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Overnight Biotech Technical Writer Jobs (NOW HIRING)

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Technical Writer

Springfield, NJ · On-site

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 ...

Integrated Resources INC

Technical Writer

Cambridge, MA · On-site

... biotechnology or pharmaceutical industry Direct experience in GXP-compliant quality systems is ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;

Kelly Services

Technical Writer

Petaluma, CA

$60 - $70/hr

Technical Writer (FDA/GMP Documentation) Location: Petaluma, CA (100% Onsite) Pay: $60 - $70/hour ... Experience supporting pharmaceutical, biotechnology, medical device, food manufacturing, or similar ...

Kinetic Personnel Group

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Technical Writer (ONSITE CONTRACT)

Tustin, CA · On-site

$45 - $60/hr

Experience in a biopharmaceutical, pharmaceutical, medical device, biotechnology, or other regulated manufacturing environment preferred. * Strong technical writing, editing, proofreading, and ...

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Overnight Biotech Technical Writer information

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$13

$38

$66

How much do overnight biotech technical writer jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for overnight 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 Overnight Biotech Technical Writer vs Biotech Scientific Writer?

AspectOvernight Biotech Technical WriterBiotech Scientific Writer
CredentialsBachelor's degree in life sciences or related field; technical writing experienceMaster's or PhD in life sciences; scientific research background
Work EnvironmentFast-paced biotech companies, often overnight shifts for global teamsResearch labs, academic institutions, or biotech firms, typically daytime hours
Employer & Industry UsageCommon in biotech firms requiring 24/7 documentation supportUsed in research-focused roles, less common in overnight settings

Overnight Biotech Technical Writers focus on creating clear documentation for biotech products during overnight shifts, often requiring quick turnaround and technical expertise. Biotech Scientific Writers generally work on research papers and scientific content during regular hours, with a stronger emphasis on research background. The roles overlap in industry but differ mainly in work hours and specific focus areas.

What cities are hiring for Overnight Biotech Technical Writer jobs?

Cities with the most Overnight 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 Overnight Biotech Technical Writer jobs?

States with the most job openings for Overnight Biotech Technical Writer jobs include:

Overnight Biotech Technical Writer jobs near you

Technical Writer

Stark Pharma Solutions Inc

Swiftwater, PA • On-site

Contractor

Re-posted 5 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Technical Writer

Location: Swiftwater, PA

Duration: 6-Month Contract

Industry: Pharmaceutical / Biotech Manufacturing

Position Overview

We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical and quality-related content into user-friendly training materials and documentation. This role will work closely with cross-functional teams to create compliant documentation, training content, and process materials within a GMP-regulated environment.

The ideal candidate will have experience in technical writing, quality systems documentation, and digital system deployments within pharmaceutical, biotechnology, laboratory, or manufacturing environments.

Key Responsibilities

  • Develop, revise, and maintain technical documentation, training materials, and process-related content.
  • Convert technical and operational information into engaging training presentations, user guides, and instructional materials.
  • Review, edit, and update quality documents including:
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Guidelines
  • Validation Master Plans
  • Quality System Documentation
  • Ensure all documentation complies with GMP, regulatory, and internal quality requirements.
  • Collaborate with Quality, IT, Laboratory, and Operations teams to gather information and create accurate documentation.
  • Support digital transformation initiatives by developing training materials for new system implementations.
  • Assist with document control activities and quality documentation updates.
  • Create visual content, process flows, diagrams, and presentations using PowerPoint and Visio.
  • Participate in training development and delivery activities as needed.

Required Qualifications

  • Bachelor's degree required; advanced degrees (Master's or PhD) are welcome.
  • Minimum 2+ years of experience in Technical Writing, Documentation Management, or a related role.
  • Experience working within GMP-regulated pharmaceutical, biotech, laboratory, or life sciences environments.

Hands-on experience with quality systems and applications such as:

  • Veeva
  • LIMS
  • LabWare (preferred)

Proficiency with:

  • Microsoft Word
  • Excel
  • PowerPoint
  • Visio
  • Outlook
  • Strong technical writing, editing, and document management skills.
  • Excellent verbal and written communication abilities.
  • Strong interpersonal skills with the ability to work effectively in cross-functional teams.