Description
**Job Description**
2\.1 FDA Data Collection and Management
Contact suppliers to verify that all received data is complete and accurate.
Photos of components required for the production process, including updates provided by suppliers.
2\.2 Data Analysis
Review and analyze the list of documents retained by CBP, identifying potential risks or required actions.
2\.3 Continuous Improvement
Monitor changes in regulatory frameworks and implement updates to data practices.
3\.1 Experience / Technical Knowledge
English 60 \- 75 % written and spoken
3\.2 Competencies / Soft Skills
Basic knowledge of regulatory terminology is a plus.
Detail-oriented and organized
Strong work ethic and eagerness to learn
Problem-solving mindset
3\.3 Academic Qualifications
Bachelor's degree / shortened program
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.