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Biotech Technical Writer Jobs in Ohio (NOW HIRING)

PSC Biotech

CQV Engineer

Columbus, OH · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Strong technical writing skills and understanding of full lifecycle documentation (protocols ...

PSC Biotech

Validation Engineer

Columbus, OH

PSC Biotech provides the life sciences with essential services to ensure that health care products ... technical troubleshooting and analytical skills. Excellent written and verbal communication skills ...

PSC Biotech

Validation Engineer

Columbus, OH

$100K - $160K/yr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Strong technical troubleshooting and analytical skills. * Excellent written and verbal ...

PSC Biotech

Validation Engineer

Columbus, OH · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Strong technical troubleshooting and analytical skills. * Excellent written and verbal ...

Ultimate Solutions

C&Q Engineer, Sr.

Columbus, OH · On-site

$100K - $138K/yr

Experience with automation systems, process equipment, and utilities in pharmaceutical or biotechnology manufacturing. * Excellent technical writing, analytical, and organizational skills. * Strong ...

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Biotech Technical Writer information

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$13

$37

$62

How much do biotech technical writer jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for biotech technical writer in Ohio is $37.02, according to ZipRecruiter salary data. Most workers in this role earn between $27.40 and $44.81 per hour, depending on experience, location, and employer.

What are the common challenges faced by Biotech Technical Writers in their daily work?

Biotech Technical Writers often encounter the challenge of translating highly technical and complex scientific data into clear, concise documents for diverse audiences, including regulatory agencies and non-specialist stakeholders. They must stay up-to-date with evolving regulations and industry best practices, which can be demanding in a rapidly changing biotech landscape. Additionally, working closely with subject matter experts from research, development, and regulatory teams requires strong collaboration and communication skills to ensure accuracy and consistency. Overcoming these challenges not only sharpens your abilities but also makes you an invaluable asset within interdisciplinary biotech environments.

What are the key skills and qualifications needed to thrive in the Biotech Technical Writer position, and why are they important?

To thrive as a Biotech Technical Writer, you need a solid understanding of scientific concepts, excellent written communication skills, and often a degree in life sciences, biotechnology, or a related field. Familiarity with document management systems, scientific publishing software, and regulatory compliance guidelines such as Good Laboratory Practices (GLP) or FDA requirements is typically required. Strong attention to detail, adaptability, and the ability to collaborate with cross-functional teams are essential soft skills in this position. These competencies are crucial for effectively translating complex scientific content into clear, accurate documentation that supports research, product development, and regulatory submissions.

What is a Biotech Technical Writer job?

A Biotech Technical Writer creates clear, accurate, and concise documentation related to biotechnology, such as research reports, regulatory submissions, standard operating procedures (SOPs), and product manuals. They translate complex scientific concepts into understandable content for various audiences, including researchers, regulators, and the general public. This role requires strong writing skills, attention to detail, and knowledge of biotech terminology and industry regulations. Biotech Technical Writers often collaborate with scientists, engineers, and regulatory professionals to ensure documentation meets industry standards.

What are the most commonly searched types of Biotech Technical Writer jobs in Ohio? The most popular types of Biotech Technical Writer jobs in Ohio are:
What are popular job titles related to Biotech Technical Writer jobs in Ohio? For Biotech Technical Writer jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Biotech Technical Writer jobs in Ohio look for? The top searched job categories for Biotech Technical Writer jobs in Ohio are:
Biotech Technical Writer jobs near you
Infographic showing various Biotech Technical Writer job openings in Ohio as of July 2026, with employment types broken down into 2% As Needed, 86% Full Time, 5% Part Time, 1% Temporary, and 6% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $77,007 per year, or $37 per hour.

Scientific Technical Writer

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Other

Medical, Retirement, PTO

Re-posted 20 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

14th of 72 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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