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

Novartis

Process Engineer III

Durham, NC · On-site

$98K - $183K/yr

Excellent written and verbal communication skills with strong technical writing capabilities ... biotechnology environment * Proven ability to lead cross-functional teams in a fast-paced and ...

Astrix Inc

Manufacturing Associate

Holly Springs, NC · On-site

As a guiding force in the biotech industry, they set the bar for innovation and advancement. We are ... Strong technical writing skills for documenting manufacturing processes and validation reports. Why ...

DPS Group

Project Architect

Cary, NC · On-site

$76K - $102K/yr

Good report and technical writing skills a requirement with proficiency in Microsoft Word, Excel ... Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology ...

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

Biotech Technical Writer information

See Raleigh, NC salary details

$13

$37

$64

How much do biotech technical writer jobs pay per hour?

As of Jun 13, 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 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 in the Biotech Technical Writer position, and why are they important?

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 job?

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 most commonly searched types of Biotech Technical Writer jobs in Raleigh, NC? The most popular types of Biotech Technical Writer jobs in Raleigh, NC are:
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What cities near Raleigh, NC are hiring for Biotech Technical Writer jobs? Cities near Raleigh, NC with the most Biotech Technical Writer job openings:
Biotech Technical Writer jobs near you
Infographic showing various Biotech Technical Writer job openings in Raleigh, NC as of June 2026, with employment types broken down into 24% Full Time, 7% Temporary, 61% Contract, and 8% Nights. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $78,739 per year, or $37.9 per hour.

Process Engineer III

Novartis Group Companies

Durham, NC

$98K - $183K/yr

Other

Medical, Life, Retirement, PTO

Posted 16 days ago

Job description

Job Description Summary

Step into a pivotal engineering role where your expertise directly shapes advanced manufacturing operations. As a Process Engineer III, you will support the design, validation, maintenance, and lifecycle management of manufacturing equipment, facilities, and utilities. This role requires hands-on experience with automated and manual visual inspection systems and drug product/fill-finish equipment to ensure compliant, reliable, and efficient GMP operations.


Job Description

Location:

  • This position will be located in Durham, NC and will be an onsite role.
  • Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

  • Bachelor's degree in Chemical, Electrical, or Mechanical Engineering or related technical field
  • Minimum 5 years pharmaceutical or biopharmaceutical GMP manufacturing experience, or equivalent experience
  • Strong knowledge of FDA regulations and GMP systems
  • Demonstrated experience supporting engineering activities in a regulated pharmaceutical or biotechnology environment
  • Experience with automated and manual visual inspection equipment, as well as general drug product / fill-finish production equipment
  • Proven ability to lead cross-functional teams in a fast-paced and dynamic setting
  • Strong project management skills with experience in both strategic and long-term planning
  • Excellent written and verbal communication skills with strong technical writing capabilities
  • Ability to analyze complex issues and implement effective, compliant engineering solutions

Essential Requirements:

  • Bachelor's degree in Chemical, Electrical, or Mechanical Engineering or related technical field
  • Minimum 5 years pharmaceutical or biopharmaceutical GMP manufacturing experience, or equivalent experience
  • Strong knowledge of FDA regulations and GMP systems
  • Demonstrated experience supporting engineering activities in a regulated pharmaceutical or biotechnology environment
  • Proven ability to lead cross-functional teams in a fast-paced and dynamic setting
  • Strong project management skills with experience in both strategic and long-term planning
  • Excellent written and verbal communication skills with strong technical writing capabilities
  • Ability to analyze complex issues and implement effective, compliant engineering solutions

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $98,700 and $183,300 annually

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

#LI-Onsite


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$98,700.00 - $183,300.00


Skills Desired

Business Continuity, Change Control, Cost Management, Data Analytics and Digital, Engineering Technical Expertise, GDP Knowledge, gmp knowledge, HSE Knowledge, Knowledge Of Relevant Tools And Systems, Manufacturing Process (Production), Operational Excellence, Quality Compliance, Resilience and Risk Management, Total Productive Maintenance

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