This is a full-time, on-site role for a Regulatory Affairs Associate. The Regulatory Affairs Associate will be responsible for managing regulatory documentation, ensuring compliance with regulatory requirements, and handling regulatory submissions. They will also provide support for regulatory affairs tasks and projects.
Qualifications:
- Strong knowledge of regulatory documentation, compliance, requirements, and submissions
- Experience in managing regulatory affairs tasks
- Attention to detail and ability to work with complex regulatory information
- Excellent organizational and time management skills
- Strong written and verbal communication skills
- Ability to work effectively in a team and independently
- 5+ years of experience in the pharmaceutical or medical device industry
- Bachelor’s degree in a relevant field
Skills:
- Regulatory Affairs
- Regulatory Submissions
- Compliance Management
- Documentation
- Project Support
- Communication