REGULATORY AFFAIRS ASSOCIATE
READING, PA 19602
The Ideal Candidate should have 1-3 years experience in regulatory documentation such as but not limited to-Issue Ingredient lists, maintain and prepare SDSs, domestic/foreign compliance for personal care products, source and maintain ingredient documentation in an R&D administrative support role.
-Manage raw materials in database inclusive of regulatory restrictions
-Communicate with raw material suppliers for information.
-Data entry to FDA and other related registration websites and internal systems.
-Attend seminars and keep current with changing guidelines.
-Communicate effectively with R&D lab as well as other departments
-Review raw materials and Formula for compliance with current global regulations and customer restrictions
-Manage formula approvals, including issuance of ILs or other regulatory documents for customer review
- Excellent verbal and written communication skills, proficient in Outlook, Excel, Word
- Work independently and in a group, detail-oriented with good organization skills.
If qualified, please send resumes to Andy email@example.com or call 610.981.4816