Regulatory Affair Associate - Cosmetic & Skincare
Englewood Lab, Inc
Totowa, new jersey
Job Details
Full-time
Full Job Description
Responsibilities:
- Responsible for generating ingredient lists, quantitative formulas, exploded formulations (Decks), as well as multiple document types.
- Generate raw material regulatory statement: origin, cruelty-free, BSE & TSE, heavy metal, impurity, REACH-Compliance, global & regional compliance, food allergen, fragrance allergen, nitrosamine-free, vegan, gluten-free, nano, CMR, etc.
- Generate Finished Good SDS.
- Generate a global compliance report and review the report against jurisdictional compliance.
- Review formulas either using the software system or the PCPC International Raw Material Database.
- Responsible for gathering portions or all of the PIFs (Product Information Files) for the EU registration.
- Communicate with Vendors/suppliers for RM documents and follow up on requests with vendors.
- Communicate with customer service personnel and EWL chemist to give project status information and communicate any discrepancies.
- Responsible for any additional duties or assignments as directed by the Manager of Regulatory Affairs.
Requirements
- BS Degree in Chemistry or related science field
- Strong organization skill is a must
- Strong computer skills
- Ability to review and understand complicated regulatory rulings
- A strong work ethic and ability to change directions when needed
Benefits
- Medical, Dental, and Vision Insurance
- Life Insurance 100% contributed by the Company
- 401k after 6 months