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Medical Device Technical Writer (SOPs)
Medical Device Technical Writer (SOPs)The Fountain Groups • Irving, TX, US
Medical Device Technical Writer (SOPs)

Medical Device Technical Writer (SOPs)

The Fountain Groups • Irving, TX, US
12 hours ago
Job type
  • Part-time
Job description

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.

Base pay range

$50.00 / hr - $57.00 / hr

Direct message the job poster from The Fountain Groups

Senior Engineering Recruiter at The Fountain Group

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

    Seniority level

    Mid-Senior level

    Employment type

    Employment type

    Contract

    Job function

    Job function

    Writing / Editing and Science

    Industries

    Medical Equipment Manufacturing

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