research and/or clinical trial experience. Familiarity with MEDDEV 2.7/1 and EU MDR for clinical evaluations. Familiarity... and Global (US FDA, EU MDR) regulations. Experience working in a cross functional, collaborative environment and comfortable...
, with particular experience navigating EU MDR requirements for legacy and cleared devices. You design and oversee retrospective...
fibrosis and the first and only product approved in the EU as of September 2025. Reporting to the Senior Director, Global...
information under the California Privacy Rights Act (CPRA) and special category data under the UK and EU GDPR. Providing... does not “sell” or “share” personal information as defined by the CPRA. Outside of the United States, for example in the EU...
, FDA, and EU regulatory requirements. Excellent communication, documentation, and organizational skills. Ability...
as a subsidiary of Cipla (EU) Limited....
internationally or coordinating with EU-based teams Experience with CAD software or reviewing CAD drawings Familiarity with project...
cosmetic and personal care raw materials meet U.S. and international regulations, including FDA, EU Cosmetics Regulation, REACH..., nutraceutical, pharmaceutical, or food manufacturing. Knowledge of EU Cosmetics Regulation, REACH, and international compliance...
of U.S., EU, California, and Rest-of-World (ROW) regulatory and compliance requirements Demonstrated experience in Supplier...
category data under the UK and EU GDPR. Providing this information is optional and completely voluntary, and if you provide it... information as defined by the CPRA. Outside of the United States, for example in the EU, Switzerland and the UK, you may have the...