Sr. Regulatory Affairs Associate- CONSULTANT

We are searching for a Sr. Regulatory Affairs Associate Consultant to work with a client on a 12-month contract. The role involves collaborating with the client's regulatory project team, identifying regulatory requirements, and reviewing documents.

Requirements

• Bachelor's degree in life sciences (preferred)
• Minimum of 1 year of working experience in Medical Device Regulatory Affairs/training in Regulatory Affairs focused on EU MDR
• Knowledge of FDA Medical Device regulations, ISO13485, EU MDD/MDR
• Proficient in Microsoft Office (e.g., Word, Excel, PowerPoint)
• Strong proficiency in written and verbal English communication

Benefits

• Contract role with possibility of extension
• Opportunity to work with a global CRO
• Client-facing role with a high-trust environment