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Pharmaceutical Technical Writer Jobs in Raleigh, NC

Kelly Services

Contract Technical Writer

Raleigh, NC

$40 - $47/hr

... regulated pharmaceutical, biotech, medical device, or similar manufacturing environment ... Strong technical writing skills with an emphasis on clarity, consistency, and regulatory compliance.

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 ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · Remote

Experience leading regulatory submission projects, including Common Technical Document (CTD ... Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions, Scientific Writing ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site

Experience leading regulatory submission projects, including Common Technical Document (CTD ... Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions, Scientific Writing ...

GSK

Principal Medical Writer

Durham, NC · On-site

Experience leading regulatory submission projects, including Common Technical Document (CTD ... Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions, Scientific Writing ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · Remote

Experience leading regulatory submission projects, including Common Technical Document (CTD ... Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions, Scientific Writing ...

Visium Resources, Inc.

Be Seen First

Pharmaceutical Engineer

Raleigh, NC · On-site

$120K - $145K/yr

Lead and execute CQV activities for pharmaceutical and biotech capital projects. * Develop and ... Strong technical writing and documentation skills. * Ability to work independently within fast ...

ALL4 LLC

Technical Consultant

Morrisville, NC

... and technical writing ability. * Commitment to excellence and ALL4's core values; openness to ... chemical/pharmaceutical, waste management, power, oil and gas, and automotive. ALL4 has been ...

ALL4 All

Technical Consultant

Morrisville, NC · On-site

... and technical writing ability. * Commitment to excellence and ALL4's core values; openness to ... chemical/pharmaceutical, waste management, power, oil and gas, and automotive. ALL4 has been ...

ALL4 LLC

Technical Consultant

Morrisville, NC · On-site

... and technical writing ability. * Commitment to excellence and ALL4's core values; openness to ... chemical/pharmaceutical, waste management, power, oil and gas, and automotive. ALL4 has been ...

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All JobsPharmaceutical Technical Writer JobsPharmaceutical Technical Writer Jobs in Raleigh, NC

Pharmaceutical Technical Writer information

See Raleigh, NC salary details

$13

$37

$64

How much do pharmaceutical technical writer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for pharmaceutical technical writer in Raleigh, NC is $37.85, 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.

How does a pharmaceutical technical writer collaborate with scientists and regulatory teams during document preparation?

Pharmaceutical Technical Writers work closely with scientists, researchers, and regulatory affairs teams to ensure that all documentation—such as clinical study reports, regulatory submissions, and standard operating procedures—is accurate, clear, and compliant with industry standards. Collaboration often involves attending meetings to discuss project requirements, clarifying scientific data with subject matter experts, and incorporating feedback from multiple stakeholders. This cross-functional teamwork is essential for producing high-quality documents that meet both scientific rigor and regulatory expectations.

What is the difference between Pharmaceutical Technical Writer vs Pharmaceutical Regulatory Affairs Specialist?

AspectPharmaceutical Technical WriterPharmaceutical Regulatory Affairs Specialist
CredentialsBachelor's in life sciences or related field; writing certifications helpfulBachelor's in life sciences, law, or related; regulatory certifications preferred
Work EnvironmentPharmaceutical companies, CROs, biotech firmsRegulatory agencies, pharmaceutical companies, consulting firms
Industry UsageCreating SOPs, clinical trial documents, product labelsPreparing submissions, ensuring compliance, liaising with authorities
Search/Comparison IntentUnderstanding roles, career paths, required skillsRegulatory processes, compliance, documentation requirements

The Pharmaceutical Technical Writer focuses on creating clear, accurate documentation such as SOPs and clinical reports, while the Pharmaceutical Regulatory Affairs Specialist handles regulatory submissions and compliance. Both roles require strong knowledge of pharmaceutical processes, but their primary responsibilities and work environments differ.

What skills and qualifications are needed to be a pharmaceutical technical writer?

To thrive as a Pharmaceutical Technical Writer, a background in life sciences, strong writing skills, and knowledge of regulatory requirements are essential, often supported by a relevant degree. Familiarity with document management systems, regulatory submission tools, and industry-specific style guides like ICH or EMA guidelines is typically required. Attention to detail, ability to synthesize complex information, and strong collaboration skills help individuals excel in this role. These skills ensure accuracy, compliance, and clarity in documentation critical for regulatory approval and safe pharmaceutical development.

What does a pharmaceutical technical writer do?

A Pharmaceutical Technical Writer creates clear, accurate, and compliant documentation related to pharmaceutical products and processes. This includes writing and editing regulatory submissions, standard operating procedures (SOPs), clinical study reports, manufacturing instructions, and other technical documents. Their work ensures that complex scientific information is communicated effectively to regulatory authorities, healthcare professionals, and internal stakeholders. They must have a strong understanding of scientific concepts, regulatory guidelines, and industry standards to produce high-quality documentation.
What are popular job titles related to Pharmaceutical Technical Writer jobs in Raleigh, NC? For Pharmaceutical Technical Writer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Technical Writer jobs in Raleigh, NC look for? The top searched job categories for Pharmaceutical Technical Writer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Pharmaceutical Technical Writer jobs? Cities near Raleigh, NC with the most Pharmaceutical Technical Writer job openings:
Pharmaceutical Technical Writer jobs near you
Infographic showing various Pharmaceutical Technical Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 69% Full Time, and 31% Contract. Highlights an 100% In-person job distribution, with an average salary of $78,735 per year, or $37.9 per hour.

(Contract) Quality Technical Writer

Kymanox

Morrisville, NC • On-site

Contractor

Posted 19 days ago

Job description

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.

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