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Entry Level Biotech Technical Writer Jobs (NOW HIRING)

Markon

Junior Technical Writer

Annapolis Junction, MD · On-site

$80K - $95K/yr

Description PLEX Solutions, A Part of Markon, is looking for an Entry Level Technical Writer to join a fast-paced program in the Annapolis Junction, MD area. This is a customer facing role and ...

Markon

Junior Technical Writer

Annapolis Junction, MD · On-site

$80K - $95K/yr

PLEX Solutions, A Part of Markon, is looking for an Entry Level Technical Writer to join a fast-paced program in the Annapolis Junction, MD area. This is a customer facing role and requires a ...

Markon

Junior Technical Writer

Annapolis Junction, MD · On-site

$80K - $95K/yr

Description PLEX Solutions, A Part of Markon, is looking for an Entry Level Technical Writer to join a fast-paced program in the Annapolis Junction, MD area. This is a customer facing role and ...

Aequor

Experience working in GMP pharma and/or biotechnology industry. Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing. Experience with device ...

Merck & Co.

Specialist Technical Writing

New Albany, OH · On-site

$70 - $100/hr

Experience working in GMP pharma and/or biotechnology industry. * Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing. * Experience with ...

Tjoapack

Validation Writer

Clinton, TN · On-site

Your primary responsibility is entry level Technical Writing- authoring product-specific Master Batch Records (MBRs) executed during production, as well as equipment and component specific validation ...

Tjoapack

Validation Writer

Clinton, TN · On-site

Your primary responsibility is entry level Technical Writing- authoring product-specific Master Batch Records (MBRs) executed during production, as well as equipment and component specific validation ...

INCOG

Tech Writer - Tech Services

Fishers, IN

... in technical writing, preferably in a GMP environment or pharmaceutical/biotechnology industry * Strong writing skills with ability to create clear, concise, and accurate technical documentation

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Entry Level Biotech Technical Writer information

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

As of Aug 23, 2026, the average hourly pay for entry level biotech technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What does an entry level biotech technical writer do?

An Entry Level Biotech Technical Writer is responsible for creating clear and accurate documentation related to biotechnology products, processes, and research. They work closely with scientists, engineers, and regulatory experts to translate complex technical information into user manuals, standard operating procedures, and regulatory submissions. This role often involves editing and organizing scientific data, ensuring compliance with industry standards, and helping non-experts understand technical concepts. Strong writing skills, attention to detail, and the ability to learn technical subjects quickly are key requirements for success in this position.

What are the key skills and qualifications needed to thrive as an entry level biotech technical writer, and why are they important?

To thrive as an Entry Level Biotech Technical Writer, you need a solid foundation in biological sciences or a related field, along with strong written communication skills and attention to detail. Familiarity with document management systems, Microsoft Office Suite, and sometimes regulatory guidelines like FDA or GxP is typically required. Outstanding organization, adaptability, and the ability to translate complex scientific concepts for diverse audiences help set candidates apart. These skills ensure the accurate, clear, and compliant documentation essential for regulatory submissions and scientific communication in the biotech industry.

What are some common challenges faced by entry level biotech technical writers, and how can they be addressed?

Entry-level biotech technical writers often encounter the challenge of translating complex scientific information into clear, accessible documents for diverse audiences. Navigating unfamiliar technical jargon and rapidly learning new concepts can be daunting, especially when working with experienced scientists or engineers. To address these challenges, it's helpful to proactively ask clarifying questions, seek mentorship from senior writers, and leverage style guides or templates commonly used in the organization. Regular collaboration with subject matter experts also builds confidence and improves the accuracy of documentation while fostering valuable professional relationships.

What is the difference between Entry Level Biotech Technical Writer vs Entry Level Scientific Writer?

AspectEntry Level Biotech Technical WriterEntry Level Scientific Writer
CredentialsBachelor's in Life Sciences, Biology, or related field; strong writing skillsBachelor's in Science, Biology, Chemistry, or related; good writing and research skills
Work EnvironmentBiotech companies, pharmaceutical firms, research labsAcademic institutions, research organizations, biotech firms
Employer UsageCreating technical documentation, regulatory submissions, user manualsWriting research articles, grant proposals, scientific reports

Entry Level Biotech Technical Writers focus on creating technical documents for biotech and pharma industries, often involving regulatory and compliance content. Entry Level Scientific Writers typically produce research-based content like articles and reports. While both roles require strong scientific knowledge and writing skills, their work environments and document types differ, making them distinct career paths within the scientific communication field.

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Entry Level Biotech Technical Writer jobs near you
Infographic showing various Entry Level Biotech Technical Writer job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Scientific Technical Writer

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, Retirement, PTO

Re-posted 12 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 74 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.

What Medpace employees say

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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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