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Entry Level Biotech Technical Writer Jobs (NOW HIRING)

Evapco

Document Control - Technical Writer I

Greenup, IL · On-site

$53K - $62K/yr

Document Control - Technical Writer I Responsibilities The Document Control - Technical Writer I is ... Experience collaborating with staff at different levels including entry level, plant management to ...

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

Deviation Writer - Tech Services

Fishers, IN · On-site

Minimum of 3 years of experience in technical writing within a regulated GMP environment, preferably in the pharmaceutical, biopharmaceutical, or biotechnology industries. Additional Preferences:

Satori Digital

Biotech Patent Attorney

Carteret, NJ · On-site

Strong legal research, technical writing, and client communication skills * Law firm or IP agency ... Do not have direct experience in biotech or pharmaceutical patent drafting/prosecution * Are ...

Tang Capital

Biotechnology Research Analyst

Manhattan, NY · On-site

$120K - $210K/yr

Position Summary Tang Capital is seeking an entry-level Biotechnology Research Analyst to join its ... technical information, and to translate those insights into clear, concise written deliverables and ...

MMS

Nonclinical Writer

Raleigh, NC · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... This person will participate in the development, writing, and management of highly technical non ...

MMS

Nonclinical Writer

Canton, MI · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... This person will participate in the development, writing, and management of highly technical non ...

MMS

Nonclinical Writer

Boston, MA · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... This person will participate in the development, writing, and management of highly technical non ...

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... This person will participate in the development, writing, and management of highly technical non ...

Tang Capital

Biotechnology Research Analyst

Manhattan, NY · On-site

$120K - $210K/yr

Position Summary Tang Capital is seeking an entry-level Biotechnology Research Analyst to join its ... technical information, and to translate those insights into clear, concise written deliverables and ...

Apogee Enterprises, Inc.

Factory Order Writer

Monett, MO · On-site

Position Summary Entry level position to lead into FO Technician II and other roles in Engineering ... Communicate effectively in a verbal and a written manner, and the ability to identify an issue and ...

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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 Jul 13, 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 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.

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.
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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 July 2026, with employment types broken down into 19% Locum Tenens, 76% Full Time, 1% Part Time, and 4% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.
Document Control - Technical Writer I

Document Control - Technical Writer I

Evapco

Greenup, IL • On-site

$53K - $62K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

EVAPCO rating

8.5

Company rating: 8.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

66th of 430 rated machine equipment manufacturers

Job description

Document Control - Technical Writer I
Responsibilities
The Document Control - Technical Writer I is responsible for creation, review, control, distribution, and timeliness of documents that will be used by Evapco employees. Material includes policies, procedures, guidelines, forms, templates, and other training material. While providing outstanding training services and a high degree of employee care to issues of documentation and instruction for the Evapco Greenup Facility.
Job Summary
Work with limited direct supervision, prioritizing work, making sound decisions of timing, training, and responsibility. Training and development of all Levels Evapco personnel with approved and certified corporate and internal documents and training techniques. Ensuring training documentation, and processes are accurate and maintain their quality, and present information for greatest reader comprehension based on the audiences' needs.
Knowledge, Skills, & Experience
  • High School Diploma or GED Equivalent is required. Preferred applicants will have an Associate Degree or Bachelor's Degree or equivalent work experience.
  • Strong written and verbal communication and experience working with content in SharePoint and other programs.
  • Experience with Microsoft Office Suite and Internet and ability to troubleshoot issues.
  • Proficiency working with Subject Matter Experts to create documentation or other training material.
  • Ability to understand and adhere to quality documentation standards and Document Control processes and procedures.
  • Experience collaborating with staff at different levels including entry level, plant management to Corporate Document Control Specialist.
  • Strong organizational skills and the ability to meet deadlines, prioritize, and work on multiple projects simultaneously with great efficiency and attention to detail.
  • Must be a self-starter with the ability to work in an atmosphere with high standards for quality, accuracy, and innovation.
  • Knowledge and practical use of mfg. tools, test equipment, and measurement equipment is preferred.
  • Experience in interviewing subject matter experts, documenting technical information and creating training material for effective use at all levels of operations.

Essential Functions
  • Ability to interview subject matter experts, document technical information and create training material (documents, job aids, video etc.) for effective use at all levels of operations.
  • Guarantee documents are created, signed off, data is accurate, and documents are stored and backed up and any retention policies are followed; while ensuring product requirements and Evapco Procedures concerning process instructions, build techniques, and acceptable product.
  • Meet Document Control production expectations within 3 months of start date and maintain production expectations throughout duration of role.
  • Facilitate New Hire Training covering SharePoint, Pilot, and ADP.
  • Monitoring training completion for employees and assisting employees with training completion as needed.
  • Continually gather customer feedback on training material to improve usability. Act as editor to ensure consistency in material across all departments and plants.
  • Develop revisions of work instruction and standards to meet new/existing product or equipment mixes.
  • Review documentation with applicable individuals on-site and providing that information to corporate.
  • Contribute "new ideas" for training improvements and system improvements within the organization.
  • Completion of projects such as: Video presentation of training events, safety procedures, and Leader / Assistant leader Document Review Sign Offs.
  • Use of Microsoft Office Suite, Scanning, Electronic files, and SharePoint daily.
  • Work with Subject Matter Experts to collect, document, record, and maintain all pertinent data required to successfully complete assigned work and be able to report back to supervisor of status.
  • Follows documented Office, Safety, and Quality policies, follows standard processes, and ensures projects are completed on time and meet quality standards.
  • Required to maintain a professional and positive demeanor when working with other Evapco Team Members, Representatives, and Customers.

Pay & Benefits:
• The salary range consists of base pay and most recent profit sharing bonus amounts
• Medical, Vision, & Dental Insurance
• Employee Stock Ownership Program - we are an employee-owned company
• Profit Sharing Bonus - which is paid twice per year
• (k)larity Plan - Voluntary Employee Retirement Savings Plan
• Paid Holidays
• Paid Vacation
• Paid Maternity and Paternity Leave
• Bereavement Pay
• Company Paid Basic Life Insurance equivalent to base salary, with option for Supplemental Life election
• Paid Sick Leave
• Long Term Disability
Pay Range: $53,000 - $62,000 per year

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