What are the responsibilities and job description for the Labeling Process Improvement Consultant position at i-Pharm GxP?
Job Summary
i-Pharm GxP is seeking an experienced Regulatory Labeling Consultant to join our team. In this role, you will be responsible for maintaining and updating our regulatory labeling systems, collaborating with cross-functional teams, and managing label change requests.
Responsibilities:
- Develop and implement process improvements to enhance efficiency and compliance.
- Manage labeling projects from initiation to execution.
- Provide technical expertise and support for labeling issues.
Requirements:
- Bachelor's degree in Regulatory Affairs, Engineering, or a related field.
- 3-5 years of experience in regulatory labeling within the pharmaceutical or medical device industry.
- Strong knowledge of cGMP, FDA, EMA, and USP guidelines.
- Experience with label artwork changes, regulatory submissions, and quality systems.
The ideal candidate will have excellent communication and project management skills, as well as the ability to work collaboratively in a team environment.
