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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


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