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Regulatory Affairs Writer Jobs (NOW HIRING)

5TH HQ LLC

Regulatory Affairs

Plantation, FL · On-site

$19 - $20/hr

If you are passionate about regulatory affairs and looking for an opportunity to grow within a ... Effective communication skills, both written and verbal. * Proficiency in Microsoft Office Suite ...

Precigen, Inc

Manager, Regulatory Writing

Germantown, MD · On-site

$100K - $120K/yr

Reporting to the SVP, Regulatory Affairs, this role will work cross functionally to provide writing support in the creation of effective and timely communications that meet all applicable regulatory ...

Zymo Research

Regulatory Affairs Associate

Tustin, CA · On-site

$68K - $75K/yr

Research applicable regulations, standards, and guidance documents and summarize findings for review * Assist with reviewing and writing SOPs and other Regulatory Affairs policies as necessary

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Regulatory Affairs Writer information

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$34

$145

How much do regulatory affairs writer jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for regulatory affairs writer 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 Writer vs Regulatory Affairs Specialist?

AspectRegulatory Affairs WriterRegulatory Affairs Specialist
CredentialsBachelor's degree, writing certifications often preferredBachelor's degree, often with regulatory or science certifications
Work EnvironmentPrimarily office-based, focused on document creationOffice and lab settings, involved in compliance and submissions
Industry UsageUsed across pharmaceutical, biotech, medical device companiesCommon in similar industries, with broader regulatory responsibilities
Search/Comparison IntentHigh overlap in skills and industry, often compared for clarity

While both roles operate within regulatory environments, a Regulatory Affairs Writer primarily focuses on creating clear, compliant documentation, whereas a Regulatory Affairs Specialist handles broader regulatory activities, including submissions and compliance management. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Regulatory Affairs Writer jobs?

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

Infographic showing various Regulatory Affairs Writer 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 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Regulatory Affairs Medical Writer

Bethlehem, PA • On-site

Exalta Group
See more jobs at Exalta Groupexternal

Full-time

Re-posted 23 days ago

Job description

Position Summary

We are seeking an experienced Medical Writer / Regulatory Affairs Specialist to lead the preparation and maintenance of Clinical Evaluation Reports (CERs), Periodic Safety Update Reports (PSURs), and Summary of Safety and Clinical Performance (SSCPs) for our orthopedic device portfolio, including implants and surgical instrumentation.

This role is critical to ensuring compliance with EU MDR (2017/745) and supporting the clinical and regulatory strategy for joint reconstruction, spine, trauma, and/or extremities products

This role will collaborate cross-functionally with Clinical, Product Development, Regulatory, Quality, and Post-Market Surveillance teams to ensure high-quality documentation supporting product safety, performance, and regulatory compliance throughout the product lifecycle.

Key Responsibilities

Clinical Evaluation Documentation

  • Author, update, and maintain Clinical Evaluation Reports (CERs) for orthopedic implants and instruments in accordance with EU MDR and MEDDEV 2.7/1 Rev. 4.
  • Perform systematic literature reviews, clinical data appraisal, and benefit-risk analyses.
  • Ensure clinical evidence supports device safety and performance claims.

Post-Market Surveillance & Safety Reporting

  • Prepare and maintain Periodic Safety Update Reports (PSURs) per MDR requirements for Class Ir, IIa, IIb, and III orthopedic devices.
  • Analyze post-market data including complaints, vigilance, and PMS data to identify trends.
  • Contribute to signal detection, risk assessment, and updates to risk management files.

SSCP Development

  • Prepare and maintain Summary of Safety and Clinical Performance (SSCP) documents for implantable and Class III orthopedic devices.
  • Translate complex clinical and safety information into clear, patient-friendly summaries.
  • Interface with Notified Bodies for SSCP review, approval, and EUDAMED submission readiness.

Cross-Functional Collaboration

  • Collaborate with Clinical Affairs, Product Development, Quality, Regulatory Affairs, and Post-Market Surveillance teams to gather necessary inputs.
  • Ensure alignment between CERs, Risk Management Files, PMS reports, and labeling. 
  • Support internal and external audits, including Notified Body inspections.
  • Contribute to regulatory submissions and lifecycle management activities.

Qualifications

Education

  • Bachelor’s or advanced degree in Life Sciences, Biomedical Engineering, Pharmacy, or a related field.

Experience


  • 5+ years in medical writing, clinical evaluation, or regulatory affairs within the medical device industry
  • Direct experience authoring: CERs, PSURs, and SSCPs
  •  Strong experience with orthopedic devices (e.g., joint replacement, trauma, spine, sports medicine) strongly preferred
  • Strong understanding of: 
    • EU MDR (2017/745)
    • MEDDEV 2.7/1 Rev. 4
    • MDCG guidance documents
    • ISO 14155, ISO 14971, ISO13485 (preferred)

Skills & Competencies

  • Detail-oriented with strong organizational skills 
  • Ability to manage multiple complex products and deadlines
  • Excellent scientific writing, editing, and critical appraisal skills.
  • Strong analytical ability to interpret clinical and safety data.
  • Knowledge of literature search methodologies and databases (e.g., PubMed, Embase).
  • Attention to detail and ability to manage multiple projects simultaneously.
  • Strong communication and stakeholder management skills.
  • Proficiency in MS Office and document management systems.

Preferred Qualifications

  • Experience working with Notified Bodies and regulatory submissions in Europe.
  • Familiarity with global regulatory frameworks (FDA, Health Canada, etc.).
  • Experience in specific therapeutic areas (e.g., cardiovascular, orthopedics, diagnostics).

Work Environment

  • Cross-functional, collaborative environment.
  • Hybrid, or office-based position



EXALTA is an Equal Opportunity Employer. We respect every employee as an individual, and we hire and promote based on qualifications, performance, and potential - without regard to race, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.