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Biotech Manufacturing Jobs in Ohio (NOW HIRING)

Pinnaql

Jr Validation Engineer

New Albany, OH

... biotech manufacturing site. The role supports validation documentation and execution activities in a regulated GMP environment. Key Responsibilities * Support preparation, execution, and review of ...

Pinnaql

Jr Validation Engineer

New Albany, OH · On-site

... biotech manufacturing site. The role supports validation documentation and execution activities in a regulated GMP environment. Key Responsibilities * Support preparation, execution, and review of ...

Amgen

Manager Manufacturing (12hr PM)

New Albany, OH · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Manager, Manufacturing- 12 Hour PM (6:00pm - 6:30am) What you will do Let's do this. Let's change ...

Zifo

GxP Lab Computing Analyst

Beachwood, OH · On-site

Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team ...

Zifo

GxP Lab Computing Analyst

Beachwood, OH · On-site

Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team ...

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All JobsBiotech Manufacturing JobsBiotech Manufacturing Jobs in Ohio

Biotech Manufacturing information

See Ohio salary details

$11

$19

$31

How much do biotech manufacturing jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for biotech manufacturing 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 is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

What are the key skills and qualifications needed to thrive in biotech manufacturing?

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

How to get into biotech manufacturing?

To enter biotech manufacturing, candidates typically need a background in biology, chemistry, or related fields, often requiring a bachelor's degree or higher. Gaining experience through internships or entry-level positions, developing skills in laboratory techniques and GMP (Good Manufacturing Practice), and obtaining certifications such as cGMP training can improve job prospects. Familiarity with manufacturing equipment and attention to quality control are also important for success in this field.

What are the most commonly searched types of Biotech Manufacturing jobs in Ohio?

The most popular types of Biotech Manufacturing jobs in Ohio are:

What are popular job titles related to Biotech Manufacturing jobs in Ohio?

For Biotech Manufacturing jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Biotech Manufacturing jobs in Ohio look for?

The top searched job categories for Biotech Manufacturing jobs in Ohio are:

What cities in Ohio are hiring for Biotech Manufacturing jobs?

Cities in Ohio with the most Biotech Manufacturing job openings:

Biotech Manufacturing jobs near you
Infographic showing various Biotech Manufacturing job openings in Ohio as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, 6% Contract, and 2% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $41,204 per year, or $19.8 per hour.

Commissioning & Qualification Engineer, Jr. - New Albany, Ohio

Ultimate Solutions

New Albany, OH • On-site

Full-time

Re-posted 10 days ago

Job description

Commissioning & Qualification Engineer, Jr.
At Ultimate Solutions, we deliver engineering, automation, serialization, and compliance solutions to the world's leading pharmaceutical, biotechnology, medical device, and logistics companies.
For more than 20 years, our team has successfully supported complex manufacturing and packaging projects across Puerto Rico, the United States, and Europe. We are known for delivering high-impact technical solutions, strong client partnerships, and exceptional project execution in highly regulated industries.
We are currently seeking a motivated and hands-on Commissioning & Qualification (C&Q) Engineer, Jr. to support exciting biotech manufacturing startup and expansion projects in New Albany.
This is an excellent opportunity for engineers with solid GMP experience who want to grow their careers while working alongside experienced industry leaders in a fast-paced and highly technical environment.
What You'll Do
  • Support commissioning and qualification activities for process equipment, utilities, facilities, packaging systems, and automation platforms.
  • Execute and document IQ, OQ, and PQ protocols in compliance with GMP and regulatory requirements.
  • Assist with startup, troubleshooting, testing, and system turnover activities.
  • Develop and review C&Q documentation including protocols, reports, test scripts, and traceability matrices.
  • Verify systems meet design specifications, user requirements, and operational expectations.
  • Collaborate with engineering, automation, validation, manufacturing, and quality teams to meet project milestones.
  • Support deviation investigations, change controls, and CAPA activities.
  • Maintain accurate, audit-ready documentation throughout project execution.
  • Travel to OEM/vendor facilities to support and execute Factory Acceptance Testing (FAT) and validation activities prior to equipment shipment and site installation.
  • Promote safe work practices and compliance with environmental and quality standards.

What We're Looking For
  • Bachelor's degree in Engineering, Life Sciences, or a related technical field.
  • Minimum of 2 years of solid experience in Commissioning, Qualification, Validation, or related GMP-regulated activities.
  • Experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Working knowledge of IQ/OQ/PQ methodologies, GMP regulations, and industry standards.
  • Ability to read and interpret P&IDs, engineering drawings, and technical documentation.
  • Strong technical writing, organizational, and problem-solving skills.
  • Team-oriented mindset with excellent communication skills.
  • Ability and willingness to travel to OEM/vendor facilities for FAT execution and project support.
  • Willingness to work in a dynamic, schedule-driven project environment.

Preferred Qualifications
  • Experience supporting biotech or pharmaceutical startup projects.
  • Familiarity with ISPE Baseline Guides and ASTM E2500.
  • Exposure to automation systems, utilities, or process equipment qualification.
  • Knowledge of risk-based C&Q methodologies.
  • Experience supporting deviations, investigations, and change control processes.

Why Join Ultimate Solutions?
  • Work on cutting-edge biotech manufacturing projects.
  • Join a collaborative and highly technical engineering team.
  • Career growth opportunities within a global engineering organization.
  • Exposure to large-scale GMP startup and expansion projects.
  • Competitive compensation and professional development opportunities.

Not open for Corp-to-Corp arrangements
Equal Opportunity Employer
Ultimate Solutions is an Equal Opportunity Employer. We are committed to creating an inclusive workplace where all employees and applicants are treated with respect and provided equal employment opportunities regardless of race, color, religion, sex, national origin, disability, veteran status, or any other protected characteristic under applicable law.

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