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Entry Level Medical Device Technical Writer Jobs

The Contingent Plan

Technical Writer II

San Diego, CA · On-site

Pharmaceutical and/or medical device experience preferred. * Understanding of cGMP, ISO13485, and regulatory requirements * Three years of experience working as a technical writer. * Project ...

Three Point Solutions

Medical Assembler

Dexter, MI · On-site

$20 - $22/hr

Ability to read and follow written and verbal instructions. * Legible handwriting and documentation ... Medical device manufacturing experience. * Cleanroom manufacturing experience. * Technical ...

Three Point Solutions, Inc.

Medical Assembler

Dexter, MI · On-site

$17.25 - $21/hr

Ability to read and follow written and verbal instructions. * Legible handwriting and documentation ... Medical device manufacturing experience. * Cleanroom manufacturing experience. * Technical ...

Three Point Solutions

Medical Assembler

Dexter, MI · On-site

$20 - $22/hr

Ability to read and follow written and verbal instructions. * Legible handwriting and documentation ... Medical device manufacturing experience. * Cleanroom manufacturing experience. * Technical ...

Three Point Solutions, Inc.

Medical Assembler

Dexter, MI · On-site

$17.25 - $21/hr

Ability to read and follow written and verbal instructions. * Legible handwriting and documentation ... Medical device manufacturing experience. * Cleanroom manufacturing experience. * Technical ...

MagVenture

Be Seen First

Medical Device Customer Support Technician

Alpharetta, GA · On-site

$55K - $64K/yr

We are seeking an entry-level Medical Device Customer Support Technician to serve as the first ... Provide technical support and service on medical devices , addressing all incoming requests via ...

Analygence

Technical Writer

Fort George G Meade, MD

This entry-level role is designed to provide hands-on experience and rapid skill development in technical writing, document control, research methodologies, formatting standards, and style guide ...

Analygence

Technical Writer

Fort George G Meade, MD · On-site

This entry-level role is designed to provide hands-on experience and rapid skill development in technical writing, document control, research methodologies, formatting standards, and style guide ...

The LaSalle Group

Technical Writer

Chicago, IL · On-site

$30 - $40/hr

... entry-level positions to the C-suite. With units specializing in Accounting and Finance ... Family Medical Leave, Worker's Compensation, Paid Leave and Sick Leave are also provided. View a ...

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Entry Level Medical Device Technical Writer information

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$14

$38

$57

How much do entry level medical device technical writer jobs pay per hour?

As of Jul 12, 2026, the average hourly pay for entry level medical device technical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Medical Device Technical Writer vs Medical Device Quality Assurance Associate?

AspectEntry Level Medical Device Technical WriterMedical Device Quality Assurance Associate
Required CredentialsBachelor's in Life Sciences, Writing or related field; certifications like RAPS or regulatory writing helpfulBachelor's in Engineering, Life Sciences, or related; certifications like ISO or GMP training beneficial
Work EnvironmentOffice setting, documentation teams, regulatory departmentsManufacturing facilities, quality labs, compliance departments
Employer & Industry UsageMedical device companies, regulatory agencies, consulting firmsManufacturers, medical device firms, healthcare companies
Common Search & ComparisonYesYes

While both roles support the medical device industry, Entry Level Medical Device Technical Writers focus on creating and managing technical documentation, whereas Medical Device Quality Assurance Associates ensure product compliance and quality standards. Both positions require relevant certifications and work within similar industry environments, but their core responsibilities differ significantly.

More about Entry Level Medical Device Technical Writer jobs
What are the most commonly searched types of Medical Device Technical Writer jobs? The most popular types of Medical Device Technical Writer jobs are:
What states have the most Entry Level Medical Device Technical Writer jobs? States with the most job openings for Entry Level Medical Device Technical Writer jobs include:
What job categories do people searching Entry Level Medical Device Technical Writer jobs look for? The top searched job categories for Entry Level Medical Device Technical Writer jobs are:
Entry Level Medical Device Technical Writer jobs near you
Infographic showing various Entry Level Medical Device Technical Writer job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, 18% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Medical Device Complaint Specialist

Medical Device Complaint Specialist

Three Point Solutions, Inc.

Moundsview, MN • On-site

Full-time

Re-posted 22 days ago

Job description

Job Title: Medical Device Complaint Specialist
Client: Medical Device Manufacturing Company
Location: Mounds View, MN 55112
Duration: 12 Months (Possible Extension)
Shift: 1st Shift
Job Summary
Entry-level medical device safety and complaint investigation role responsible for intake, documentation, adverse event reporting, MDR submissions, and vigilance activities for Neurovascular products while ensuring compliance with regulatory requirements.
Key Responsibilities
• Review, document, and investigate product complaints
• Process Medical Device Reports (MDRs) and adverse event cases
• Maintain accurate complaint and vigilance records
• Analyze safety and clinical data for reporting purposes
• Ensure compliance with FDA and global regulatory requirements
• Support complaint investigations and follow-up activities
• Collaborate with cross-functional teams and external partners
• Assist with process improvements and quality initiatives
• Prepare regulatory documentation and reports
Core Duties
• Complaint handling & investigation
• Medical Device Reporting (MDR)
• Adverse event processing
• Regulatory compliance support
• Safety data review & analysis
• Documentation & case management
Required Skills
• Critical thinking and decision-making
• Strong attention to detail
• Excellent written and verbal communication
• Investigation and problem-solving skills
• Documentation and record management
• Organization and time management
Preferred Skills
• Medical device industry experience
• Pharmaceutical industry experience
• Complaint handling experience
• Regulatory reporting knowledge
• Quality or compliance exposure
• Clinical data review experience
Technical / Functional Exposure
• Medical Device Reporting (MDR)
• Vigilance & Post-Market Surveillance
• Complaint Investigation
• Adverse Event Reporting (ADE)
• Regulatory Compliance
• Clinical & Safety Data Analysis
Work Environment
• Medical device regulatory and quality environment
• Cross-functional collaboration with quality, regulatory, and clinical teams
• Process-driven and compliance-focused role
• Training and development opportunities for entry-level professionals
Education / Experience
• Bachelor's Degree in Bio-Sciences, Engineering, Life Sciences, or related field required
• Experience in Medical Device, Pharmaceutical, Quality, Regulatory, Clinical, or related industry
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