Technical Writer - Pharma / GMP Environment Location: Swiftwater, PA (Fully Onsite) We are actively ... biotech, analytical, or manufacturing environments • Excellent written and verbal communication ...
Technical Writer - Pharma / GMP Environment Location: Swiftwater, PA (Fully Onsite) We are actively ... biotech, analytical, or manufacturing environments • Excellent written and verbal communication ...
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Quick apply
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Job ID: 21-12907 Skills: -Ability to write technical documents, and tenacious attention to detail ... in the biotech or pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad ...
Job ID: 21-12907 Skills: -Ability to write technical documents, and tenacious attention to detail ... in the biotech or pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad ...
Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. Experience writing technical documentation, including ...
Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. Experience writing technical documentation, including ...
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 ...
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 ...
Technical Writer SwiftWater, PA - Onsite 9+ Months Role will work with a team on a new digital ... or biotech environment) * Must possess sound interpersonal and information gathering skills, be ...
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Technical Writer SwiftWater, PA - Onsite 9+ Months Role will work with a team on a new digital ... or biotech environment) * Must possess sound interpersonal and information gathering skills, be ...
Near New Brunswick, NJ Join a leading Contract Development and Manufacturing Organization (CDMO) supporting the pharmaceutical and biotechnology industries! Position Summary As a Technical Writer ...
Near New Brunswick, NJ Join a leading Contract Development and Manufacturing Organization (CDMO) supporting the pharmaceutical and biotechnology industries! Position Summary As a Technical Writer ...
Digital Technical Writer
Texas City, TX · On-site
Serve as mentor to interns. Digital Technical Writer Mandatory Skills * Strong interpersonal communication skills in both developing collaborative relationships with SME and work with a wide range of ...
Digital Technical Writer
Texas City, TX · On-site
Serve as mentor to interns. Digital Technical Writer Mandatory Skills * Strong interpersonal communication skills in both developing collaborative relationships with SME and work with a wide range of ...
Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development ... Strong organization and technical writing skills * High attention to detail and scientific rigor
Quick apply
Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development ... Strong organization and technical writing skills * High attention to detail and scientific rigor
Senior Technical Writer
Holland, MI · On-site
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Senior Technical Writer
Holland, MI · On-site
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Technical Writer- LabVantage
Indianapolis, IN · On-site +1
Generate AI-accelerated draft documentation and testing outputs Required Qualifications: * 5+ years of technical writing experience in GMP-regulated pharma or biotech environments * Hands-on ...
Technical Writer- LabVantage
Indianapolis, IN · On-site +1
Generate AI-accelerated draft documentation and testing outputs Required Qualifications: * 5+ years of technical writing experience in GMP-regulated pharma or biotech environments * Hands-on ...
Senior Technical Writer
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Senior Technical Writer
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Senior Technical Writer
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Senior Technical Writer
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Senior Technical Writer
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Senior Technical Writer
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Technical Writer-LMS Administrator
Bronx, NY · On-site
$75K - $80K/yr
The Technical Writer will partner with Quality department, other cross functional managers ... Possesses basic technical knowledge and background in the pharmaceutical and biotechnology industry
Technical Writer-LMS Administrator
Bronx, NY · On-site
$75K - $80K/yr
The Technical Writer will partner with Quality department, other cross functional managers ... Possesses basic technical knowledge and background in the pharmaceutical and biotechnology industry
Senior Technical Writer
Holland, MI · On-site
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
Senior Technical Writer
Holland, MI · On-site
$87K - $127K/yr
Foundational knowledge of technical writing principles or structured content practices through coursework, internships, or professional experience. * Certification in technical communication or ...
We are currently seeking a Technical Writer Intern to support the creation and improvement of ... This internship is part-time and is estimated to last for approximately 10 weeks. Compensation: $24 ...
We are currently seeking a Technical Writer Intern to support the creation and improvement of ... This internship is part-time and is estimated to last for approximately 10 weeks. Compensation: $24 ...
We are currently seeking a Technical Writer Intern to support the creation and improvement of ... This internship is part-time and is estimated to last for approximately 10 weeks. Compensation: $24 ...
We are currently seeking a Technical Writer Intern to support the creation and improvement of ... This internship is part-time and is estimated to last for approximately 10 weeks. Compensation: $24 ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
... biotech acceptable). * 3+ years of people leadership experience, including managing writers ... Prior leadership of technical writing teams within a medical device organization. * Extensive ...
Internship Biotech Technical Writer information
See salary details
$13.70 - $18.47
2% of jobs
$18.47 - $23.23
7% of jobs
$23.23 - $27.99
12% of jobs
$29.11 is the 25th percentile. Wages below this are outliers.
$27.99 - $32.76
16% of jobs
The median wage is $36.33 / hr.
$32.76 - $37.52
17% of jobs
$37.52 - $42.29
14% of jobs
$45.38 is the 75th percentile. Wages above this are outliers.
$42.29 - $47.05
11% of jobs
$47.05 - $51.81
10% of jobs
$51.81 - $56.58
5% of jobs
$56.58 - $61.34
3% of jobs
$61.34 - $66.11
3% of jobs
$13
$38
$66
How much do internship biotech technical writer jobs pay per hour?
As of Jun 8, 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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Job description
Job Title: Technical Writer – Pharma / GMP Environment
Location: Swiftwater, PA (Fully Onsite)
Job Description:
We are actively seeking an experienced Technical Writer for a long-term onsite contract opportunity with one of our pharmaceutical clients in Swiftwater, PA.
The selected candidate will work closely with cross-functional teams on a new digital system implementation project focused on converting operational and scientific information into structured training materials and technical documentation.
Key Responsibilities:
• Design, develop, review, and update technical documentation and training materials
• Assist in editing quality documents including SOPs, guidelines, validation master plans, and related documentation
• Ensure all documentation complies with GMP and regulatory requirements
• Create engaging PowerPoint training materials, slides, graphics, and presentations
• Collaborate with business and technical teams to gather and organize information
• Support digital system deployment and documentation activities
Required Qualifications:
• Bachelor’s degree required (Master’s or PhD candidates welcome)
• Minimum 2+ years of experience as a Technical Writer
• Experience working with quality applications such as Veeva, LIMS, LabWare, etc.
• Strong experience with MS Office Suite (Word, Excel, PowerPoint, Visio, Outlook)
• Prior experience in GMP pharmaceutical, biotech, analytical, or manufacturing environments
• Excellent written and verbal communication skills
• Strong interpersonal and team collaboration skills
• Ability to create professional training materials and presentations
Preferred Qualifications:
• Background in Digital IT or Scientific domains
• Experience with QC (Quality Control) activities
• Experience deploying digital systems
• Knowledge of validation processes and compliance documentation