Medical Device Technical Writer; SOPs

1 week ago Be among the first 25 applicants

This range is provided by The Fountain Groups. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$50.00/hr - $57.00/hr

Direct message the job poster from The Fountain Groups

100% ONSITE IRVING TX

PAY: $50-$57/HR

REQUIRED:

• BS Degree preferred/HS Diploma required and 5+ years Technical Writing experience within the medical device/pharma industry writing SOPs.
• 
  Must have med device or pharma experience
  (FDA regulated).
• Preferred bachelors degree in English or communications but GED or High school is all that is required if they have relevant experience.
• Manager wants titled technical writers - job is writing SOP's through and through.

Job Description:

Seeking a detail-oriented and experienced Technical Writer to join our team in the medical device industry. The ideal candidate will be responsible for creating, editing, and maintaining high-quality documentation that supports the development, regulatory compliance and testing of product.

Key Responsibilities:

• Develop and maintain technical documentation including forms, procedures, instructions for testing product, and regulatory documents.
• Translate complex technical information into clear, concise, and user-friendly content for various audiences including technicians and engineers.
• Collaborate with cross-functional teams including R&D, Quality Assurance and Process Owners to gather information and ensure accuracy.
• Ensure all documentation complies with applicable internal policy standards.
• Manage document version control and maintain documentation archives.
• Participate in risk assessments and usability studies to inform documentation strategy.
• Support the creation of training materials and internal SOPs.

Qualifications:

• Bachelor’s degree in English, Communications, Life Sciences, Engineering, or equivalent background and experience in Tech Writing.
• 5+ years of experience in technical writing, preferably in the medical device or healthcare industry.
• Strong understanding of medical terminology and regulatory requirements.
• Proficiency in document management systems and Microsoft Office.
• Familiarity with Good Documentation Practices (GDP) and regulatory processes.
• Excellent written and verbal communication skills.
• Ability to manage multiple projects and meet tight deadlines.

• Seniority level
  
  Mid-Senior level

• Employment type
  
  Contract

• Job function
  
  Writing/Editing and Science
• Industries Medical Equipment Manufacturing

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