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Full Time Biotech Technical Writer Jobs (NOW HIRING)

CEDENT

Technical Writer

Springfield, NJ

Experience: * Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. * Experience writing technical ...

Intuitive Surgical

Technical Writer

Sunnyvale, CA

Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...

Intuitive

Technical Writer

Sunnyvale, CA

Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...

Linchpin Solutions Inc

Technical Writer

Quantico, VA · On-site

Fulltime, On-site, Quantico, VA; limited travel as required ( Role Overview: The Technical Writer supports the MOCTT Documentation Support Services mission at the Marine Corps Tactics and Operations ...

Intuitive

Technical Writer

Sunnyvale, CA · On-site

Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...

Konik

Technical Writer

Saint Paul, MN · Hybrid

$28 - $40/hr

... full-time roles after an initial contracting period. If you're a detail-oriented Technical Writer ... passionate about creating high-quality, structured documentation for defense, aerospace, or complex ...

Linchpin Solutions Inc

Technical Writer

Quantico, VA · On-site

Fulltime, On-site, Quantico, VA; limited travel as required ( Role Overview: The Technical Writer supports the MOCTT Documentation Support Services mission at the Marine Corps Tactics and Operations ...

Adaptic LLC

Technical Writer

Fort George G Meade, MD · On-site

Meade, MD 20755 US (Primary) Category Technical Writer (TW) Salary Grade Date Needed By Job Type Full-time Travel Overview Adaptic is looking for Technical Writers to make a huge impact on the DOD ...

Lonza

MSAT Process Technical Writer

Portsmouth, NH · On-site

Working experience of pharma/biotech (or equivalent) preferred. * Technical writing in the biotech industry preferred. * Project management skills a plus. * Strong MS Word experience preferred.

SAIC

Technical Writer

North Charleston, SC

Computer Operator Schedule: Full-Time Shift: Day Job Travel: No Minimum Clearance Required: None ... ORA_ON_SITE Description SAIC is seeking a dedicated Technical Writer to join our team in support of ...

CACI International, Inc.

Technical Writer

Crane, IN

Engineering and Technical Support Time Type: Full time Minimum Clearance Required to Start: Secret ... Write technical [prototype] manuals, training manuals, and standard operating procedures for ...

SAIC

Technical Writer

MS · Remote

$80K - $120K/yr

Technical Writer/Ed Schedule: Full-Time Shift: Day Job Travel: No Minimum Clearance Required: None Clearance Level Must Be Able to Obtain: Secret Potential for Remote Work: ORA_REMOTE Description ...

AST

Technical Writer

Tacoma, WA · On-site

$30.83 - $43.27/hr

The Technical Writer will play an active role in developing, maintaining, and standardizing ... This is a full-time position based in Tacoma. *All benefits listed in this post are subject to ...

Trax

Technical Writer

Coral Gables, FL · On-site

Technical Writers are responsible for providing effective information for end users and must be ... Job type : Full time / Hourly Job Level : Intermediate Level Job Location : Fully Onsite - Coral ...

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Full Time Biotech Technical Writer information

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How much do full time biotech technical writer jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for full time biotech technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What is the difference between Full Time Biotech Technical Writer vs Full Time Medical Writer?

AspectFull Time Biotech Technical WriterFull Time Medical Writer
CredentialsBachelor's degree in life sciences, writing experienceAdvanced degree (MD, PhD), medical/scientific background
Work EnvironmentBiotech companies, research labs, CROsPharmaceutical companies, medical communications firms
Industry UsageDevelops technical documentation for biotech productsCreates clinical, regulatory, and medical education content

Full Time Biotech Technical Writers focus on creating technical documents related to biotech products, often with a background in life sciences. Full Time Medical Writers typically have advanced medical or scientific degrees and produce clinical and regulatory content for the medical and pharmaceutical industries. While both roles require strong writing skills, their focus areas and required credentials differ significantly.

What cities are hiring for Full Time Biotech Technical Writer jobs? Cities with the most Full Time Biotech Technical Writer job openings:
What are the most commonly searched types of Biotech Technical Writer jobs? The most popular types of Biotech Technical Writer jobs are:
What states have the most Full Time Biotech Technical Writer jobs? States with the most job openings for Full Time Biotech Technical Writer jobs include:
Full Time Biotech Technical Writer jobs near you
Technical Writer

Technical Writer

CEDENT

Springfield, NJ

Full-time

Posted 6 days ago

Job description

Summary: Reporting to the appropriate department based on area of expertise (Quality Assurance, Quality Control, or Manufacturing). We are seeking a detail-oriented and highly skilled GMP Pharmaceutical Technical Writer to join our team. The ideal candidate will be responsible for creating, revising, and maintaining various controlled documentation that complies with Good Manufacturing Practices (GMP) regulations and industry standards. This role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry.
Responsibilities:
  • Technical Documentation: Author, edit, and maintain a wide range of documents, including Standard Operating Procedures (SOPs), batch records, validation protocols, technical reports, change control documents, and regulatory submissions in accordance with GMP guidelines.
  • Compliance: Ensure all written materials meet regulatory and GMP requirements, and align with the company’s quality standards, procedures, and policies.
  • Collaboration: Work closely with both Client stakeholders and client stakeholders to establish alignment on deliverables and ensure project timelines are maintained.
  • Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents.
  • Process Improvement: Participate in process improvement initiatives related to document control, writing standards, and compliance, ensuring continuous enhancement of documentation practices.
  • Audits & Inspections: Support internal and external audits by preparing relevant documentation and ensuring that all technical writing adheres to current regulatory standards.
  • Change Control: Document and track changes in manufacturing processes, equipment, and methodologies, ensuring updates to procedures and records are properly reflected.
Essential Education and Qualifications:
  • Education: Bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or a related field. Advanced degree or certification in technical writing is a plus.
  • Experience:
  • Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry.
  • Experience writing technical documentation, including SOPs, validation protocols, and reports.
  • Knowledge:
  • Solid understanding of GMP regulations (FDA, EMA, ISO, ICH, etc.) and regulatory requirements for pharmaceutical manufacturing.
  • Proficiency with document management systems and Microsoft Office Suite (Word, Excel, PowerPoint).
  • Skills:
  • Exceptional written and verbal communication skills, with a strong ability to translate complex technical concepts into clear, concise documentation.
  • Detail-oriented with strong organizational and project management skills.
  • Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment.
  • Strong analytical and problem-solving skills, with the ability to work cross-functionally across departments.
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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