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Technical Writer II

Insight Global

Arden Hills, MNJobSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Arden Hills, MN
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Insight Global seeks a Technical Writer II for a medical device manufacturer to develop, edit, and maintain high‑quality Instructions for Use, patient manuals, and labels, ensuring regulatory compliance and clear, user‑focused content through collaboration with cross‑functional teams.

Skills & qualifications

RequiredNice to have

Skills

Microsoft Office SuiteAdobe Creative SuiteContent Management SystemsQuality Management SystemsXML Based Content Management SystemWritingTechnical WritingAttention to DetailCritical ThinkingProblem SolvingMedical TerminologyAnatomy

Qualifications

Bachelor's Degree in Technical Communication, English, Biomedical Engineering or a Life Science DisciplineMinimum 2+ Years Technical Writing ExperienceAdvanced Degree in Technical Communications, English or Similar

Full job description

Job Description

Insight Global is looking for a Technical Writer II to join a leading medical device manufacturing company to be responsible for developing, editing, and maintaining high-quality Instructions for Use (IFUs) and labels that support clinician use, patient safety, and regulatory compliance. The ideal candidate is detail-oriented, collaborative, and skilled at translating complex technical information into clear, user-focused content. Responsibilities

  • Writing: Exceptional writing and communication skills.
  • Document Authoring: Create and update clinician IFUs, patient manuals, and product labels.
  • Cross-Functional Collaboration: Lead documentation reviews with engineering, quality, clinical, regulatory, marketing, and manufacturing teams to ensure technical accuracy and regulatory compliance.
  • Regulatory Compliance: Ensure all materials conform to strict standards including FDA guidelines, ISO norms, and EU MDR requirements.
  • Document Control: Create and maintain precise revision histories and supporting documentation for risk management.
  • Project Management: Create and adhere to project plans for document completion. Manage multiple projects simultaneously as required.

Skills and Requirements

  • Education: Bachelor's degree in Technical Communication, English, Biomedical Engineering, or a Life Science discipline.
  • Experience: Minimum of 2+ years of technical writing experience within a regulated, medical, or manufacturing environment.
  • Technical Proficiency: Mastery of tools like Microsoft Office Suite, Adobe Creative Suite, and experience using Content Management and Quality Management Systems.
  • Advanced degree in technical communications, English or similar
  • Document creation using an XML-based content management system
  • Writing for multiple audiences (clinicians and patients)
  • Strong attention to detail
  • Knowledge of medical terminology and anatomy
  • Proven understanding of literature and labeling development in a heavily-regulated environment
  • Use of critical-thinking and problem-solving skills to identify risk and develop creative solutions

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].

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