Hybrid Regulated Medical Device Technical Writer

Celarity; Minneapolis (MN); Hybrid; USD 52,000 - 62,000; Full time

Job summary

Celarity is seeking a Technical Writer to develop, edit, and maintain high-quality instructions for use, labels, and documentation. The role is contract, with a hybrid location in the Twin Cities Metro, and pay range of $38-$45 per hour.

You will collaborate with engineering, quality, regulatory, and marketing to ensure accuracy, clarity, and regulatory adherence in a medical environment. Responsibilities include creating clinician IFUs, patient manuals, review cycles, revision histories, and

Qualifications

• Bachelor's degree in technical communication, engineering, English, or life sciences.
• 2+ years of technical writing experience in regulated environments.
• Proficiency with Microsoft Office, Adobe Creative Suite, and Content Management Systems.
• Attention to detail and critical thinking skills.
• Experience ensuring regulatory compliance and document control.
• Knowledge of medical terminology and labeling standards.
• Experience with XML-based content management systems (preferred).
• Ability to communicate complex technical information clearly.
• Skilled at cross-functional collaboration and project management.
• Strong problem-solving and risk assessment experience.
• Experience in medical device or healthcare industries.

Responsibilities

• Write and update clinician IFUs, patient manuals, and product labels.
• Review documents with cross-functional teams to ensure accuracy.
• Maintain detailed revision histories and supporting documentation.
• Manage multiple documentation projects simultaneously.
• Ensure all materials meet FDA, ISO, and EU MDR standards.

Skills

Cross-functional collaboration

Project management

Attention to detail

Strong communication

Education

Bachelor's degree in technical communication, engineering, English, or life sciences

Tools

Microsoft Office

Adobe Creative Suite

Content Management Systems

XML CMS

Job description

Celarity is seeking a Technical Writer to develop, edit, and maintain high-quality instructions for use, labels, and documentation. The role is contract, with a hybrid location in the Twin Cities Metro, and pay range of $38-$45 per hour.

You will collaborate with engineering, quality, regulatory, and marketing to ensure accuracy, clarity, and regulatory adherence in a medical environment. Responsibilities include creating clinician IFUs, patient manuals, review cycles, revision histories, and