Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU)

Coronado Research
Portsmouth
1 week ago
Create job alert

Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU)

Join to apply for the Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU) role at Coronado Research

Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU)

3 days ago Be among the first 25 applicants

Join to apply for the Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU) role at Coronado Research

Get AI-powered advice on this job and more exclusive features.

Freelance Director of Regulatory Affairs - Cosmetics (U.S. & EU)

Location: Remote

Contract Type: Freelance / Consultant

Reports To: EVP Regulatory Affairs

Position Overview:

We are seeking an experienced and strategic Regulatory Affairs Director with expertise in cosmetic product regulations across the United States and European Union. This freelance role is ideal for a professional who can lead compliance efforts, manage regulatory submissions, and guide product development in line with evolving global legislation.

Key Responsibilities:

Regulatory Strategy & Compliance

- Develop and implement regulatory strategies aligned with:

- U.S. regulations under the Federal Food, Drug, and Cosmetic Act (FD&C Act) and the Modernization of Cosmetics Regulation Act (MoCRA).

- EU regulations, including Regulation (EC) No 1223/2009 and its amendments such as Regulation (EU) 2025/877.

- Ensure product safety, labeling, and marketing materials comply with:

- FDA requirements for facility registration, product listing, adverse event reporting, and safety substantiation.

- EU mandates on ingredient bans, nanomaterial restrictions, and CMR substance prohibitions.

Product Development Support

- Advise on regulatory implications of formulations and claims.

- Review technical documentation, ingredient safety data, and labeling for compliance.

Submission & Communication

- Manage:

- FDA Voluntary Cosmetic Registration Program (VCRP) and Cosmetic Product Ingredient Statements (CPIS).

- Liaise with FDA, EFSA, European Commission, and national competent authorities.

- Conduct regulatory risk assessments and develop mitigation strategies.

- Maintain comprehensive regulatory documentation and ensure audit readiness.

Qualifications:

- 10+ years' experience in regulatory affairs, with a focus on cosmetic products.

- Proven success navigating FDA, MoCRA, and EU Regulation 1223/2009 compliance.

- Strong understanding of:

- Good Manufacturing Practices (GMP) and labeling laws in both regions.

- EU Annex II (prohibited substances), Annex III (restricted substances), and Annex V (preservatives).

- Excellent communication, analytical, and project management skills.

- Ability to work independently and manage multiple international projects.

Preferred Skills:

- Advanced degree in Science, or related field.

- Experience with digital regulatory platforms and dossier preparation tools.

- Familiarity with nanomaterial, fragrance allergen, and CMR substance regulations.

- Flexible hours and remote work.

- Opportunity to shape regulatory strategy for innovative beauty and personal care products.

Seniority level

  • Seniority levelDirector

Employment type

  • Employment typePart-time

Job function

  • Job functionConsulting

Referrals increase your chances of interviewing at Coronado Research by 2x

Get notified about new Director of Regulatory Affairs jobs in Greater Portsmouth Area.

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.


#J-18808-Ljbffr

Related Jobs

View all jobs

Regulatory Affairs Biologics Consultant, Veterinary

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.

Why Medical Technology Careers in the UK Are Becoming More Multidisciplinary

Medical technology (medtech) is transforming healthcare in the UK — from wearable sensors to AI diagnostic tools, from surgical robots to telemedicine platforms. Advances in hardware, software, data and connectivity are enabling more personalized, efficient and accessible care. But with great power comes great responsibility. As medical devices and health technologies enter hospitals, clinics and consumers’ homes, professionals in this domain must master much more than engineering and algorithms. They must also understand law, ethics, psychology, linguistics & design. That is, medtech careers are now deeply multidisciplinary. In this article, we explore why medical technology careers in the UK are becoming more multidisciplinary, how these five allied fields now intersect with medtech work, and what job-seekers and employers should do to succeed in this evolving ecosystem.

Medical Technology Team Structures Explained: Who Does What in a Modern MedTech Department

Medical technology (MedTech) spans everything from wearable health devices and surgical robots to diagnostic imaging, in-vitro diagnostics (IVD), digital therapeutics, AI-driven triage, and Class I–III medical devices. In the UK, the sector touches NHS care pathways, private providers, and global markets—with stringent expectations for safety, clinical evidence, cybersecurity, and data privacy. As ventures scale from prototype to regulated product, clear team structures become the difference between promising pilots and licensed, market-ready devices. Whether you’re hiring your first clinical specialist or applying for a role in QA/RA, this guide explains who does what in a modern MedTech department, how functions collaborate across the product lifecycle, UK-typical skill sets and salaries, common pitfalls, and best practices for building a resilient team.