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Biotech Technical Writer Jobs (NOW HIRING)

INCOG

Tech Writer - Tech Services

Fishers, IN

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... 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

PSG Global Solutions

Medical Writer

Chesterfield, MO

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Create drafts of new technical or regulatory documents using existing examples, templates or ...

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

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 ...

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 ...

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 ...

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 ...

LabConnect

Medical Writer

Johnson City, TN · On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

Overview LabConnect improves lives by partnering with pharmaceutical and biotech companies, and ... This role requires strategic thinking with exceptional scientific and technical writing skills ...

Direct Counsel

Patent Agent/Advisor (Biotech)

Palo Alto, CA · On-site

$125K - $205K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Patent Agent/Advisor (Biotech) - Palo Alto Direct Counsel is seeking a Patent Agent/Advisor with a ... Superb technical, written, and verbal communication skills in English. * Initiative-driven, fast ...

Bioclinica

Associate Medical Writer

Princeton, NJ · On-site

We serve more than 400 pharmaceutical, biotechnology, and device organizations The Medical Writer ... Performing other duties as assigned Maintains Technical and Industry Knowledge by: * Staying up-to ...

Synterex

SeniorMedical Writer

Princeton, NJ · On-site +1

Experience (5+ years) as a medical writer in the CRO/biotech/pharmaceutical field * Bachelor's degreeor higherin a relevant field * Oncology, InfectiousDisease, or Vaccineexperiencedesired

BeiGene, Inc.

Associate Director, Medical Writer - Publications

$143K - $193K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Extensive experience collaborating with cross-functional teams and external experts in a biotech or ... Excellent written and verbal communication skills, with a keen eye for scientific accuracy and ...

Synterex

SeniorMedical Writer

NJ · Remote

Experience (5+ years) as a medical writer in the CRO/biotech/pharmaceutical field * Bachelor's degreeor higherin a relevant field * Oncology, InfectiousDisease, or Vaccineexperiencedesired

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Biotech Technical Writer information

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How much do biotech technical writer jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for 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 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 as a biotech technical writer?

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?

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.

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Biotech Technical Writer jobs near you
Infographic showing various Biotech Technical Writer job openings in the United States as of August 2026, with employment types broken down into 60% Full Time, 10% Part Time, and 30% Contract. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Tech Writer - Tech Services

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 15 days ago

Job description

Description
Tech Writer - Tech Services Summary
The Tech Writer will support the TSMS department by creating and maintaining technical documentation for technical transfer and manufacturing activities in accordance with current good manufacturing practices (cGMP) for clinical and commercial programs. This role will work closely with TSMS engineers and cross-functional teams to produce clear, accurate, and compliant documentation that supports manufacturing operations and regulatory requirements.
Essential Job Functions:
  • Develop, author, and maintain technical documents including Process Flow Diagrams, Summary Reports, Process FMEAs, Master Batch Records, Bill of Materials, and Processing Forms under guidance of senior staff
  • Support creation of technical specifications, batch records, forms, and reports ensuring information is clear, detailed, and usable by both technical and non-technical stakeholders
  • Ensure all documentation complies with GMP standards and meets regulatory requirements
  • Collaborate with TSMS engineers, and project teams to gather necessary technical information and ensure documentation reflects current process developments and changes
  • Assist with translating technical data and process monitoring results into comprehensible reports under supervision of senior technical staff
  • Support establishment and maintenance of documentation standards to ensure consistency across technical documents
  • Assist in creating user manuals, training guides, and support materials to aid staff education regarding GMP manufacturing processes and protocols
  • Review and update existing documents to reflect process improvements, new technologies, and regulatory changes
  • Assist with document control activities and maintain accurate records in electronic document management systems (EDMS)
  • Support cross-functional teams by providing clear documentation that facilitates effective communication across departments
  • Participate in document review processes and incorporate feedback from technical subject matter experts
  • Other responsibilities as required

Special Job Requirements:
  • High School diploma required
  • Associate's degree in English, Technical Writing, or scientific/technical discipline preferred
  • 0-2 years of experience 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
  • Basic understanding of GMP manufacturing processes and regulatory requirements preferred
  • Excellent organizational skills with high attention to detail
  • Ability to collaborate effectively with cross-functional teams and communicate complex information to diverse audiences
  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) and familiarity with documentation tools
  • Ability to manage multiple assignments and deadlines with guidance
  • Strong research and information gathering skills

INCOG's Benefits:
• Paid vacation days, amount based on tenure, and paid sick time
• 11 observed holidays
• 401(k) plan with company match up to 3.5% of salary, vested immediately
• Choice of health & wellness plans
• FSA and HSA programs
• Dental & vision care
Additional info about INCOG BioPharma Services:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
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