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Biotech Technical Writer Jobs in Seattle, WA (NOW HIRING)

Jobtailor

Automation CSV Engineer

Redmond, WA · On-site

$120 - $180/hr

Requirements * Bachelor's degree in Engineering, Computer Science, Biotechnology, Information ... Strong technical writing skills with experience authoring validation documentation and compliance ...

New

Valspec

Validation Engineer (CSV)

Seattle, WA · On-site

Valspec partners with pharmaceutical and biotechnology manufacturers to deliver compliant, reliable ... Excellent technical writing, communication, and client-facing skills. Preferred Qualifications

Valspec

Validation Engineer (CSV)

Redmond, WA · On-site

Valspec partners with pharmaceutical and biotechnology manufacturers to deliver compliant, reliable ... Excellent technical writing, communication, and client-facing skills. Preferred Qualifications

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Biotech Technical Writer information

See Seattle, WA salary details

$15

$44

$75

How much do biotech technical writer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for biotech technical writer in Seattle, WA is $44.32, according to ZipRecruiter salary data. Most workers in this role earn between $32.84 and $53.61 per hour, depending on experience, location, and employer.

What is a biotech technical writer?

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 key skills and qualifications needed to thrive as a biotech technical writer?

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 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 most commonly searched types of Biotech Technical Writer jobs in Seattle, WA?

The most popular types of Biotech Technical Writer jobs in Seattle, WA are:

What are popular job titles related to Biotech Technical Writer jobs in Seattle, WA?

For Biotech Technical Writer jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Biotech Technical Writer jobs in Seattle, WA look for?

The top searched job categories for Biotech Technical Writer jobs in Seattle, WA are:

Biotech Technical Writer jobs near you
Infographic showing various Biotech Technical Writer job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 8% Part Time, 4% Contract, and 1% Nights. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $92,181 per year, or $44.3 per hour.

Automation CSV Engineer

Jobtailor

Redmond, WA • On-site

$120 - $180/hr

Other

Posted 3 days ago

New

Job description

  • The Automation CSV Engineer is responsible for supporting validation, compliance, testing, and technical documentation activities for GMP automation systems within a regulated manufacturing environment.
  • Support validation and lifecycle management activities for GMP automation systems including DeltaV, PI, SCADA, PLC, and associated manufacturing control platforms.
  • Assist in ensuring automation systems remain compliant with GxP regulations, internal procedures, and industry standards throughout the system lifecycle.
  • Participate in implementation, upgrade, patching, migration, and change control activities for automation systems.
  • Execute and support commissioning, qualification, and validation testing activities including FAT, SAT, IQ, OQ, PQ, and automation functional testing.
  • Document test execution results, discrepancies, deviations, and corrective actions in accordance with approved procedures.
  • Collaborate with system owners and technical SMEs to gather system requirements and support risk assessments for automation systems.
  • Support periodic reviews, audit readiness activities, and inspection support for validated automation systems.
Requirements
  • Bachelor’s degree in Engineering, Computer Science, Biotechnology, Information Systems, or related technical discipline preferred.
  • Minimum of 5 years of experience supporting GMP automation systems, computer system validation (CSV), automation testing, or technical writing activities within regulated industries.
  • Hands‑on experience with automation platforms such as DeltaV, PI, SCADA, PLC, or related manufacturing systems.
  • Experience executing validation and qualification activities including FAT, SAT, IQ, OQ, PQ, and functional testing.
  • Strong technical writing skills with experience authoring validation documentation and compliance records.
  • Working knowledge of GxP regulations and industry guidance including: 21 CFR Part 11, Annex 11, GAMP 5, FDA CSA principles, Data Integrity requirements.
  • Understanding of automation system lifecycle management and pharmaceutical quality systems.
  • Experience supporting change controls, deviations, CAPAs, and risk assessments within GMP environments.
  • Strong organizational skills and attention to detail with the ability to manage multiple assignments simultaneously.
  • Effective communication and collaboration skills with the ability to work across technical and business functions.
Core Competencies

Demonstrates expertise in supporting GMP automation systems, including validation, compliance, and technical documentation, while ensuring adherence to GxP regulations and industry standards. Proficient in executing validation activities and managing automation system lifecycles within regulated environments.

Highest-signal resume keywords
  • GMP Automation Systems Support
  • Computer System Validation (CSV)
  • Validation Testing Activities (FAT, SAT, IQ, OQ, PQ)
  • Technical Writing for Validation Documentation
  • GxP Regulations Knowledge
ATS Optimization KeywordsHard Skills
  • GMP Automation Systems
  • Computer System Validation (CSV)
  • Validation Testing (FAT, SAT, IQ, OQ, PQ)
  • Technical Writing
  • Automation Platforms (DeltaV, PI, SCADA, PLC)
  • Lifecycle Management
  • Change Control
  • Risk Assessment
  • Deviation Management
  • CAPA Support
Soft Skills
  • Organizational Skills
  • Attention to Detail
  • Effective Communication
  • Collaboration Skills
Industry Keywords
  • GxP Regulations
  • 21 CFR Part 11
  • Annex 11
  • GAMP 5
  • FDA CSA Principles
  • Data Integrity
  • Pharmaceutical Quality Systems
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