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Manufacturing Technical Writer Jobs in Raleigh, NC

Technical Writer

Durham, NC ยท On-site

$64 - $69/hr

Bachelors Responsibilities As a member of Manufacturing Sciences, the Technical Writer will provide written documentation expertise to the clinical and commercial manufacturing campaigns run at the ...

Speakers/Writers

Cary, NC ยท On-site

$15 - $60/hr

Current Labelbox customers are transforming industries within insurance, retail, manufacturing ... technical writer, editor, or similar roles. - Interest in AI and machine learning concepts.

Strong technical writing skills for documenting manufacturing processes and validation reports. Why Join Us? Opportunity to work on cutting-edge drug manufacturing processes. Hands-on experience in a ...

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Manufacturing Technical Writer information

See Raleigh, NC salary details

$13

$37

$64

How much do manufacturing technical writer jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for manufacturing 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 key skills and qualifications needed to thrive in the Manufacturing Technical Writer position, and why are they important?

A Manufacturing Technical Writer should possess strong writing, editing, and document management skills, often supported by a degree in technical communication, engineering, or a related field. Familiarity with authoring tools such as Adobe FrameMaker, MadCap Flare, and knowledge of Document Control Systems (DCS) or Product Lifecycle Management (PLM) are commonly required, along with certifications like CPTC. Excellent communication, attention to detail, and the ability to quickly grasp complex manufacturing processes make candidates stand out. These competencies ensure technical documentation is accurate, clear, and effectively supports safe and efficient manufacturing operations.

What are the typical daily responsibilities of a Manufacturing Technical Writer?

As a Manufacturing Technical Writer, your daily responsibilities typically include researching complex machinery or production processes, creating and updating instruction manuals, standard operating procedures, and safety documentation. You will frequently collaborate with engineers, production managers, and quality assurance teams to gather accurate information and ensure documentation reflects current practices. Reviewing and testing documents for clarity and usability, maintaining version control, and complying with industry or regulatory standards are also central to the role. This position requires a proactive approach to communication and a commitment to continuous improvement in documentation practices.

What is a Manufacturing Technical Writer job?

A Manufacturing Technical Writer creates clear and concise documentation for manufacturing processes, equipment, and standards. They develop user manuals, work instructions, and technical guides to ensure accurate production and compliance. Their role involves collaborating with engineers, operators, and quality teams to translate complex technical details into understandable content. Strong writing, technical expertise, and attention to detail are essential for success in this role.

What are the most commonly searched types of Manufacturing Technical Writer jobs in Raleigh, NC? The most popular types of Manufacturing Technical Writer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Manufacturing Technical Writer jobs? Cities near Raleigh, NC with the most Manufacturing Technical Writer job openings:
Infographic showing various Manufacturing Technical Writer job openings in Raleigh, NC as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $78,739 per year, or $37.9 per hour.
Technical Writer

Technical Writer

Randstad

Durham, NC โ€ข On-site

$64 - $69/hr

Full-time

Posted 12 days ago


Job description

๏‚ท Life Science background with at least 5 years experience is preferred.๏‚ท Good communication and project management skills appropriate for leadership of techtransfer projects๏‚ท Working knowledge in technical understanding of Parenteral Filling Operations (e.g.Filling Isolator, Lyophilizer, Visual Inspection) including transfer of such processes intofull-scale drug product manufacturing facilities๏‚ท Excels at working in a team environment๏‚ท Comfortable analyzing scientific datasets/analytical skills with excellent written skills๏‚ท Ability to work independently and support a large cross-functional group๏‚ท Some knowledge of cGMP, FDA/EMA regulations, Process Performance Qualification,Continued Process Verification

salary: $64 - $69 per hour
shift: First
work hours: 8 AM - 4 PM
education: Bachelors

Responsibilities

As a member of Manufacturing Sciences, the Technical Writer will provide written
documentation expertise to the clinical and commercial manufacturing campaigns run at the
Parenteral Facility RTP Pharma Site. The focus of this position will be as a key leader for
investigations and project implementation for Manufacturing Sciences using their technical
expertise on fill/finish, visual inspection, and packaging.
The incumbent will be tasked with writing PPQ Protocols, PPQ Reports, data verification
activities for confirmation of source data for reports, preliminary writing for sections of the filing.
Creating the Master Sample Matrix (MSM) for Manufacturing personnel to be used for on the
production floor activities.
Qualifications/Education:
๏‚ท Life Science background with at least 5 years experience is preferred.
๏‚ท Good communication and project management skills appropriate for leadership of tech
transfer projects
๏‚ท Working knowledge in technical understanding of Parenteral Filling Operations (e.g.
Filling Isolator, Lyophilizer, Visual Inspection) including transfer of such processes into
full-scale drug product manufacturing facilities
๏‚ท Excels at working in a team environment
๏‚ท Comfortable analyzing scientific datasets/analytical skills with excellent written skills
๏‚ท Ability to work independently and support a large cross-functional group
๏‚ท Some knowledge of cGMP, FDA/EMA regulations, Process Performance Qualification,
Continued Process Verification


Skills
  • Technical
  • life science
  • cGMP

  • Qualifications
  • Years of experience: 5 years
  • Experience level:

  • Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.


    Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
    Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
    This posting is open for thirty (30) days.