- Adecco US, Inc. (Cupertino, CA)
- …is experienced in medical device labelling and a solid understanding of domestic and international regulatory requirements, including 21 CFR 801 and EU MDR. This ... evolving global standards and regulatory requirements + Collaborate with Regulatory Affairs to incorporate country-specific labelling and translations +… more
- Abbott (Sylmar, CA)
- …medical device products. Coordinates with Engineering, Marketing, Clinical Research, and Regulatory Affairs to define product labeling requirements. Designs and ... and IFUs from Engineering (Manufacturing, Packaging, etc.), Marketing, Clinical Research, and Regulatory Affairs (RA) to define specific requirements for product… more
- Actalent (Irvine, CA)
- …working cross-functionally with departments such as Advanced Operations, Product Development, Regulatory Affairs , and Marketing. + Strong interpersonal, written, ... Job Title: Document Control Specialist For immediate consideration, please apply directly to..., responsible for ensuring compliance with internal and external regulatory requirements, including FDA, ISO, and MDD standards. You… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …+ At least one year of relevant experience in pharmacovigilance, clinical research, or regulatory affairs in a CRO or a pharmaceutical company is usually ... Would you like to join an international team working to improve the future of...deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data review, compilation and… more
- Edwards Lifesciences (Irvine, CA)
- …at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based ... development and HCP engagement to field teams, marketing teams and international Professional Education teams leveraging best practices + Provide direction and… more