDA regulations, 21 CFR Part 820, ISO 13485, ISO 14971, IEC 60601, CAPA, and… more
- Abbott (Houston, TX)
- …and professional work environment. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... and monitor effectiveness of engineering systems and procedures to ensure compliance to FDA , GMP, and all other applicable agency regulations. + Ensure a safe work… more
- Saint Francis Health System (Tulsa, OK)
- …boards (IRB), National Institutes of Health (NIH), and the Food and Drug Administration ( FDA ) requirements. Analyzes documentation and reporting of any ... research experience, preferred. Knowledge, Skills, and Abilities: Proven knowledge of FDA , IRB, and NIH regulatory requirements. Proficient knowledge of Microsoft… more
- Abbott (Portland, OR)
- …as a Core Team Member) + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating ... experience and demonstrated use of Quality tools/methodologies + Detailed knowledge of FDA , GMP, ISO 13485, and ISO 14971 + Project management and leadership… more
- Charles River Laboratories (Spencerville, OH)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on… more
- Charles River Laboratories (Spencerville, OH)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...We are seeking an Administrative Assistant, Reception for our Administration team at our Safety Assessment site located in… more
- Charles River Laboratories (Spencerville, OH)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...are seeking a Temporary Part-Time Company Driver for our Administration team at our Safety Assessment site located in… more
- Charles River Laboratories (Spencerville, OH)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...preparation of test materials and dietary admixtures for dose administration , as well as maintaining the general cleanliness of… more
- Bristol Myers Squibb (Princeton, NJ)
- …device, biologics) facilities and have worked for the US Food & Drug Administration ( FDA ), within the past 10 years (2015-2025) in a Consumer Safety ... Officer (CSO) or similar role; minimum of 5 years' experience as a CSO required. * Demonstrated negotiation, risk management, relationship management and conflict resolution skills. * Proven ability to understand complex processes/problems and propose… more
- Bristol Myers Squibb (Trenton, NJ)
- …(medical device, biologics) facilities and have preferably worked for the US Food & Drug Administration ( FDA ), within the past 5 years (2015-2025) in a ... Consumer Safety Officer (CSO) or similar role; minimum of 2 years' experience as a CSO preferred. * Proven ability to understand complex processes/problems and propose alternate solutions. * Demonstrates innovation, flexibility, open-mindedness, and… more