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Biotech Manufacturing Associate Jobs in Ohio (NOW HIRING)

Amgen

Senior Associate Manufacturing I

New Albany, OH · On-site

$14.50 - $17.25/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Join us and transform the lives of patients while transforming your Manufacturing Senior Associate ...

Amgen, Inc.

Specialist, Manufacturing

New Albany, OH · On-site

Or Associate's degree and 8 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies. Or High school diploma / GED and 10 ...

Amgen

Specialist, Manufacturing

New Albany, OH

Or Associate's degree and 8 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies. Or High school diploma / GED and 10 ...

InfoTree

Be Seen First

Associate Manufacturing Systems Engineer)

New Albany, OH · On-site

$32 - $35/hr

Preferred Qualifications Experience in pharmaceutical, biotechnology, medical device, food ... Associate Manufacturing Systems Engineer is a hands-on technical problem solver who quickly ...

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All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Ohio

Biotech Manufacturing Associate information

See Ohio salary details

$11

$19

$31

How much do biotech manufacturing associate jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for biotech manufacturing associate in Ohio is $19.81, according to ZipRecruiter salary data. Most workers in this role earn between $15.53 and $22.16 per hour, depending on experience, location, and employer.

What are Biotech Manufacturing Associates?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What jobs can I get with an associate's degree in biotechnology?

Biotech Manufacturing Associates are common roles for those with an associate's degree in biotechnology, involving tasks such as preparing and operating laboratory equipment, following strict safety protocols, and documenting processes. Other positions include quality control technician, laboratory technician, and production operator, often requiring knowledge of GMP standards and familiarity with lab tools and procedures.

What does a biotech associate do?

A biotech manufacturing associate is responsible for performing tasks related to the production of biotechnological products, such as preparing equipment, following manufacturing protocols, and ensuring quality control. They often work in laboratory or cleanroom environments, using tools like bioreactors and adhering to safety and regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing, processing, and packaging biological products in a manufacturing environment. They operate equipment, follow strict safety and quality protocols, and document production activities to ensure compliance with regulatory standards. The role often requires attention to detail, knowledge of GMP practices, and the ability to work in a team setting.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by Biotech Manufacturing Associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

How much does a manufacturing associate make at KBI Biopharma?

A Biotech Manufacturing Associate at KBI Biopharma typically earns between $50,000 and $70,000 annually, depending on experience and location. The role involves working in a regulated environment, often requiring knowledge of GMP protocols and bioprocessing equipment.

What are the key skills and qualifications needed to thrive as a Biotech Manufacturing Associate, and why are they important?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.
What are popular job titles related to Biotech Manufacturing Associate jobs in Ohio? For Biotech Manufacturing Associate jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Biotech Manufacturing Associate jobs in Ohio look for? The top searched job categories for Biotech Manufacturing Associate jobs in Ohio are:
What cities in Ohio are hiring for Biotech Manufacturing Associate jobs? Cities in Ohio with the most Biotech Manufacturing Associate job openings:
Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Ohio as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 24% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $41,204 per year, or $19.8 per hour.
Manufacturing Automation Engineer - Packaging Systems (Rockwell PLC / GMP)

Manufacturing Automation Engineer - Packaging Systems (Rockwell PLC / GMP)

3 Key Consulting

New Albany, OH • On-site

$32 - $35/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Manufacturing Automation Engineer - Packaging Systems (Rockwell PLC / GMP) - (JP15435) Location: New Albany, OH. 43054 Employment Type: Contract Business Unit: AOH Manufacturing Systems Engineering Duration: 6+ months (with likely extensions and/or conversion to permanent) Posting Date: 06/2/26 Pay Rate: $32 - $35/hour W2 Notes: Only qualified candidates need apply.Fully Onsite - Standard Hours 3 Key Consulting is hiring a Manufacturing Automation Engineer - Packaging Systems (Rockwell PLC / GMP) for a consulting engagement with our direct client, a leading global biopharmaceutical company. Position Overview: This Engineer role reports to the Engineering & Maintenance organization and supports commercial GMP Final Drug Product (FDP) manufacturing operations at the client's advanced assembly and packaging facility in New Albany, Ohio. The position applies advanced engineering and automation principles to packaging systems, manufacturing equipment, process optimization, troubleshooting, and continuous improvement initiatives. Approximately 15% travel may be required. Why is the Position Open? Planned Project Top Must Have Skills:
  • PLC proficiency, specifically Rockwell / Allen-Bradley
  • Experience troubleshooting and repairing manufacturing/process equipment
  • Strong communication skills
  • Hands-on automation and equipment support experience preferred
Key Responsibilities: Packaging Line & Manufacturing Support
  • Support commercial production packaging lines in a GMP-regulated manufacturing environment
  • Provide technical operations support to improve line performance, reliability, and capacity
  • Partner with Engineering, Maintenance, Manufacturing, Quality, and cross-functional teams to implement technical improvements
  • Support complex manufacturing, process optimization, scale-up, and continuous improvement initiatives
Automation System Design & Integration
  • Design and develop automation systems and control strategies for packaging machinery and manufacturing processes
  • Implement and configure PLCs, HMIs, and related automation equipment
  • Integrate new automation technologies into existing packaging systems
  • Create and maintain system specifications, design documents, operational procedures, and technical documentation
Troubleshooting & Technical Support
  • Diagnose and resolve automation system, controls, and manufacturing equipment issues
  • Provide hands-on troubleshooting support for production and maintenance teams
  • Perform system upgrades and maintenance to improve performance and reliability
Compliance & Validation
  • Ensure automation systems comply with FDA regulations, GMP standards, and industry best practices
  • Support validation activities and collaborate with Quality and regulatory teams on compliance-related issues
  • Apply knowledge of validation protocols and regulated manufacturing documentation requirements
Project & Technical Leadership
  • Support automation-related projects involving planning, design, reconfiguration, maintenance, and system improvements
  • Coordinate technical activities across stakeholders and site teams
  • Prepare project reports, performance metrics, and technical documentation
  • Train and support personnel on automation systems and related technologies
Basic Qualifications: Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience Preferred Qualifications:
  • Advanced degree in Mechatronics, Computer, Electrical, Mechanical, or Chemical Engineering
  • Experience supporting pharmaceutical or biotech manufacturing operations, particularly final drug product packaging
  • Strong background in manufacturing process controls, automation systems, field instrumentation, and lifecycle management
  • Experience with Rockwell/Allen-Bradley platforms; exposure to Siemens, Machine Vision, Serialization, or Robotics technologies
  • Knowledge of Data Integrity, GMPs, GAMP, and regulated manufacturing environments
  • Understanding of validation execution requirements and new equipment installation processes
  • Strong technical writing, communication, problem-solving, and project coordination skills
  • Knowledge of Operational Excellence and Lean manufacturing principles
Red Flags:
  • This is not primarily a Validation Engineer or Project Manager role
  • Candidates must have strong hands-on PLC troubleshooting and continuous improvement experience
Interview process: Virtual interview with manager. Virtual panel interview. We invite qualified candidates to send your resume to resumes@3keyconsulting.com.If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.

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