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Medical Writing Quality Control Reviewer Jobs (NOW HIRING)

Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize ... writing. Quality Control * Ensure that all work is complete and of high quality prior to team ...

Revolution Medicines is seeking a motivated individual with a clinical regulatory writing ... Experience performing QC reviews of clinical regulatory documents. #LI-Hybrid #LI-JC1

Eldridge Writing invites you to apply for our Medical Writing Apprenticeship Position! About Us ... We pride ourselves on unwavering quality, dependable execution, trusted judgment, and exceptional ...

New

Perform peer QC review asneeded * Contribute to medical writing operational initiatives (e.g., templates, style guides, reference management), if needed Requirements * Experience (5+ years) as a ...

Principal Medical Writer

$152K - $190K/yr

Help establish and refine medical writing processes, templates, and standards to ensure consistency, quality, and accuracy across all deliverables. Implement and manage efficient document workflows ...

Perform independent quality reviews of training analyses, evaluation plans, technical reports ... Coordinate with the ISD III Lead, instructional analysts, SMEs, technical writers, and the Program ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Medical Writing Manager

Fresno, CA · Remote

$50 - $80/hr

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

Your work will shape how models learn, reason, and perform through high-quality, real-world input ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...

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Medical Writing Quality Control Reviewer information

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How much do medical writing quality control reviewer jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for medical writing quality control reviewer in the United States is $42.06, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $54.09 per hour, depending on experience, location, and employer.

What does a medical writing quality control reviewer do?

A Medical Writing Quality Control Reviewer is responsible for ensuring the accuracy, clarity, consistency, and compliance of medical documents such as clinical study reports, regulatory submissions, and manuscripts. They meticulously review documents for grammar, style, formatting, and data integrity, often using checklists and standardized procedures. Their work helps ensure that medical documents meet regulatory requirements and company standards before submission or publication, ultimately supporting patient safety and scientific integrity.

What are the key skills and qualifications needed to thrive as a medical writing quality control reviewer?

To thrive as a Medical Writing Quality Control Reviewer, you need a strong background in life sciences, attention to detail, and experience with regulatory or scientific writing standards, often supported by a relevant degree. Familiarity with style guides (e.g., AMA, ICH), document management systems, and QC tools like track changes or proofreading software is essential. Excellent communication, critical thinking, and organizational skills set top performers apart. These skills ensure the accuracy, compliance, and clarity of medical documents, which are vital for regulatory submissions and scientific integrity.

What are some common challenges medical writing quality control reviewers face when ensuring document accuracy?

Medical Writing Quality Control Reviewers often encounter challenges such as managing tight deadlines while thoroughly checking for consistency, accuracy, and compliance with regulatory standards. They must stay updated on evolving guidelines and terminology, and frequently collaborate with medical writers, subject matter experts, and regulatory teams to resolve discrepancies. Balancing attention to detail with efficiency is crucial, as even minor errors can have significant regulatory or scientific implications. Effective communication and a systematic approach help reviewers maintain high-quality standards across various documents.

What are popular job titles related to Medical Writing Quality Control Reviewer jobs?

For Medical Writing Quality Control Reviewer jobs, the most frequently searched job titles are:

Infographic showing various Medical Writing Quality Control Reviewer 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 $87,476 per year, or $42.1 per hour.

FSP - QC Reviewer

Foster City, CA • On-site

Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

$67K - $80K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 19 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 432 frontline employees who took The Breakroom Quiz


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

QC REVIEWER:

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

This role is based onsite in: Foster City, CA

Key responsibilities:

  • Review raw data
  • Numerical data verification for regulatory filings
  • Transcribe SOPs
  • Perform administrative updates
  • Consolidate data for QC metrics
  • Author clinical and commercial stability protocols
  • Evaluates laboratory data for compliance with analytical methods and SOPs.
  • Reviews sample results for completeness and accurate representation of the data and report findings.
  • Communicates with laboratory staff to proactively address the quality of laboratory documentation.
  • Prepares QC statements noting deficiencies with the analytical data set or notebooks. Reports deficiencies to the project leader for correction.
  • Trains new QC Reviewers and laboratory staff.
  • Conducts SOP review and writing. Conducts consultations for quality records.
  • Performs other duties as assigned.

Education and Experience:

  • Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar
  • 2+ years of previous experience that provides the knowledge, skills, and abilities to perform the job OR Masters degree

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

  • Thorough knowledge of SOPs and Federal Regulations to include GLP and GMP
  • Thorough knowledge of chromatography and divisional SOPs
  • Strong technical knowledge including an understanding of laboratory procedures, methodology and standards
  • Strong verbal and written communication skills
  • Strong attention to detail
  • Ability to train staff
  • Ability to independently review laboratory reports and analytical methods
  • Ability to deal with multiple and changing priorities
  • Ability to provide clear and concise feedback and/or documentation of results
  • Ability to work in a collaborative team environment

Working Environment:

  • Below is listed the working environment/requirements for this role:
  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
  • Able to work upright and stationary and/or standing for typical working hours.
  • Able to lift and move objects up to 25 pounds
  • Able to work in non-traditional work environments.
  • Able to use and learn standard office equipment and technology with
  • proficiency.
  • May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Compensation and Benefits

The salary range estimated for this position based in California is $67,699.00–$80,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards


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