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Remote Medical Device Technical Writer Jobs in Ohio

Cardinal Health

... medical device companies worldwide. We support clients throughout the full product lifecycle ... Excellent interpersonal skills. #LI-Remote Candidates who are back-to-work, people with ...

Cardinal Health

... medical device companies worldwide. We support clients throughout the full product lifecycle ... Proficiency in document management tools (e.g., Veeva, MS Office) #LI-Remote Candidates who are ...

Medpace, Inc.

Clinical Data Coder

Cincinnati, OH · On-site +1

$18 - $22.75/hr

... medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country ...

Sotera Health

Sr. Manager Tax

Broadview Heights, OH · Remote

... 50 medical device companies and 9 of the top 10 pharmaceutical companies. Senior Manager, Tax We ... S. corporate income tax, with strong technical knowledge of ASC 740, Accounting for Income Taxes, U.

Alleima

This is a remote position with approximately 50%travelrequired. Yourhunter focusedrole will involve ... experience in medical device sales, OEM relationships, or technical consultative selling. Your ...

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Remote Medical Device Technical Writer information

What is the difference between Remote Medical Device Technical Writer vs Remote Regulatory Affairs Specialist?

AspectRemote Medical Device Technical WriterRemote Regulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences, engineering, or related field; certifications like RMT or technical writing certifications are commonRequires degrees in life sciences, law, or regulatory fields; certifications like RAC are often preferred
Work EnvironmentPrimarily writes and edits technical documents remotely for medical device companiesFocuses on regulatory submissions, compliance, and communication with authorities, often remotely
Industry UsageUsed across medical device companies, biotech, and healthcare tech firmsCommon in medical device, pharmaceutical, and biotech industries

While both roles require knowledge of medical devices and regulatory standards, the Remote Medical Device Technical Writer primarily creates technical documentation, whereas the Remote Regulatory Affairs Specialist manages regulatory compliance and submissions. Both roles often work remotely and require relevant industry experience, but their core responsibilities differ significantly.

What are the most commonly searched types of Medical Device Technical Writer jobs in Ohio?

The most popular types of Medical Device Technical Writer jobs in Ohio are:

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For Remote Medical Device Technical Writer jobs in Ohio, the most frequently searched job titles are:

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The top searched job categories for Remote Medical Device Technical Writer jobs in Ohio are:

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Cities in Ohio with the most Remote Medical Device Technical Writer job openings:

Remote Medical Device Technical Writer jobs near you

Scientific Technical Writer

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 6 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research

Job description

Job Summary

Our bioanalytical services are growing rapidly, and we are currently seeking a full-time, office based Scientfic Technical Writer to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Assist Scientists to prepare protocols, methods and reports for sponsors' studies;
  • Organize study documents, such as, notebooks, sample receiving documents, CoAs of reference standards, etc., for individual studies;
  • Compile and review all results from instruments and Watson-LIMS database for report writing;
  • Able to use templates to prepare protocols and reports for scientists in an efficient manner.
Qualifications
  • A minimum of a Bachelor's degree, with previous experience in a research laboratory;
  • Writing communication prefered;
  • Knowledge of GLP, cGMP, and ICH guidelines;
  • Strong organizational and communication (written and oral) skills; and
  • Knowledge of Microsoft Word, Excel, and Powerpoint.

Travel: None

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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