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Biotech Technical Writer Jobs Near Me

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Specialist Technical Writing

New Albany, OH · On-site

$35 - $40/hr

Experience working in GMP pharma and/or biotechnology industry. Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing. Experience with device ...

New

PSC Biotech

Validation Engineer

Columbus, OH · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... technical troubleshooting and analytical skills. Excellent written and verbal communication skills ...

Ultimate Solutions

C&Q Engineer, Sr.

Columbus, OH · On-site

$100K - $138K/yr

Experience with automation systems, process equipment, and utilities in pharmaceutical or biotechnology manufacturing. * Excellent technical writing, analytical, and organizational skills. * Strong ...

Astrix Inc

Senior Maintenance Technician

New Albany, OH · On-site

$25 - $30/hr

Pay Rate Low: 25 | Pay Rate High: 30 Our client, a renowned leader in biotechnology, is ... Strong documentation and technical writing skills. * Excellent organizational, communication, and ...

Amgen, Inc.

Sr Mechanical Engineer

New Albany, OH · On-site

$100K - $132K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Technical writing skills Competencies: * Established Leadership capabilities * Passion for ...

Amgen

Sr Mechanical Engineer

New Albany, OH · On-site

$100K - $132K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Technical writing skills Competencies: * Established Leadership capabilities * Passion for ...

Ultimate Solutions

C&Q Engineer, Lead

Columbus, OH · On-site

$99K - $130K/yr

... biotechnology, medical devices, and logistics markets. Description ... The Commissioning and Qualification (C&Q) Lead will join a highly technical team for a start-up ...

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How much do biotech technical writer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for 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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Biotech Technical Writer jobs near you
A map of the United States highlighting the number of Biotech Technical Writer job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Biotech Technical Writer job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Manufacturing Technical Writer

Infotree Global Solutions

New Albany, OH • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Preferred: B.S. 2+ YOE would be ideal, previous Veeva experience, and prior deviation and CAPA experience.


What you will do

In this role you will support the manufacturing team and provide technical expertise to regularly draft and revise documents such as Standard Operating Procedures (SOP'S), protocols, technical reports, and training material in a GMP regulated environment that supports the manufacturing process.


Develop, review, and update technical content including but not limited to standard operating procedures, work instructions, risk assessments, protocols & reports for manufacturing team.

Provide technical and clerical support to the manufacturing team in the preparation of documentation, collation of data and tracking of technical documents.

Liaise with manufacturing team and other cross functional departments regarding documentation changes in an effective and timely manner.

Collaborate with multiple departments to support new/revise training documentation for manufacturing staff.

Support process owners and participate in continuous process improvement and / or troubleshooting projects.

Support manufacturing team in reducing document turnaround times.

Ensure documentation related actions are completed on time and current schedule is maintained, accurate, and up to date.

Develop protocols for Manufacturing to support change controls, deviations & troubleshooting investigations with provision from relevant SMEs.

Generate, own, and provide subject matter expertise to Quality System records as minor deviations, CAPA and change control records.

Track pending activities required to support change control implementations.

Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current operating systems.

Share knowledge with members of the manufacturing team.


Basic Qualifications:

Master's Degree in Science and/or Engineering.

Or

Bachelor's Degree in Science and/or Engineering and 2 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.

Or

Associate’s Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.

Or

High School Diploma / GED and 8 years in Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.


Preferred Qualifications:

Educational Background in Science and/or Engineering.

Experience working in GMP pharma and/or biotechnology industry.

Experience in a Good Manufacturing Practices (GMP) environment and demonstrated background in technical writing.

Experience with device assembly and packaging of final product.

Ability to translate highly technical information into easily understandable information for manufacturing operators.

Dynamic skills and usage of photographs, drawings, diagrams, animation, and charts that increase users’ understanding.

Experience supporting deviations, investigations, CAPA’s and change controls.

A fact-based problem solver with strong troubleshooting and problem-solving skills.

Pro-active with the ability to prioritize work to meet benchmarks

Good documentation and communication


Top 3 Must Have Skill Sets:

GMP background

Prior deviation/investigation ownership

Excellent written and oral communication

Apply