... Label Working Group) * Provide functional area input for Global Regulatory Plan and team goals * Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
... Label Working Group) * Provide functional area input for Global Regulatory Plan and team goals * Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
Regulatory Writing Sr Mgr
Washington, DC · On-site +1
... Label Working Group) * Provide functional area input for Global Regulatory Plan and team goals * Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
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Regulatory Writing Sr Mgr
Washington, DC · On-site +1
... Label Working Group) * Provide functional area input for Global Regulatory Plan and team goals * Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
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Regulatory Writing Sr Mgr
Washington, DC · On-site +1
... Label Working Group) * Provide functional area input for Global Regulatory Plan and team goals * Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
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Regulatory Writing Sr Mgr
Washington, DC · On-site +1
... Label Working Group) * Provide functional area input for Global Regulatory Plan and team goals * Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
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Senior Graphic Designer
Patchogue, NY · On-site
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... freelancers, agency partners, and junior designers with constructive feedback. * Maintain organized, well-named working files and an asset library. * Route work through legal/regulatory/label ...
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... Label Working Group) * Provide functional area input for Global Regulatory Plan and team goals * Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
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Freelance Senior Production Artist (Packaging)
Providence, RI · On-site
$35 - $42.50/hr
Packaging design experience in private label health care and personal care strongly preferred ... Regulatory/Compliance, Proofreaders and Senior Quality Manager in the development of all artwork ...
New
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Data Security & DLP Analyst
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Lead packaging and label design from concept through final production * Manage packaging and ... Ensure compliance with regulatory and production requirements where applicable Campaign & Brand ...
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Lead packaging and label design from concept through final production * Manage packaging and ... Ensure compliance with regulatory and production requirements where applicable Campaign & Brand ...
$100 - $120/hr
You'll be writing and editing regularly while also directing a roster of freelance writers and an ... Collaborate closely with our regulatory team to ensure all copy meets guidelines without ...
New
$100 - $120/hr
You'll be writing and editing regularly while also directing a roster of freelance writers and an ... Collaborate closely with our regulatory team to ensure all copy meets guidelines without ...
New
Master Electrician
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$121.77 - $129.15/hr
Attend the electrical equipment vendor location, October 27‑29, 2026 to verify, label, test ... We partner with elite, safety‑first freelancers to execute high‑profile experiential builds ...
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Master Electrician
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$121.77 - $129.15/hr
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Supporting fabric compliance, testing, and regulatory requirements throughout development and ... freelancers - which sets us apart in the industries we serve. About Solomon Page Founded in 1990 ...
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$60K - $80K/yr
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Senior Graphic Designer
Patchogue, NY · On-site
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Patchogue, NY · On-site
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Senior Graphic Designer
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Senior Graphic Designer
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Senior Graphic Designer
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Senior Graphic Designer
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Senior Graphic Designer
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Senior Graphic Designer
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Freelance Regulatory Labeling information
See salary details
$23.52 is the 25th percentile. Wages below this are outliers.
$14.90 - $25.57
31% of jobs
The median wage is $32.14 / hr.
$25.57 - $36.23
31% of jobs
$36.23 - $46.90
4% of jobs
$56.23 is the 75th percentile. Wages above this are outliers.
$46.90 - $57.56
10% of jobs
$57.56 - $68.23
9% of jobs
$68.23 - $78.89
5% of jobs
$78.89 - $89.55
0% of jobs
$89.55 - $100.22
8% of jobs
$100.22 - $110.88
0% of jobs
$110.88 - $121.55
0% of jobs
$121.55 - $132.21
1% of jobs
$14
$47
$132
How much do freelance regulatory labeling jobs pay per hour?
What is the difference between Freelance Regulatory Labeling vs Regulatory Affairs Specialist?
| Aspect | Freelance Regulatory Labeling | Regulatory Affairs Specialist |
|---|---|---|
| Credentials | Typically requires knowledge of labeling regulations, certifications vary | Requires degrees in life sciences or related fields, certifications like RAC |
| Work Environment | Independent, project-based, remote or contract work | In-house or consulting roles within companies or agencies |
| Industry Usage | Common in pharmaceutical, medical device, and consumer health industries | Standard role in regulatory departments of healthcare companies |
Freelance Regulatory Labeling professionals focus on creating and reviewing product labels on a contract basis, often working remotely. Regulatory Affairs Specialists typically hold full-time positions within organizations, managing broader regulatory strategies. Both roles require knowledge of industry regulations, but Freelance Regulatory Labeling offers more flexibility, while Regulatory Affairs Specialists have a more comprehensive regulatory scope.
What cities are hiring for Freelance Regulatory Labeling jobs?
Cities with the most Freelance Regulatory Labeling job openings:
What are the most commonly searched types of Regulatory Labeling jobs?
The most popular types of Regulatory Labeling jobs are:
What states have the most Freelance Regulatory Labeling jobs?
States with the most job openings for Freelance Regulatory Labeling jobs include:
What job categories do people searching Freelance Regulatory Labeling jobs look for?
The top searched job categories for Freelance Regulatory Labeling jobs are:

Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 10 days ago
Job description
Regulatory
Job Description
Job Description
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of.
Regulatory Writing Senior Manager
Live
What you will do
Let's do this. Let's change the world. In this key role you will serve as the functional area lead on product teams, lead writing activities for complex product submissions, provide functional area expertise, train and mentor more junior writers, and lead departmental activities. Key responsibilities include:
- Author or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, and Pediatric Investigation Plans
- Conduct the formal review and approval of authored documents, following applicable standard operating procedures
- With limited supervision, lead regulatory writing activities for complex product submissions, including new and supplemental drug applications/biologics license applications
- Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
- Provide functional area input for Global Regulatory Plan and team goals
- Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
- Lead departmental and cross-departmental initiatives, as appropriate
- Generate document timelines
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.
Basic Qualifications:
Doctorate degree and 2 years of directly related experience
OR
Master's degree and 6 years of directly related experience
OR
Bachelor's degree and 8 years of directly related experience
OR
Associate's degree and 10 years of directly related experience
Or
High school diploma / GED and 12 years of directly related experience
Preferred Qualifications:
- Experience with regulatory documents in Regulatory Affairs, Research, Development or related area
- 5+years of experience in medical writing in the Biotech/Pharmaceutical industry
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being.
Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:
- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans and bi-annual company-wide shutdowns
- Flexible work models, including remote work arrangements, where possible
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Salary Range
139,581.90USD -188,846.10 USD