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Qa Medical Editor Jobs (NOW HIRING)

Initial Therapeutics, Inc.

NY · On-site

$126K - $206K/yr

Regeneron is currently seeking a Senior Manager, Medical Device Quality Assurance (QA) to join our Medical Device QA team. This expanded leadership role will provide QA oversight across two critical ...

Ketryx

QA/RA Consultant

Boston, MA · On-site +1

$130K - $150K/yr

Job Title: QA/RA Consultant Employment Status: Full-time Office Hours: Monday - Friday; hybrid ... You've built or significantly improved quality systems at medical device companies, consulting ...

AVANTech, LLC

Quality Assurance Associate II

Columbia, SC · On-site

$22 - $27/hr

Excellent written communication skills for editing, summarizing, or compiling information clearly ... Medical, dental, vision, disability, and life insurance with employer contributions. * 401(k) ...

AVANTech, LLC

Quality Assurance Associate II

Columbia, SC · On-site

$22 - $27/hr

Excellent written communication skills for editing, summarizing, or compiling information clearly ... Medical, dental, vision, disability, and life insurance with employer contributions. * 401(k) ...

Ketryx

QA/RA Consultant

Boston, MA · On-site

$130K - $150K/yr

Job Title: QA/RA Consultant Employment Status: Full-time Office Hours: Monday - Friday; hybrid ... You've built or significantly improved quality systems at medical device companies, consulting ...

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Qa Medical Editor information

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How much do qa medical editor jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for qa medical editor in the United States is $41.22, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $50.24 per hour, depending on experience, location, and employer.

What is a QA medical editor?

QA Medical Editors are professionals who review and ensure the accuracy, consistency, and quality of medical documents, such as research articles, clinical study reports, and regulatory submissions. They check for grammatical errors, adherence to style guides, and correct use of medical terminology. Additionally, QA Medical Editors verify that the content complies with regulatory standards and guidelines, ensuring clarity and precision in all medical communications. Their work is crucial in maintaining the credibility and integrity of medical information.

What are the key skills and qualifications needed to thrive as a QA medical editor?

To thrive as a QA Medical Editor, you need a solid background in medical terminology, scientific writing, and quality assurance processes, often supported by a degree in life sciences or a related field. Familiarity with editing tools (such as Microsoft Word with track changes), reference management systems, and standards like AMA or ICMJE guidelines is typically required. Exceptional attention to detail, strong organizational skills, and effective communication are vital soft skills in this role. These competencies ensure the accuracy, consistency, and compliance of medical documents, which is critical for regulatory submissions and maintaining high editorial standards.

What are the main challenges faced by QA medical editors when reviewing clinical documents?

QA Medical Editors often encounter challenges such as ensuring consistency with medical terminology, verifying data accuracy, and maintaining compliance with regulatory guidelines. They must carefully check for errors in grammar, formatting, and scientific content while meeting tight deadlines. Collaboration with medical writers, researchers, and regulatory teams is also essential to clarify ambiguities and address complex edits, making communication and attention to detail vital skills in this role.

What is the difference between Qa Medical Editor vs Medical Writer?

AspectQa Medical EditorMedical Writer
CredentialsTypically requires a medical degree or related certification, editing experienceUsually holds a medical, scientific, or healthcare degree, with writing experience
Work EnvironmentWorks in regulatory, pharmaceutical, or healthcare companies, focusing on editingWorks in publishing, healthcare communication, or pharmaceutical industries, focusing on writing
Employer & Industry UsageCommonly employed by pharma, biotech, or regulatory agenciesEmployed by publishers, agencies, or healthcare companies

In summary, Qa Medical Editors focus on reviewing and ensuring the accuracy of medical content, often requiring editing skills and medical credentials. Medical Writers primarily create and develop medical content, emphasizing writing skills and subject matter expertise. Both roles are vital in healthcare communication but differ in their core responsibilities and skill sets.

What are popular job titles related to Qa Medical Editor jobs?

For Qa Medical Editor jobs, the most frequently searched job titles are:

Infographic showing various Qa Medical Editor job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $85,736 per year, or $41.2 per hour.

Senior Manager Quality Assurance, Medical Device (Sustaining)

NY • On-site

Initial Therapeutics, Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about Initial Therapeutics, Inc.external

$126K - $206K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago

Key responsibilities

  • Manage, mentor, and develop quality engineering and compliance teams

  • Standardize, streamline, and improve processes across sustaining and compliance

  • Support sustaining engineering programs through risk assessment, design change management, and maintenance of documentation

Job description

Build our future together:

Regeneron is currently seeking a Senior Manager, Medical Device Quality Assurance (QA) to join our Medical Device QA team. This expanded leadership role will provide QA oversight across two critical functions: Combination Products Sustaining Engineering and Compliance. The position will lead a team of engineers and quality specialists.

When & where:
  • Location: East Greenbush, New York, United States
  • Work model: Monday-Friday, 8am-4:30pm
Discover your role:
  • Manage, mentor, and develop quality engineering and compliance teams
  • Standardize, streamline, and improve processes across sustaining and compliance
  • Implement digital, data-driven tools for accurate, consistent, and timely reporting
  • Lead teams through complex, ambiguous challenges in a pharmaceutical/medical device environment
  • Sustaining Engineering Support:
    • Support sustaining engineering programs through risk assessment, design change management, and maintenance of the Design History File and Risk Management File
    • Advice and actively participate in Design Reviews associated with combination products
    • Provide QA and technical support to quality engineers and project teams during ongoing maintenance of the combination product
    • Interact with partners and contract organizations to ensure accurate completion of project milestones, including post-commercialization activities
  • Combination Product Support:
    • Act as Management Representative for the combination products QMS; own policies and procedures
    • Support regulatory inspections and partner audits for combination products
    • Keep the QMS current and inspection-ready via monitoring, gap assessments, and updates
This role requires:
  • BS in Engineering and 8+ years of experience; including combination product or medical device experience; or equivalent combination of education & experience
  • Previous supervisory/ people leadership experience
  • Knowledge of the combination device development and lifecycle process

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Salary Range (annually)

$126,300.00 - $206,100.00

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include:

  • annual bonuses or other incentive plans
  • equity awards
  • pension or retirement benefits
  • 401(k) company match
  • health and wellness programs
  • fitness centers
  • insurance benefits (e.g. medical, dental, vision, life and disability)
  • paid time off
  • family support benefits

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

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