ZipRecruiter

Log In

1

Biotech Operator Jobs Near Me

InfoTree

Be Seen First

Specialist Technical Writing

New Albany, OH · On-site

$35 - $40/hr

... Operating Procedures (SOP'S), protocols, technical reports, and training material in a GMP ... Experience working in GMP pharma and/or biotechnology industry. Experience in a Good Manufacturing ...

New

Hyperion Biotechnology

Water Collector

Columbus, OH · On-site

$20 - $25/hr

TASKS DESCRIPTIONCollect water samples from VA facilities following standard operating procedures ... Citizen COMPANY OVERVIEWHyperion Biotechnology, Inc. has been providing services to federal ...

New

Hyperion Biotechnology

Water Collector

Columbus, OH · On-site

$20 - $25/hr

TASKS DESCRIPTION * Collect water samples from VA facilities following standard operating ... Citizen COMPANY OVERVIEW Hyperion Biotechnology, Inc. has been providing services to federal ...

New

Hyperion Biotechnology, Inc.

Water Collector

Columbus, OH

$16.50 - $22/hr

TASKS DESCRIPTION * Collect water samples from VA facilities following standard operating ... Citizen COMPANY OVERVIEW Hyperion Biotechnology, Inc. has been providing services to federal ...

New

JLL

Senior Facilities Manager

Columbus, OH · On-site

Maintain comprehensive documentation including standard operating procedures, maintenance records ... pharmaceutical, biotech, or similarly regulated environments * Demonstrated expertise in GMP ...

next page

Showing results 1-20

All JobsBiotech Operator JobsBiotech Operator Jobs Near Me

Biotech Operator information

See salary details

$10

$20

$29

How much do biotech operator jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for biotech operator in the United States is $20.07, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $22.12 per hour, depending on experience, location, and employer.
What are popular job titles related to Biotech Operator jobs? For Biotech Operator jobs, the most frequently searched job titles are:
What job categories do people searching Biotech Operator jobs look for? The top searched job categories for Biotech Operator jobs are:
Biotech Operator jobs near you
A map of the United States highlighting the number of Biotech Operator job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Biotech Operator 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 today. 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