Cosmetics Regulatory Affairs Specialist

Thg Plc; Edison (NJ); Sur place; USD 70 000 - 81 000; Plein temps

Résumé du poste

Bentley Laboratories, a premier beauty contract manufacturer based in Edison, NJ, is seeking a Regulatory Affairs Specialist to join the THG Beauty Manufacturing division. You will coordinate regulatory documentation, review ingredients, support labeling, and help ensure products meet regulatory requirements across markets.

Reporting to the Regulatory Affairs Manager, you will organize data in ERP systems, interact with R&D, QA, and suppliers, and assist with testing programs and customer

Qualifications

• Approximately 3 years of experience in Regulatory Affairs or related function in cosmetics/OTC or regulated industry.
• Working knowledge of FDA requirements, labeling, ingredient documentation, and regulatory compliance.
• Experience preparing regulatory documentation, coordinating testing activities, and supporting technical or customer requests.
• Strong organization, attention to detail, communication, and project management skills.
• Proficiency in Microsoft Office and ability to learn regulatory databases and ERP systems.

Responsabilités

• Regulatory Documentation & Product Records: maintain documentation, data, supplier docs, and customer packages.
• Formula, Claims & Labeling Support: review formulas, support declarations and attestations, ensure labels are compliant.
• Product Testing & Laboratory Coordination: coordinate third‑party testing, track stability and testing programs.
• Compliance & Cross‑Functional Collaboration: respond to inquiries, collaborate with R&D, Quality, Operations, suppliers and labs; assist audits.

Connaissances

Regulatory affairs

FDA requirements

Documentation

Organization

Microsoft Office

ERP systems

Formation

Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related

Description du poste

Bentley Laboratories, a premier beauty contract manufacturer based in Edison, NJ, is seeking a Regulatory Affairs Specialist to join the THG Beauty Manufacturing division. You will coordinate regulatory documentation, review ingredients, support labeling, and help ensure products meet regulatory requirements across markets.

Reporting to the Regulatory Affairs Manager, you will organize data in ERP systems, interact with R&D, QA, and suppliers, and assist with testing programs and customer