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

Electrical Department Manager

Cary, NC · On-site

$113K - $145K/yr

... Biotechnology engineering project design & delivery. If you're a seasoned leader in the field, we ... Providing Technical Guidance and Solutions to the electrical department, and clients * Mentoring ...

Java Developer

Cary, NC · On-site

$47.25 - $61.25/hr

Hands-on technical role focused on Java development and business analysis in laboratory informatics ... The role involves configuring, implementing, and supporting solutions, writing Jira stories, and ...

Java Developer

Cary, NC · On-site

$47.25 - $61.25/hr

Hands-on technical role focused on Java development and business analysis in laboratory informatics ... The role involves configuring, implementing, and supporting solutions, writing Jira stories, and ...

Patent Agent

Durham, NC · On-site

$108K - $149K/yr

... biotechnology, including plant traits, microbial products, agriculture biologics, or related platforms. * Strong technical writing and analytical skills, with the ability to clearly articulate ...

Process Engineer III

Durham, NC · On-site

$98K - $183K/yr

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

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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 14, 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:
What are popular job titles related to Biotech Technical Writer jobs in Raleigh, NC? For Biotech Technical Writer jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Biotech Technical Writer jobs? Cities near Raleigh, NC with the most Biotech Technical Writer job openings:
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.
Scientist III - Biotech - CE , icIEF , HPLC

Scientist III - Biotech - CE , icIEF , HPLC

Alcami Corporation

Durham, NC

Full-time

Posted 9 days ago


Alcami rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz


Job description

 

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

The Scientist III is accountable for driving results in a fast-paced environment by performing analytical-biotech routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Scientist III may also be required to work on method development/method validation projects. For this position, HPLC, CE, icIEF, and UV based methodologies are commonly employed in the described testing. Other key methodologies applied include cKF/KF, pH and osmolality. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company).

On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 5:00pm.
Responsibilities
  • Develops, validates and transfers analytical methodology for analysis via HPLC (SEC, AEX, CEX), UV, CE and icIEF.
  • Performs GMP review of solutions and wet chemical analyses and chromatography.
  • Performs one or more of the following techniques: HPLC, UV, CE and icIEF.
  • Evaluates and interprets generated data.
  • Analyzes information for technical correctness and accuracy.
  • Understands the theoretical basis of methods/experiments.
  • Solves problems of diverse scope in which analysis of data requires evaluation of identifiable factors.
  • Writes test procedures, protocols, and reports.
  • Maintains working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
  • Assists in removal of hazardous waste, routine equipment cleaning, and restocking of consumable products and reagents.
  • Effectively uses various laboratory software packages (Empower3, ProCal, Master Control, ELN, etc.).
  • Maintains a safe, clean, and organized work environment free of safety hazards.
  • Safely handles potent compounds.
  • This position will be required to supervise, handle, or process hazardous waste under Resource and Conservation guidelines promulgated under 40 CFR 262.177(a)(7), Personnel Training. This includes completion of initial and annual RCRA training and documented as required in Alcami records. This training also includes familiarity with emergency response procedures, emergency equipment, and emergency systems.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Other duties as assigned.
Qualifications
  • Associate's degree and 16+ years of related experience.
  • Bachelor's degree and 6+ years of related experience.OR
  • Master's degree with 2+ years of related experience required or PhD with 0+ year of experience.
  • Experience in Pharmaceutical, CDMO, or cGMP required.
Knowledge, Skills, and Abilities
  • Hands on CE and HPLC experience required. 
  • Excellent verbal and written communication and documentation skills required.
  • Excellent detail orientation and organizational skills required.
  • Excellent problem-solving and basic trouble-shooting ability required.
  • Excellent knowledge of Laboratory equipment and safety required.
  • Expert knowledge of Laboratory Documentation is required.
  • Working knowledge of cGMP in a pharmaceutical or regulated environment required.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
  • Empower experience strongly preferred. 
Travel Expectations
  • Up to 5% domestic travel.
Physical Demands and Work Environment

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand. The employee is occasionally required to walk; sit and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.

While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and the risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

Employment Type: FULL_TIME