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Remote Cosmetic Regulatory Jobs (NOW HIRING)

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc... * Respond to the ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc... * Respond to the ...

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc... * Respond to the ...

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Remote Cosmetic Regulatory information

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$13

$52

$70

How much do remote cosmetic regulatory jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for remote cosmetic regulatory in the United States is $52.19, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $63.46 per hour, depending on experience, location, and employer.

What is a remote cosmetic regulatory job?

Remote cosmetic regulatory jobs involve overseeing and ensuring that cosmetic products comply with local, national, and international regulations, but the work is performed from a remote location rather than an office. Professionals in this field review product formulations, labels, packaging, and marketing materials to ensure compliance with safety standards and legal requirements. They may also interact with regulatory agencies, provide guidance to product development teams, and keep up with evolving cosmetic laws. Remote roles offer flexibility and allow experts to collaborate with companies across various regions without being physically present in an office.

What are some common challenges faced by professionals in remote cosmetic regulatory roles, and how can they be addressed?

Remote cosmetic regulatory professionals often face challenges such as staying current with frequently changing international regulations, managing documentation across multiple platforms, and ensuring clear communication with cross-functional teams in different time zones. To address these, it's important to regularly participate in industry webinars, subscribe to regulatory updates, and use reliable document management systems. Building strong digital communication habits and scheduling regular check-ins with team members can also help maintain clarity and collaboration.

What are the key skills and qualifications needed to thrive as a remote cosmetic regulatory professional, and why are they important?

To excel as a Remote Cosmetic Regulatory professional, you need a strong background in regulatory affairs, chemistry, or life sciences, along with in-depth knowledge of global cosmetic regulations and compliance standards. Familiarity with regulatory databases, labeling software, and document management systems, as well as certifications like RAC (Regulatory Affairs Certification), are often required. Exceptional attention to detail, strong written communication, and the ability to collaborate across remote teams are vital soft skills. These competencies ensure accurate compliance, minimize legal risks, and facilitate the timely launch of cosmetic products in various markets.

What is the difference between Remote Cosmetic Regulatory vs Remote Cosmetic Product Development Specialist?

AspectRemote Cosmetic RegulatoryRemote Cosmetic Product Development Specialist
CredentialsRegulatory certifications, such as CCRA or similarProduct formulation and development certifications, e.g., CID, CTP
Work EnvironmentRegulatory compliance, documentation, legal standardsFormulation, testing, product design
Employer & Industry UsageCosmetic companies, regulatory agencies, consulting firmsCosmetic brands, R&D labs, manufacturing firms
Search & Comparison IntentUnderstanding regulatory roles, compliance tasksProduct creation, formulation processes

Remote Cosmetic Regulatory professionals focus on ensuring products meet legal standards and compliance requirements, while Remote Cosmetic Product Development Specialists concentrate on creating and formulating new cosmetic products. Both roles are essential in the cosmetics industry but differ in their core responsibilities and skill sets.

More about Remote Cosmetic Regulatory jobs

What cities are hiring for Remote Cosmetic Regulatory jobs?

Cities with the most Remote Cosmetic Regulatory job openings:

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

The most popular types of Cosmetic Regulatory jobs are:

What states have the most Remote Cosmetic Regulatory jobs?

States with the most job openings for Remote Cosmetic Regulatory jobs include:

Infographic showing various Remote Cosmetic 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 $108,557 per year, or $52.2 per hour.

Corporate Counsel, Global Legal Technical Operations & Facilities

Genentech

South San Francisco, CA • On-site, Remote

$181K - $337K/yr

Full-time

Re-posted 22 days ago


Genentech rating

8.8

Company rating: 8.8 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

Great medicine can't change the world if it never leaves the lab. Our Pharma Technical Operations (PT) organization is the global backbone that transforms scientific discoveries into real-world therapies. Joining our Global Legal Technical Operations & Facilities team means stepping onto a highly collaborative, global team of experts. Together, we provide the proactive legal support that empowers PT to manufacture and deliver medicines safely and efficiently. You'll be trusted to advise on complex, high-stakes matters, knowing that your daily work supports our patients and our company's global ambition to prevent, stop and cure diseases.

We are seeking to hire a Corporate Counsel in Global Legal Technical Operations & Facilities. This team member will focus on global support to PT and its sites involving regulatory and transactional counseling on environmental, health & safety matters, FDA/cGMP, manufacturing supply and development agreements, and other related matters.

The Opportunity

Key responsibilities of this individual contributor role may include but not be limited to the following:

  • Providing legal advice and strategic counseling to PT sites, Environmental Health and Safety (EHS) departments, global EHS functions, and other business units.

  • Advising and representing our manufacturing sites on EHS compliance and enforcement matters, sustainability, and environmental land use issues.

  • Coordinating environmental due diligence; drafting and negotiating EHS and related provisions of contracts; and counseling on environmental site remediation.

  • Advising on regulatory and compliance matters arising under the Federal Food, Drug, and Cosmetic Act related to manufacturing practices (cGMP), quality system requirements, and other issues and agreements involving quality considerations.

  • Preparing and negotiating manufacturing supply and development agreements, and advising on related transactional issues key to manufacturing operations.

  • Managing outside counsel retained to support legal matters.

The How

Legal excellence accelerates in combination with the right business- and solutions-focused attitude, mindset, and ways of working. Here is who we are looking for:

Communication and Leadership

  • Pro-active and confident individual who is committed to driving change.

  • Strong verbal and written communication skills.

  • Ability to communicate complex and highly technical information clearly and concisely.

  • Commitment to working as a team player in a multinational legal department.

  • Excellent interpersonal skills with high cross-cultural sensitivity.

  • Willingness to travel.

Our Expectations

  • Strong business acumen; sensitive to business needs; views change as an opportunity; eager to work in a fast paced environment.

  • Best in class attitude; challenges status quo constructively and contributes to improvements; results oriented; ability to influence; solutions oriented mindset.

Who You Are

  • 5+ years of EHS or manufacturing related legal experience, ideally in a pharma/biotech corporate setting and/or in a law firm or relevant government agency.

  • A U.S. law degree (J.D.) and current "good standing" admission to at least one U.S. state bar, or be eligible to apply to California's Registered In-House Counsel program.

  • Demonstrated experience and track record of success or committed interest in:

    • Providing EHS regulatory compliance advice to industrial clients, preferably to the pharmaceutical or biotech industries;

    • Providing manufacturing support in pharmaceutical or biotech industries, such as regulatory counseling on FDA/cGMP related matters.

Location

  • This role is located at Genentech's South San Francisco, California campus. A remote working arrangement is not available.

  • Relocation benefits are not available for this position.

The expected salary range for this position based on the primary location of California is$181,800 to $337,600. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

Benefits

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.


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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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