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Gmp Manufacturing Jobs in Ohio (NOW HIRING)

Actalent

GMP Scientist I

Columbus, OH

$24/hr

This role focuses on hands-on cell-based manufacturing in a GMP setting, not research, and involves executing production processes, maintaining accurate documentation, and supporting facility and ...

Akraya Inc.

Device Engineer

New Albany, OH · On-site

$30 - $33/hr

Instron Systems (intermediate), Force tester (intermediate), Optical Measurement (beginner), Technical Documentation (advanced), GMP Manufacturing (advanced), Microsoft Office (advanced), CAD ...

Actalent

GMP Scientist II (Suspension)

Columbus, OH

$28/hr

Provide leadership in daily operational activities related to GMP manufacturing of biological products. * Ensure availability of materials and proper documentation of GMP activities and product ...

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How much do gmp manufacturing jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for gmp manufacturing in Ohio is $23.72, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $27.40 per hour, depending on experience, location, and employer.

What is a GMP manufacturing?

A GMP Manufacturing job involves producing pharmaceutical, biotechnology, or medical device products while following Good Manufacturing Practices (GMP) regulations. Responsibilities typically include operating equipment, maintaining sterile environments, documenting processes, and ensuring product quality and compliance. These roles are essential for maintaining safety and regulatory standards in healthcare-related manufacturing industries.

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

To excel in GMP Manufacturing, you need a solid understanding of Good Manufacturing Practices, attention to detail, and experience in regulated production environments, often backed by a degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and equipment such as bioreactors or chromatography columns is typically required, and certifications like GMP or Six Sigma can be beneficial. Strong teamwork, communication skills, and the ability to follow precise procedures are essential soft skills for this position. These competencies ensure safe, compliant, and efficient production of pharmaceuticals or biotechnology products within strict regulatory frameworks.

What are some common challenges faced in GMP manufacturing roles?

Employees in GMP Manufacturing often encounter challenges such as maintaining meticulous documentation, adapting to changing regulatory requirements, and adhering to strict cleanliness and safety standards. The production process must be tightly controlled and deviations must be reported and resolved promptly, which requires a high level of diligence and accountability. Additionally, working collaboratively with quality assurance, engineering, and other cross-functional teams can add complexity to daily operations. Overcoming these challenges helps ensure product quality and regulatory compliance, while also providing valuable professional experience in one of the most highly regulated industries.

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

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

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

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

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

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

What cities in Ohio are hiring for Gmp Manufacturing jobs?

Cities in Ohio with the most Gmp Manufacturing job openings:

Gmp Manufacturing jobs near you
Infographic showing various Gmp Manufacturing job openings in Ohio as of August 2026, with employment types broken down into 84% Full Time, 8% Contract, and 8% Nights. Highlights an 100% In-person job distribution, with an average salary of $49,331 per year, or $23.7 per hour.

Device Engineer - GMP Manufacturing Support & Mechanical Testing (JP15754)

New Albany, OH

3 Key Consulting
Biotechnology Research and Development • 1 - 10 employees
Learn more about 3 Key Consultingexternal

$31 - $35/hr

Full-time

Posted 6 days ago

Job description

Job Title:   Device Engineer – GMP Manufacturing Support & Mechanical Testing (JP15754)
Location: New Albany, OH 43054
Employment Type: Contract
Business Unit: Commercial Drug Product
Duration: 1+ year (with likely extensions and/or conversion to permanent)
Posting Date: 08/20/2026
Pay Rate: $31 - $35/hour W2
Notes: Only qualified candidates need apply.  Fully Onsite (5 Days per Week) standard hours.  Potential overtime.
3 Key Consulting is hiring a  Device Engineer – GMP Manufacturing Support & Mechanical Testing for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Our ideal candidate:
  • Hands-on experience in engineering environments, particularly with tools like Instron systems and optical measurement methods
  • Proficiency in technical documentation and teamwork.
  • Hands-on experience working within a GMP manufacturing environment is required, including familiarity with GMP documentation practices, manufacturing operations, and quality systems.
  • Experience in regulated industries, preferably biopharma, biomedical, or medical devices, is strongly preferred, though aerospace or mechanical disciplines are acceptable provided the candidate also has relevant GMP manufacturing experience.
  • Proficiency in Microsoft Office is required, and CAD/SolidWorks skills are a plus.
  • Entry-level candidates with practical experience, such as internships within a GMP manufacturing or similarly regulated production environment, are preferred.

The Device Engineer will provide technical engineering support for material and component-related issues associated with commercial drug delivery devices and manufacturing operations. The primary focus of this role will be the triage, testing, investigation, escalation, and documentation of material-related issues identified during manufacturing or through other quality and technical support processes.
The engineer will work closely with Manufacturing, Quality, Engineering, and other cross-functional partners to assess reported issues, determine appropriate testing and investigation strategies, generate and review technical data, and support timely disposition or escalation of issues.
Scope includes mechanical delivery devices and associated components, including prefilled syringe systems. The qualified candidate will be part of a sustaining device engineering team supporting commercial manufacturing and product lifecycle activities. This position requires strong attention to detail, hands-on technical capabilities, and the ability to accurately document work within a GMP-regulated environment.
Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
  • Strong Communication
  • Experience in a GMP Manufacturing Environment
  • Strong Technical Writing
  • Soft skills that need to be screened for: Looking for a self starter, someone who is ambitious

Day to Day Responsibilities:
  • Collaborate Cross-Functionally with the Various SMEs at the FDP Manufacturing Sites to Identify Device Issues and Root Causes
  • Expanding Documentation of Site Capability and Control Strategies
  • Ensuring Expedited communication to wider team on risks to device manufacturing
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Maintains combination product design history files for assigned products
  • Develops characterization test methods through fixture prototyping, reference sample creation, and GR&R analysis
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
  • Individual contributor with Leadership attributes to effectively represent device engineer within a large network/matrix organization

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
  • At a minimum familiar with the following standards and regulations:
    • Quality System Regulation – 21CFR820
    • Risk Management – ISO 14971
    • EU Medical Device requirements – Council Directive 93/42/EEC
  • Demonstrates experience working in a GMP manufacturing environment and adheres to strict GMP documentation and compliance practices
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.

Preferred Qualifications:
  • Bachelor’s Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Minimum 2 years of scientific or engineering experience working in a GMP regulated manufacturing environment
  • Demonstrated understanding of GMP manufacturing operations, documentation practices, deviations/change controls, and working within an established quality system
  • Statistical Analysis software (Minitab or JMP)
  • Strong technical writing skills
  • CAD fixturing software (SolidWorks)
  • Tolerance Stack-Ups (2D, 3D, RSS)
  • Instron force tester using BlueHill Universal
  • CT-Scanning
  • Deviations and CAPAs
  • Experience with design controls; including (but not limited to) verification and design transfer
  • Understanding of risk assessments including hazard and probability analysis
  • Background in medical device development, commercialization and knowledge of manufacturing processes (fill-finish)
  • Ability to work independently and dynamically across functional teams
  • Excellent written and verbal communication skills
  • Ability to support complex workstreams under demanding timelines

Employee Value Proposition:
Unique industry opportunity, industry experience
Red Flags:
  • No Cross-Functional Experience
  • No Practical Work Experience

Interview process:
Initial 1:1 Phone Interview with Hiring Manager
Group Interview with CORE SMEs
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.