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Internship Biotech Technical Writer Jobs (NOW HIRING)

Lancesoft

CMC Technical Writer

Ridgefield, CT · On-site

$54 - $55.70/hr

Required • Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical ... technical writing skills • High attention to detail and scientific rigor • Effective ...

Lancesoft

Technical Writer

High Point, NC · On-site

$27/hr

Required Experience Minimum 2 years of experience in a GMP-regulated pharmaceutical, biotechnology ... Knowledge, Skills, and Abilities Advanced technical writing and documentation skills. Strong ...

Actalent

Technical Writer

Somerset, NJ · On-site

Technical Writer (Manufacturing / Engineering Focus) This onsite Technical Writer role focuses on ... Internship, co-op, or early career experience in manufacturing or engineering. * Experience ...

Experic LLC

Technical Writer - Operations

Cranbury, NJ · On-site

$80K - $110K/yr

Bachelor's degree preferred in Life Sciences, Engineering, Technical Writing, or related field; equivalent experience may be considered. * 3+ years of experience in a pharmaceutical, biotechnology ...

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

As of Jul 4, 2026, the average hourly pay for internship 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.
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Internship Biotech Technical Writer jobs near you
Infographic showing various Internship Biotech Technical Writer job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.
Deviation Writer/Technical Writer (Pharmaceutical)

Deviation Writer/Technical Writer (Pharmaceutical)

Intellectt INC

Fishers, IN • On-site

Contractor

Posted 22 days ago

Job description

Hello,
I hope you’re doing well.
My name is Jayadev, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Deviation Writer/Technical Writer (Pharmaceutical)
based in Fishers, Indiana  with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at  jayadev.g@intellectt.com
 

Position: Deviation Writer
Location: Fishers, IN

Job Summary

Seeking an experienced Deviation Writer to support GMP manufacturing operations by investigating deviations, non-conformances, and quality events. The role involves root cause analysis, CAPA development, technical writing, and collaboration with cross-functional teams.

Key Responsibilities

  • Write and investigate GMP deviations, non-conformances, and quality events.
  • Gather facts, review data, and determine root causes.
  • Perform Root Cause Analysis using 5 Why and Fishbone methodologies.
  • Develop and document CAPAs (Corrective and Preventive Actions).
  • Review historical deviations and identify trends.
  • Prepare clear and detailed investigation reports.
  • Collaborate with Manufacturing, Quality, Engineering, MS&T, and Supply Chain teams.
Required Qualifications
  • Bachelor's degree in Science, Engineering, or related field.
  • 4+ years of technical writing experience in a GMP-regulated environment.
  • Strong knowledge of GMP, deviation investigations, CAPA, and quality systems.
  • Experience with eQMS/EDMS systems.
  • Proficiency in Microsoft Word and Excel.
Must-Have Skills
  • Deviation Investigation Writing
  • GMP Manufacturing Experience
  • Root Cause Analysis (5 Why, Fishbone)
  • CAPA Development
  • Technical Writing
  • Pharmaceutical/Biotech Industry Experience
  • Quality Systems (eQMS, EDMS)
  • Cross-Functional Collaboration
    Thanks Regards,
    JAYADEV
    Sourcing Specialist
    Phone  (732)-997-6982   Ext: 308
    Email jayadev.g@intellectt.com