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Regulatory Affairs In Cosmetics Jobs (NOW HIRING)

LifeWave

Regulatory Affairs Manager - EMEA

Draper, UT · On-site

POSITION SUMMARY Regulatory Affairs Manager - EMEA for EMEA region responsible for all things ... Experience in cosmetics and dietary supplement contract manufacturing plus * Proficiency in ...

LifeWave

Regulatory Affairs Manager - EMEA

Draper, UT · On-site

POSITION SUMMARY Regulatory Affairs Manager - EMEA for EMEA region responsible for all things ... Experience in cosmetics and dietary supplement contract manufacturing plus * Proficiency in ...

Club Kuma

Regulatory Affairs Specialist

Santa Monica, CA · On-site

$80K - $100K/yr

Must-haves: * 3-5 years in Regulatory Affairs, ideally in cosmetics or personal care * Working knowledge of U.S. cosmetic regulations, including MoCRA * Experience reviewing formulas, ingredients ...

Legend Biotech US

Director, Regulatory Affairs

Somerset, NJ · Hybrid

$158K - $209K/yr

Legend Biotech is seeking a Director, Regulatory Affairs as part of the Regulatory Affairs team based in Somerset, NJ. Role Overview The Director of Regulatory Affairs is responsible for ...

Sigan America LLC

Regulatory Affairs Specialist

Ottawa, IL · On-site

$70K - $100K/yr

Bachelor's degree in Chemistry, Biology, Regulatory Science, Pharmaceutical Sciences, or a related scientific discipline. * 2-4 years of Regulatory Affairs experience within cosmetics, personal care ...

Legend Biotech US

Director, Regulatory Affairs

Somerset, NJ · On-site

$158K - $209K/yr

Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy ... Role Overview The Director of Regulatory Affairs is responsible for independently developing ...

Legend Biotech USA, Inc.

$158K - $209K/yr

Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy ... Role OverviewThe Director of Regulatory Affairs is responsible for independently developing ...

MWI Animal Health

NY · On-site

## Regulatory Affairs ManagerPostulerlocations: NCEE > Poland > Remotetime type: Temps Pleinposted on ... in Poland* Experience with adjacent product categories such as medical devices, cosmetics, food ...

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Regulatory Affairs In Cosmetics information

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$15

$34

$145

How much do regulatory affairs in cosmetics jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for regulatory affairs in cosmetics in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What is the difference between Regulatory Affairs In Cosmetics vs Quality Assurance Specialist in Cosmetics?

AspectRegulatory Affairs In CosmeticsQuality Assurance Specialist in Cosmetics
Required CredentialsDegree in life sciences, certifications in regulatory affairsDegree in sciences, certifications in quality management
Work EnvironmentRegulatory agencies, R&D, compliance departmentsManufacturing plants, quality control labs
Employer & Industry UsageCosmetic companies, regulatory bodiesCosmetic manufacturing, quality assurance firms
Common Search & ComparisonYesYes

Regulatory Affairs In Cosmetics focuses on ensuring products meet legal and regulatory standards, handling documentation and compliance. Quality Assurance Specialists in Cosmetics concentrate on maintaining product quality, testing, and process improvements. While both roles support product safety, Regulatory Affairs In Cosmetics primarily manages compliance with regulations, whereas Quality Assurance Specialists focus on product quality control throughout manufacturing.

What cities are hiring for Regulatory Affairs In Cosmetics jobs?

Cities with the most Regulatory Affairs In Cosmetics job openings:

What states have the most Regulatory Affairs In Cosmetics jobs?

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What are popular job titles related to Regulatory Affairs In Cosmetics jobs?

For Regulatory Affairs In Cosmetics jobs, the most frequently searched job titles are:

Regulatory Affairs In Cosmetics jobs near you
Infographic showing various Regulatory Affairs In Cosmetics job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 8% Part Time, and 3% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Regulatory Affairs Manager - EMEA

Draper, UT • On-site

LifeWave
See more jobs at LifeWaveexternal

Other

Re-posted 6 days ago

Job description

Job Description
Job Description

POSITION SUMMARY

Regulatory Affairs Manager – EMEA for EMEA region responsible for all things Regulatory in the region, including but not limited to ingredient review, marketing collateral review, product registrations, and label reviews. Understands, implements, and maintains the quality policy. Ensures compliance to and demonstrates knowledge of site and division-level policies and procedures.

SUPERVISORY RESPONSIBILITIES

This position has supervisory responsibilities for this role.

Title(s):

  • Regulatory Affairs Supervisor - APAC

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Provide day-to-day leadership, coaching, and performance management for the Regulatory Affairs Specialist, ensuring high-quality regulatory deliverables, professional development, and alignment with departmental objectives.
  • Review and prioritize the Regulatory Affairs Specialist’s workload, ensuring timely execution of regulatory submissions, compliance activities, and regulatory documentation in accordance with business and regulatory requirements.
  • Assist Sr. Director – Global RA responsibilities to manage department tasks and staff.
  • Responsible for reulatory activities of LW EMEA countries to launch and secure the products in the markets.
  • Basic understanding of laws and regulations of the responsible EMEA countries.
  • Assisting the department head in responding to all product-related inquiries and actions by regulators and internal departments.
  • Assisting in preparing and filing necessary documentation for applications with international government agencies for product registration and coordinating advice on technical aspects of product labeling, product dossiers, claims substantiation/localization, and product registrations.
  • Reviewing marketing materials for compliance with advertising law and scientific substantiation.
  • Reviewing product labels for compliance with local labeling regulations for medical devices, general wellness, supplements, and cosmetics.
  • Manage Regulatory tools and trackers.
  • Perform other related duties assigned by department head.
  • Obtains supervisory regulatory review on submission documents before submission to government agencies.
  • Signs off at the team level within delegated parameters for change control.
  • Releases authority for labeling/sales/promotional materials.
  • Share knowledge with others in the department.

QUALIFICATIONS AND EXPERIENCE

  • Bachelor's degree in business or related field or 7-9 years of experience in regulatory affairs in medical device, cosmetic, food, and dietary supplement field in EMEA. Experience in cosmetics and dietary supplement contract manufacturing plus
  • Proficiency in Microsoft Suite required.
  • Strong attention to detail and time management skills.
  • Excellent communication skills, both written and oral.
  • High level of observation must be able to learn quickly with an ability to be self-sufficient, motivated and to work independently.
  • Bilingual proficiency is preferred but not required.

Work Environment & Physical Demands

LifeWave will operate as an in-office organization, and all employees are required to work onsite in alignment with corporate policy. While performing the duties of this job, the employee is regularly required to work at a computer workstation and be mobile within the office. Occasional movement of up to 25 pounds may be required.

LifeWave is committed to creating an inclusive workplace that values diversity and promotes equal opportunities for all. We embrace the principles of the Americans with Disabilities Act (ADA) and strive to provide reasonable accommodations to qualified individuals with disabilities.

In our pursuit of building a diverse and talented team, we encourage candidates of all abilities to apply for positions at LifeWave. If you require accommodation during the application or interview process, please inform our HR department, and we will work with you to ensure your needs are met.

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