What are the responsibilities and job description for the Regulatory Affairs Associate position at Next Code Placement?
Role Description
This is a full-time on-site role for a Regulatory Affairs Associate located in Bridgeport, CT. The Regulatory Affairs Associate will collaborate with teams to prepare, review, and manage regulatory documentation, ensure compliance with regulatory requirements, and support regulatory submissions. They will stay informed on industry regulations and guidelines while maintaining effective communication with regulatory authorities as needed.
Qualifications
- Proficiency in Regulatory Documentation and Regulatory Submissions
- Knowledge of Regulatory Compliance and Regulatory Requirements
- Experience or expertise in Regulatory Affairs
- Strong analytical and organizational skills
- Excellent written and verbal communication abilities
- Bachelor’s degree in Life Sciences, Regulatory Affairs, or a related field
- Prior experience in the pharmaceutical, biotechnology, or medical device industry is an advantage
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