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Internship Biotech Technical Writer Jobs (NOW HIRING)

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

Technical Writer

Northridge, CA · On-site +1

$64K - $110K/yr

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

Technical writing experience through coursework or previous internships. * Familiarity with OSHA safety concepts. * Experience creating flowcharts or process maps. * Basic understanding of ...

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Please note that "regular employees" refers to those who are not temporary staff, such as interns ...

Our interns and new graduates work on real projects that affect how our business runs, giving them ... Technical writers in the Content Experience organization at Salesforce produce documentation and ...

... internships and academic experience count) * Strong writing, editing, and proofreading skills, with an eye for clarity and consistency * Ability to break down complex or technical information into ...

Our interns and new graduates work on real projects that affect how our business runs, giving them ... Technical writers in the Content Experience organization at Salesforce produce documentation and ...

... internships and academic experience count) * Strong writing, editing, and proofreading skills, with an eye for clarity and consistency * Ability to break down complex or technical information into ...

Our interns and new graduates work on real projects that affect how our business runs, giving them ... Technical writers in the Content Experience organization at Salesforce produce documentation and ...

Our interns and new graduates work on real projects that affect how our business runs, giving them ... Technical writers in the Content Experience organization at Salesforce produce documentation and ...

Our interns and new graduates work on real projects that affect how our business runs, giving them ... Technical writers in the Content Experience organization at Salesforce produce documentation and ...

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Internship Biotech Technical Writer information

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$13

$38

$66

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

As of Aug 15, 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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The most popular types of Biotech Technical Writer jobs are:

What states have the most Internship Biotech Technical Writer jobs?

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

Infographic showing various Internship Biotech Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 6% Part Time, 4% Contract, and 1% Nights. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Technical Writer with Security Clearance

Kelly FedSecur

Petaluma, CA • On-site

$60 - $70/hr

Contractor

Posted yesterday

New


Job description

Technical Writer (FDA/GMP Documentation) Location: Petaluma, CA (100% Onsite) Pay: $60 - $70/hour DOE Duration: Contract to Hire based on performance About the Role Our client is seeking an experienced Technical Writer to develop FDA/GMP-compliant SOPs, work instructions, forms, and process documentation in support of a critical product launch. This is a hands-on role working closely with Sales and Operations to document business processes and build audit-ready quality documentation. Responsibilities * Develop SOPs, work instructions, forms, and controlled documentation.
* Document operational workflows from customer order through product shipment.
* Create documentation for complaint handling, product traceability, and quality processes.
* Work directly with subject matter experts to capture and document existing processes.
* Ensure documentation meets FDA and GMP requirements.
* Assist with training documentation as new procedures are implemented. Minimum Qualifications * 5+ years of experience writing SOPs and controlled documentation in an FDA-regulated environment.
* Experience supporting pharmaceutical, biotechnology, medical device, food manufacturing, or similar regulated industries.
* Strong knowledge of FDA regulations and Good Manufacturing Practices (GMP).
* Proven ability to independently develop clear, audit-ready documentation.
* Excellent communication, interviewing, and organizational skills. Please note: General technical writing experience outside of FDA-regulated industries will not meet the requirements of this position. 10324968