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Entry Level Cosmetics Regulatory Jobs (NOW HIRING)

Entry Level Chemist- Package Testing

Lancaster, PA · On-site

$21.50 - $28.75/hr

... cosmetic product testing and in agroscience Contract Research Organization services. It is one of ... regulations. Essential Duties and Responsibilities: * Applies GMP/GLP in all areas of ...

Assembly B

Londonderry, NH

$16.50 - $19.25/hr

... cosmetic requirements. Continuously perform visual inspections of materials for defects and ... entry-level soldering

Manufacturing Assembly

Golden, CO · On-site

$17 - $21/hr

Past experience in Cosmetic Finishing, requiring a high attention to detail Key responsibilities ... Comply with EHS regulations and policies Additional Information CONTACT: Anil Kumar 703-230-2657

Use grinding and sanding tools to repair cosmetic damages (curb and road rash, peeling, scrapes ... and regulations. The compensation offered for this position will depend on qualifications ...

Assembly B

Londonderry, NH · On-site

$18.25 - $23/hr

... cosmetic requirements. * Continuously performs visual inspections of materials for defects and ... Perform job duties in a manner that complies with environmental, health and safety regulations ...

Showing results 41-60

Entry Level Cosmetics Regulatory information

See salary details

$34K

$59K

$114.5K

How much do entry level cosmetics regulatory jobs pay per year?

As of Aug 23, 2026, the average yearly pay for entry level cosmetics regulatory in the United States is $58,981.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $77,000.00 per year, depending on experience, location, and employer.

What is an entry level cosmetics regulatory professional?

Entry level cosmetics regulatory jobs are positions where individuals assist in ensuring that cosmetic products comply with all relevant government regulations and industry standards. These roles typically involve reviewing product labels and ingredients, preparing documentation for regulatory submissions, and staying up-to-date on changes in cosmetic regulations. Entry level professionals often work under supervision and may interact with product development, quality assurance, and marketing teams to help bring safe and legal products to market.

What are the key skills and qualifications needed to thrive as an entry level cosmetics regulatory professional?

To thrive as an Entry Level Cosmetics Regulatory professional, you need a foundational understanding of cosmetic regulations, scientific principles, and attention to detail, typically supported by a degree in chemistry, biology, or a related field. Familiarity with regulatory databases, product labeling software, and documentation systems is often required. Strong communication, organization, and problem-solving skills help you interpret guidelines and collaborate with cross-functional teams. These competencies are vital to ensure products comply with legal standards, avoid costly recalls, and maintain consumer trust.

What are some common challenges faced by entry level cosmetics regulatory professionals?

Entry-level professionals in cosmetics regulatory roles often encounter challenges such as interpreting evolving regulations, learning to navigate complex documentation requirements, and ensuring product compliance across different markets. Adapting to the fast pace of regulatory updates and collaborating with cross-functional teams (like product development, marketing, and quality assurance) can also be demanding. However, these challenges provide excellent learning opportunities and pave the way for growth into more specialized or senior regulatory positions.

What is the difference between Entry Level Cosmetics Regulatory vs Entry Level Quality Assurance Specialist?

AspectEntry Level Cosmetics RegulatoryEntry Level Quality Assurance Specialist
Required CredentialsCosmetics-related certifications, basic regulatory knowledgeQuality assurance certifications, understanding of standards
Work EnvironmentRegulatory agencies, cosmetics companiesManufacturing plants, product testing labs
Employer & Industry UsageCosmetics and personal care industryManufacturing and production sectors
Common Search & Comparison IntentUnderstanding regulatory roles in cosmeticsUnderstanding quality assurance roles in manufacturing

Entry Level Cosmetics Regulatory focuses on ensuring cosmetic products comply with regulations, while Entry Level Quality Assurance Specialist emphasizes maintaining product quality standards. Both roles are essential in the cosmetics industry but differ in their primary responsibilities and focus areas.

More about Entry Level Cosmetics Regulatory jobs

What cities are hiring for Entry Level Cosmetics Regulatory jobs?

Cities with the most Entry Level Cosmetics Regulatory job openings:

What are the most commonly searched types of Cosmetics Regulatory jobs?

The most popular types of Cosmetics Regulatory jobs are:

Infographic showing various Entry Level Cosmetics Regulatory job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 9% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $58,981 per year, or $28.4 per hour.

Entry Level Chemist- Package Testing

Eurofins

Lancaster, PA • On-site

$21.50 - $28.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

67th of 120 rated laboratories


Job description

Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
**Please note this position is a 4/10 schedule on 2nd or 3rd shift**
Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
Essential Duties and Responsibilities:
  • Applies GMP/GLP in all areas of responsibility, as appropriate
  • Applies the highest quality standard in all areas of responsibility
  • Demonstrates and promotes the company vision
  • Demonstrates strong client service skills, teamwork, and collaboration
  • Proactively plans and multitasks to maximize productivity
  • Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
  • Regular attendance and punctuality
  • Performs laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precision
  • Perform/Review preparations of reagents, samples, and standards according to procedures.
  • Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors
  • Understand and perform calculations as required by test methods
  • Understand and utilize computers for information access, calculations, and report preparation
  • Read and understand analytical procedures (compendial and client supplied) and internal SOP's
  • Use MS Windows applications such as Excel, Word, Outlook email
  • Process data, generate reports, and evaluate data
  • Communicate effectively, both orally and in writing
  • Independently seek out work
  • Perform laboratory maintenance
  • Commitment to occasional overtime as workload requires
  • Conducts all activities in a safe and efficient manner
  • Ensures good housekeeping with a neat, clean and orderly workspace
  • Performs other duties as assigned
  • Communicates effectively with client staff members

Qualifications
Minimum Qualifications:
  • Bachelor's degree in microbiology, biology, biochemistry, or related degree concentration and no industry laboratory experience
  • Authorized to work in the US INDEFINITELY without restriction or sponsorship
  • Microbiology lab skills; pipetting, microscopes, staining, plating, etc.
  • Med device experience is a plus

Additional Qualifications:
  • Good dexterity, positive attitude, solution driven
  • good work habits (organized, efficient, careful, safety-concious, accurate)
  • attention to detail
  • sound scientific logic
  • good oral and written communication skills
  • understanding of instrumentation
  • client service focused
  • demonstration of organizational skills
  • ability to work with moderate supervision upon training completion on assigned task
  • ability to handle multitasking

Additional Information
Working schedule will be Full-Time, Second or Third Shift, Sun-Wed or Wed-Sat, 2pm-12am or 12am-10am. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is NOT remote.
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA Medical Devices is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US