Medical Device Technical Writer (SOPs)

The Fountain Groups

Irving (TX)

On-site

USD 104,000 - 118,000

Full time

14 days+

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Job summary

A leading company in the medical device industry is seeking a Senior Engineering Recruiter to create and maintain technical documentation. The role requires strong technical writing skills and experience in a regulated environment. The ideal candidate will work onsite in Irving, TX and engage with various teams to ensure compliance and quality documentation.

Qualifications

5+ years of experience in technical writing, preferably in the medical device or healthcare industry.
Strong understanding of medical terminology and regulatory requirements.
Excellent written and verbal communication skills.

Responsibilities

Develop and maintain technical documentation including forms, procedures, and regulatory documents.
Translate complex technical information into clear, concise content for various audiences.
Collaborate with cross-functional teams for accuracy.

Skills

Technical Writing

Regulatory Compliance

Communication

Document Management

Education

Bachelor’s degree in English, Communications, Life Sciences, Engineering

HS Diploma

Tools

Microsoft Office

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