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

Valspec

Validation Engineer (CSV)

Seattle, WA

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

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

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$15

$44

$75

How much do biotech technical writer jobs pay per hour?

As of Aug 14, 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 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 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 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 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:

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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 64% Full Time, 11% Part Time, and 25% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $92,181 per year, or $44.3 per hour.

Lead Validation Engineer (CSV / DeltaV)

Stark Pharma Solutions Inc

Seattle, WA • On-site

Contractor

Posted 16 days ago

Job description

Position: Lead Validation Engineer (CSV / DeltaV)
Location: Seattle, WA
Duration: Long Term

Job Overview

We are seeking a Lead Validation Engineer (CSV / DeltaV) to support a major biologics manufacturing operation in the Seattle area. The ideal candidate will have extensive experience in Computer System Validation (CSV), hands-on expertise with DeltaV systems, and a proven track record leading validation activities in GMP-regulated pharmaceutical or biotechnology environments. This role involves technical leadership, validation planning, protocol development, execution, and collaboration with cross-functional teams to ensure compliant system implementation and operation.

Key Responsibilities

  • Lead Computer System Validation (CSV) activities for DeltaV-based manufacturing systems.
  • Develop and execute Validation Plans, Risk Assessments, Requirements Traceability Matrices (RTMs), IQ/OQ/IOQ Protocols, and Validation Summary Reports.
  • Support DeltaV system implementations, upgrades, expansions, and modifications.
  • Review and approve engineering documentation, functional specifications, design specifications, and configuration documents.
  • Coordinate validation activities across Automation, Engineering, Manufacturing, IT, and Quality teams.
  • Lead protocol execution, deviation investigations, issue resolution, and documentation closeout.
  • Support change control activities and validation impact assessments.
  • Provide technical guidance and mentorship to junior validation engineers.
  • Drive risk-based validation and software assurance practices aligned with GAMP 5 and current industry standards.
  • Support startup, commissioning, qualification, and operational readiness activities.
  • Participate in project planning, scheduling, resource coordination, and stakeholder communications.

Required Qualifications

  • Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related technical discipline.
  • 8+ years of Computer System Validation (CSV) experience within GMP-regulated pharmaceutical or biotechnology environments.
  • Hands-on validation experience with DeltaV systems is required.
  • Experience leading validation projects and coordinating cross-functional teams.
  • Strong experience developing and executing Validation Plans, Risk Assessments, RTMs, IQ/OQ Protocols, and Validation Summary Reports.
  • Strong knowledge of GAMP 5, CSA/CSV methodologies, 21 CFR Part 11, Data Integrity principles, and GMP documentation practices.
  • Experience supporting biologics or pharmaceutical manufacturing facilities.
  • Experience with DeltaV Batch, MES platforms, manufacturing automation systems, infrastructure qualification, and Commissioning & Qualification (C&Q) activities is highly desirable.
  • Previous experience serving as a Validation Lead or Project Lead or working in a consulting environment is a plus.
  • Excellent technical writing, communication, leadership, and client-facing skills.