- Hologic (Louisville, CO)
- Regulatory Affairs Specialist , Medical Device Louisville, CO, United States Marlborough, MA, United States **Join Hologic's Surgical Division as a ... Regulatory Affairs Specialist ** Are you...industry. **What You'll Bring:** **Experience** + 2-5 years in regulatory affairs , preferably within the medical… more
- Medtronic (Lafayette, CO)
- …in a more connected, compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist is responsible for planning and executing global ... assigned product family. This role partners with the international regulatory affairs group to support global submissions...understanding of FDA and MDR requirements. + Knowledge of Medical Device Quality Systems (21 CFR 820, ISO 13483)… more
- BD (Becton, Dickinson and Company) (Louisville, CO)
- **Job Description Summary** The Regulatory Affairs Specialist II is responsible for implementation of strategies including domestic and international ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...with software and capital systems is a plus. + Regulatory Affairs Certification (RAC) desired At… more
- Bausch + Lomb (Denver, CO)
- …with ongoing regulatory training related to products. + Works closely with the Regulatory Affairs labeling group in order to assess and determine the impact ... preferred or equivalent + Minimum of 6 years in Regulatory Affairs or relevant experience in a...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
- Bausch + Lomb (Denver, CO)
- …Bachelor degree or equivalent, Master degree preferred + Minimum of 8 years in Regulatory Affairs or relevant experience in a regulated environment + Ability to ... and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
- Bausch + Lomb (Denver, CO)
- …degree or equivalent; Master's degree preferred + Minimum of 8 years in Regulatory Affairs with experience in the consumer product (Rx/OTC, OTC Monograph, ... and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
- Nestle (Denver, CO)
- …the future of health and nutrition for patients and consumers. **Position Summary:** The Regulatory Operations Specialist will be a key contributor to the Pharma ... dossier events and requirements to drive the execution of submissions. The Regulatory Operations Specialist must have Regulatory Operations/Publishing… more
- Cardinal Health (Denver, CO)
- …and regulatory submissions. **_Job Summary_** The Senior Regulatory Specialist , Data Management & Governance for Medical Devices plays a critical ... **_What Regulatory Affairs contributes to Cardinal Health_**... and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory … more
- Aegon Asset Management (Denver, CO)
- …General Counsel, Risk, Internal Audit, Strategy and Development, and Corporate Affairs , which covers Communications, Brand, and Government and Policy Affairs ... For more information, visit transamerica.com . Job Description Summary The Specialist Enterprise Architect will lead WFG's digital transformation by designing… more
- Medtronic (Denver, CO)
- …groups (Monitoring, Data Management, Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs , Legal, and European Clinical groups). + ... to one-half of adults. We are seeking a **Sr. Field Clinical Research Specialist ** who will have the responsibility of providing technical and educational support to… more
- Edwards Lifesciences (Denver, CO)
- …patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you ... Knowledge and understanding of cardiovascular science + Moderate understanding of medical device regulatory requirements and documents, device accountability and… more