Regulatory Affairs Specialist – Insight Global

Company: Insight Global

Location: New York City Metropolitan Area

Salary: Not specified

Employment Type: Contract

Seniority Level: Mid-Senior level

Applicants: 78

Apply on LinkedIn

Job Description

12-month contract to start **********

JOB DESCRIPTION

Insight Global is seeking a Regulatory Affairs Specialist (Technical Support, Global Cosmetics) for a top prestige hair care client. This individual will play a hands-on role supporting global regulatory activities across a cosmetics portfolio, ensuring compliant product development and commercialization. The ideal candidate has strong experience in cosmetic ingredient compliance, documentation management, and formulation review, and thrives in a collaborative, fast-paced environment while partnering closely with R&D, suppliers, and internal stakeholders to enable efficient and compliant product launches.

Responsibilities

• Conduct raw material and ingredient compliance reviews for global cosmetic regulations

• Obtain, review, and maintain supplier regulatory documentation

• Support formula-level regulatory assessments and flag non-compliant ingredients

• Collaborate with R&D on formulation reviews and compliant alternatives

• Generate and review INCI ingredient lists for labeling and artwork

• Support label compliance across global, federal, and state requirements

• Prepare regulatory and technical documentation for retailers and partners

• Assist with product registrations and market-specific documentation

• Monitor U.S. and global regulatory updates impacting formulations

• Maintain organized regulatory records, trackers, and compliance documentation

• Act as a liaison between Regulatory, R&D, Supply Chain, and suppliers

REQUIRED SKILLS AND EXPERIENCE

• Bachelor’s degree in Chemistry, Biology, Regulatory Affairs, or related scientific field

• 2–5 years of regulatory affairs or technical regulatory support experience in cosmetics/personal care

• Strong knowledge of cosmetic ingredient regulations and INCI nomenclature

• Hands-on experience reviewing raw material documentation (SDS, COAs, specs, regulatory declarations)

• Experience supporting formulation compliance and ingredient reviews

• Strong attention to detail and documentation accuracy

• Ability to manage multiple priorities in a fast-paced environment

NICE TO HAVE SKILLS AND EXPERIENCE

• Experience with U.S. FDA cosmetic regulations and state laws (e.g., California)

• Familiarity with international/global cosmetic regulatory requirements

• Experience supporting labeling, artwork review, and retailer documentation

• Experience working cross-functionally with R&D, Supply Chain, and external suppliers

• Background in environmental or emerging regulatory compliance

Disclaimer: This job listing is sourced from LinkedIn and is provided for informational purposes. Apply directly through the employer’s application process. Medical Device Navigator is not affiliated with the hiring company.
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