Intern - Regulatory

Dermalogica • Carson, CA

11h

About The Position

Dermalogica stands tall as a beacon in the professional skincare realm, winning the trust of skin therapists across the globe. As a shining gem in the crown of the Unilever Prestige family, our commitment isn't just to nurture skin, but also to redefine industry standards with revolutionary skincare innovations. With a commitment to innovation, sustainability, and excellence, Dermalogica has been at the forefront of the skincare industry for over three decades. Bolstered by our International Dermal Institute the apex of post-graduate skin and body therapy training we are on an exhilarating journey of expansion. And you could be a part of this adventure! We are currently seeking a curious, meticulous Regulatory Intern to join our Research & Development team during an exciting period of growth and innovation. This internship offers firsthand exposure to cosmetic and OTC regulatory processes while supporting new product launches and our existing product portfolio. This is an excellent opportunity for a science-focused student who is eager to learn, contribute, and gain real-world experience within a fast-paced, collaborative R&D environment.

Requirements

• Familiarity with or interest in a laboratory environment
• Strong interest in cosmetic and/or OTC regulations
• Ability to manage multiple tasks, prioritize effectively, and meet deadlines.
• Strong attention to detail with the ability to multitask efficiently.
• Excellent organizational, written, and verbal communication skills
• Proficiency in Microsoft Word and Excel
• Currently enrolled in and pursuing a bachelors degree, preferably in a science-related field
• 01 years of experience; prior exposure to cosmetic, pharmaceutical, food, or science-based environments is a plus, but not required

Responsibilities

• Partnering with external suppliers to collect and organize raw material data, escalating requests when needed.
• Maintaining and updating the raw material database to ensure accuracy and compliance
• Supporting R&D with sample initiation, scheduling, preparation, packing, and coordination of product testing and clinical trials
• Assisting with regulatory documentation related to product development, validation, and registration
• Supporting the International Regulatory documentation process within the Product Information Management (PIM) system
• Tracking and logging international requests to ensure proper communication and queries are addressed in a timely manner
• Manage safety testing spreadsheet logs
• Maintaining validation documentation within R&D and International folders
• Coordinate with chemists to support in samples submission for testing

What This Job Offers

• Career Level: Intern