Technical Document Reviewer – St. Louis, Missouri, United States
Location: United States – St. Louis, Missouri
Category: Quality / Regulatory / Documentation
Job Type: Full-Time
Job Overview
MilliporeSigma is seeking a Technical Document Reviewer to join our St. Louis team. This role is ideal for professionals with a background in life sciences and experience in reviewing technical documentation for medical devices, pharmaceutical, or healthcare products. The Technical Document Reviewer ensures that all in-vitro diagnostic (IVD) product documentation is accurate, compliant with regulatory standards, and aligned with internal quality and style guidelines.
This position plays a critical role in maintaining the integrity and clarity of product manuals, instructions for use, regulatory submissions, risk management files, and other technical documents.
Note: This role does not provide work authorization sponsorship. Applicants must be eligible to work in the U.S.
Key Responsibilities
Review technical documents for IVD products, ensuring compliance with ISO 13485, IVDR, and other applicable regulatory standards.
Assess document clarity, accuracy, consistency, structure, and adherence to internal style guides.
Verify technical content, terminology, formatting, and alignment with product functionality and regulatory requirements.
Maintain version control and ensure up-to-date documents are reviewed and approved.
Provide constructive feedback to authors to enhance document quality, clarity, and compliance.
Collaborate with cross-functional teams to ensure documents accurately reflect product design and regulatory needs.
Support audits as a subject matter expert for documentation processes and quality management systems.
Manage multiple document review projects efficiently in a fast-paced environment.
Qualifications & Experience Required
Minimum Qualifications:
Bachelor’s degree in a scientific discipline (Biology, Chemistry, Microbiology, or related field).
Preferred Qualifications:
1+ years of experience reviewing technical documentation.
Experience in the medical device, healthcare, or pharmaceutical industry.
Knowledge of regulatory requirements for medical device documentation.
Strong analytical, organizational, and time management skills.
Excellent written and verbal communication skills.
Ability to work independently and collaboratively in cross-functional teams.
Compensation & Benefits
Salary Range: $64,400 – $104,900 per year, depending on experience and qualifications.
Eligibility for performance-based bonuses.
Comprehensive benefits package including health insurance, PTO, retirement contributions, and additional employee perks.
Why Join MilliporeSigma?
MilliporeSigma is a global leader in life sciences, healthcare, and laboratory solutions, committed to innovation, quality, and professional development. Our teams collaborate internationally to advance scientific discoveries while maintaining the highest standards of regulatory compliance and quality documentation.
We foster a culture of inclusion, continuous learning, and professional growth, empowering employees to thrive in a global, fast-paced environment.
Application Process
Qualified candidates will be reviewed by our recruitment team, and selected applicants will be contacted with next steps.
Keywords for SEO/GEO/GPT Optimization:
Technical Document Reviewer Jobs, IVD Documentation Specialist, Quality Assurance Documentation, Regulatory Document Review Careers, ISO 13485 Compliance Jobs, Medical Device Documentation Jobs St. Louis, MilliporeSigma Careers, QA Documentation Reviewer, Life Sciences Technical Writer Jobs, IVDR Compliance Specialist.
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