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Biotech Technical Writer Jobs in Raleigh, NC (NOW HIRING)

Kelly Services

Contract Technical Writer

Raleigh, NC

$40 - $47/hr

... biotech, medical device, or similar manufacturing environment. * Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation. * Working knowledge of CAPA ...

MMS

Senior Nonclinical Writer (US)

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 ...

PSC Biotech

Senior Validation Engineer

Durham, NC

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Strong technical writing and documentation skills. Ability to independently manage complex ...

PSC Biotech

Senior Validation Engineer

Durham, NC · On-site

$120K - $140K/yr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Strong technical writing and documentation skills. * Ability to independently manage complex ...

PSC Biotech

Senior Validation Engineer

Durham, NC · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Strong technical writing and documentation skills. * Ability to independently manage complex ...

Arthur Lawrence

Be Seen First

Manufacturing Technical Operations Specialist

Durham, NC · On-site

$40 - $45/hr

Required Qualifications 3-5 years of experience in pharmaceutical, biotechnology, life sciences, or other regulated manufacturing environments. Strong experience with technical writing and ...

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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 26, 2026, the average hourly pay for biotech technical writer in Raleigh, NC is $37.86, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $45.82 per hour, depending on experience, location, and employer.

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.

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 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 most commonly searched types of Biotech Technical Writer jobs in Raleigh, NC?

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For Biotech Technical Writer jobs in Raleigh, NC, the most frequently searched job titles are:

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Biotech Technical Writer jobs near you
Infographic showing various Biotech Technical Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $78,739 per year, or $37.9 per hour.

(Contract) Quality Technical Writer

Morrisville, NC • Remote

Kymanox
Biotechnology Research and Development • 51 - 200 employees
Learn more about Kymanoxexternal

Contractor

Re-posted 4 days ago

Job description

Job Description:

Is Kymanox the right fit for you?

You want to make a difference and have an impact...

You enjoy having an influence in your day-to-day work...

You are motivated by working alongside a team filled with

subject matter experts who will help you learn and grow...

You wake up every day and do what you do

... because patients deserve better.

If this sounds like you, you've come to the right place.

The Technical Writer - General QMS (Contract)will perform technical writing and client support on a site readiness project authoring a range of engineering, compliance, and commercialization Standard Operating Procedures (SOPs).

Responsibilities:

  • Technical writing may include any of the following focus areas:
    1. Manufacturing equipment and processes
    2. Quality Control Laboratory instruments and methods
    3. Utility systems
    4. Facilities and maintenance equipment
    5. Logistics and warehousing processes
    6. Quality Assurance processes
    7. Environment, Health, and Safety processes
    8. Warehouse and Supply Chain
    9. Information Technology
    10. Training content.

Educational Background:

  • The ideal candidate will have a bachelor's degree in any Engineering discipline (prefer Biomedical, Mechanical, or Chemical engineering) or other STEM discipline (Biology, Chemistry, other) from an accredited institution or equivalent.

Experience:

  • A minimum of 3 to 5 years of experience in development and/or manufacturing in the pharmaceutical, biotechnology, combination product, and/or medical device sectors is required.
  • Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired.

Desired Aptitude and Skill Set:

  • Resourceful
  • Extremely detail oriented
  • Ability to work effectively with remote team members
  • Highly organized
  • Self-directing, self-pacing
  • Excellent written and oral English communication skills
  • Understanding of own limitations
  • Ability to solicit and utilize subject matter expert input
  • Fast learner
  • Pleasant and positive communication style
  • Strong customer-service aptitude
  • Ability to motivate self, team members, and direct reports
  • High energy level
  • Excellent problem-solving skills
  • Seasoned soft skills (i.e., high EQ)
  • Team player

Compensation:

Hourly rate is commensurate with experience, qualifications, and other intangibles evident during the interview process - as well as market conditions.

Travel:

Travel may be necessary to support client work.

About Kymanox:
Join Kymanox - a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries. Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today's biotechnology, pharmaceutical, medical device, and combination product industries. With a reputation of providing unparalleled professional services and our highly collaborative team of engineering, compliance, and project management experts, Kymanox provides an outstanding opportunity for learning and career advancement. Kymanox encourages team members, especially new graduates, and young professionals, to work on a variety of projects to gain increased learnings in Kymanox's service offerings and the life science industry as a whole.

Kymanox is looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market. Kymanox provides professional services related to engineering, compliance, and project management. We service clients ranging from Fortune 100 companies to virtual start-up companies. The company was founded in 2004 and has been growing steadily since its inception. Our corporate HQ is based in Research Triangle Park, NC.

To learn more about our company, please visit our website:Life Science Solutions | Kymanox

Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.

Employment Type: Contractor

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