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Careers at Cosmereg

Regulatory Affairs Careers in Cosmetics & Consumer Health

Since 2013US · EU · UK · Canada · UAEOffice & hybrid roles

Cosmereg is a regulatory affairs consultancy founded in 2013, supporting cosmetic, OTC, food, supplement and medical device companies in the US, EU, UK, Canada and UAE. Our consultants combine scientific training with hands-on regulatory experience, and we continually look for qualified professionals to join the team.

Submit your CV Profiles we look for
Why Cosmereg

Why work with us

A specialist consultancy where scientific rigour, confidentiality and client trust come first.

Multi-market exposure

Work across FDA/MoCRA, EU 1223/2009, UK, Health Canada and UAE frameworks, often for the same client and product range.

Hybrid working model

Depending on the role, our team works from our offices in the United States, United Kingdom, Ireland and the UAE, combined with structured remote collaboration across time zones.

Continuous learning

Regulations change constantly. Our team receives ongoing training on regulatory updates and works under the guidance of senior consultants.

A multilingual team

We work with clients in English, Spanish, Italian, French, Korean and more. Extra languages are a real asset here.

Rigorous quality standards

Every regulatory deliverable follows documented procedures and goes through a four-eyes review before it reaches the client.

Structured career development

A clear path from associate to consultant and senior consultant, with responsibility for clients, markets and specialist areas as experience grows.

Talent we recruit

Profiles we are always looking for

There are no advertised vacancies at the moment. These are the profiles we recruit for on an ongoing basis as our client portfolio grows.

Full-time / contract

Cosmetic Regulatory Consultant

Manages client projects end to end across one or more markets.

  • PIF/CPSR coordination, CPNP/SCPN notifications
  • MoCRA facility registration and product listing
  • Formula, INCI and label reviews
Entry level

Regulatory Associate

Supports consultants on dossiers, screenings and submissions.

  • Ingredient screening against annexes and restricted lists
  • Health Canada CNF and portal submissions
  • Document control and client follow-up
Freelance

Safety Assessor / Toxicologist

Qualified assessors for EU and UK cosmetic product safety reports.

  • CPSR Part B sign-off (Article 10 qualification)
  • MoS calculations and toxicological profiles
  • Fragrance and allergen assessments
Full-time / contract

Food, Supplement & OTC Specialist

Regulatory support beyond cosmetics for US and Canadian markets.

  • FDA food facility registration and FSVP
  • DSHEA claims and NHP/NPN applications
  • OTC monograph and Drug Facts labelling
What we look for

Skills that make a difference

  • A degree in chemistry, pharmacy, biology, toxicology, food science or a related field
  • Hands-on experience with at least one framework: EU/UK cosmetics, FDA, Health Canada or UAE
  • Clear, professional written English; extra languages are a plus
  • Precision with documents, deadlines and version control
  • Discretion with confidential client information and formulations

How we work

  • Office-based or hybrid arrangements, depending on role and location
  • Documented procedures, templates and project tracking
  • Four-eyes review on every regulatory deliverable
  • Strict confidentiality of client data, formulations and dossiers
  • Structured onboarding and ongoing regulatory training
Our footprint

One team, five regulatory regions

Since 2013Regulatory affairs consulting
5 regionsUS · EU · UK · Canada · UAE
5 sectorsCosmetics, OTC, food, supplements, devices
10+ languagesAcross our website and client work
Hiring process

What happens after you apply

Application

Submit your CV with details of your regulatory experience and qualifications.

Review

Our team reviews each profile and keeps qualified candidates on file for future roles.

Interview

Interviews with our regulatory team, followed by a technical assessment.

Onboarding

Structured onboarding on our procedures, with a senior consultant assigned to your first projects.

Are there vacancies open at the moment?
We are not advertising specific vacancies at present. Qualified candidates can submit their CV and we will contact them when a suitable position opens.
Where are roles based?
It depends on the role. Positions are office-based or hybrid, linked to our locations in the United States, United Kingdom, Ireland and the UAE. Some specialist roles can be carried out remotely.
Do you offer freelance or part-time work?
For specific profiles, such as qualified safety assessors and toxicologists, we work with experienced professionals on a contract basis.
Do you hire graduates?
Yes, for associate roles. A relevant scientific degree and a genuine interest in regulatory affairs matter more than years of experience.
How long do you keep my CV?
We keep applications only for recruitment purposes and for a limited period, in line with our privacy policy. You can ask us to delete your data at any time.

Submit your CV

Share your CV and details of your regulatory experience, the markets you know and the languages you work in. We will contact you when a suitable position opens.

Cosmereg is an equal-opportunity employer. We welcome applications from all backgrounds.
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