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Quality Control Analyst Jobs in Ohio (NOW HIRING)

Forge Biologics

Scientist I, QC Analytical

Columbus, OH · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Scientist I, Quality Control (Analytical) role will primarily focus on analytical method execution, method qualification, method validation, and troubleshooting efforts. This position will be ...

Forge Biologics

Scientist I, QC Analytical

Columbus, OH

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Scientist I, Quality Control (Analytical) role will primarily focus on analytical method execution, method qualification, method validation, and troubleshooting efforts. This position will be ...

PSG GROUP LLC

Quality Control QC Lead

Warren, OH · On-site

$28 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Relocation bonus Quality Control (QC) Lead $26.07 - $31.39 an hour - Temporary, Part-time, ... and trend analysis to project management. * Prepare final quality close-out documentation for ...

Merck Group

Quality Control Chemistry Team Lead

Miamisburg, OH · On-site

$64K - $107K/yr

  • Medical

  • Retirement

  • PTO

LS-SC-UOIQC Quality Control Analytics Recruiter: Michelle Cole This information is for internals only. Please do not share outside of the organization. Your Role The Quality Control Team Lead ...

Hycom, Inc.

Be Seen First

Quality Control Manager

Barberton, OH · On-site

$90K - $100K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

The QCM is responsible for all departmental activities and maintaining quality control processes, analyzing the results and giving feedback and guidance to the production team. S/he will develop ...

Jurgensen Companies

Quality Control Technician

Cincinnati, OH · On-site

$18 - $23/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Quality Control division provides our employees with a consistent path to learn and progress ... Analytical Thinking - Strong skills in data analysis, problem-solving, and interpretation of ...

Jurgensen Companies

Quality Control Technician

Cincinnati, OH · On-site

$18 - $23/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Quality Control division provides our employees with a consistent path to learn and progress ... Analytical Thinking - Strong skills in data analysis, problem-solving, and interpretation of ...

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Showing results 21-40

All JobsQuality Control Analyst JobsQuality Control Analyst Jobs in Ohio

Quality Control Analyst information

See Ohio salary details

$15

$26

$39

How much do quality control analyst jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality control analyst in Ohio is $26.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.92 and $29.47 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

What are the key skills and qualifications needed to thrive as a quality control analyst?

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by quality control analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What is a quality control analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

Is a quality control analyst a good job?

A quality control analyst is a valuable role in industries such as manufacturing, pharmaceuticals, and food production, focusing on ensuring products meet quality standards through testing and inspection. The job typically requires attention to detail, knowledge of testing tools and procedures, and may involve certifications like Six Sigma or ISO standards. It offers stable employment with opportunities for advancement and skill development.
More about Quality Control Analyst jobs

What are the most commonly searched types of Quality Control Analyst jobs in Ohio?

The most popular types of Quality Control Analyst jobs in Ohio are:

What are popular job titles related to Quality Control Analyst jobs in Ohio?

For Quality Control Analyst jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Quality Control Analyst jobs in Ohio look for?

The top searched job categories for Quality Control Analyst jobs in Ohio are:

What cities in Ohio are hiring for Quality Control Analyst jobs?

Cities in Ohio with the most Quality Control Analyst job openings:

What are popular job titles related to Quality Control Analyst jobs in OH?

For Quality Control Analyst jobs in OH, the most frequently searched job titles are:

Quality Control Analyst jobs near you
Infographic showing various Quality Control Analyst job openings in Ohio as of August 2026, with employment types broken down into 91% Full Time, and 9% Contract. Highlights an 100% In-person job distribution, with an average salary of $55,203 per year, or $26.5 per hour.

Scientist I, QC Analytical

Forge Biologics

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

Job description

Forge Your Future with Us:
At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities - all united by one goal: improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins.
Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen - you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases.
What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely, and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together.
At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us.
If you're ready to use your talent to help deliver hope to patients around the world, join us - and be part of something bigger than yourself.
About the Role:
The Scientist I, Quality Control (Analytical) role will primarily focus on analytical method execution, method qualification, method validation, and troubleshooting efforts. This position will be responsible for executing in-process, final product, and stability testing for AAV vectors, plasmids, and microbial and mammalian cell banks, while ensuring that activities occur in an efficient and cGMP compliant manner. This role will function as a subject matter expert (SME) for either nucleic acid-based methods (e.g. ddPCR, qPCR), protein-based assays (e.g. CE, AUC), or cell-based assays (e.g. TCID50, potency). This position will also be responsible for fostering innovation within the QC department, either independently or by partnering with Analytical Development, ensuring cutting edge technologies are employed to maintain the highest QC standards in the analysis of gene therapy products. This role provides an opportunity to play a significant impact in the success of client gene therapy programs.
Responsibilities:
  • Perform in-process, release, and stability testing for assays relevant to viral vector/gene therapy products, plasmids, and cell banks, including in-process testing, lot release testing, assay qualification, and validations.
  • Function as an SME for either nucleic acid-based methods (e.g. ddPCR, qPCR), protein-based assays (e.g. CE, AUC), or cell-based assays (e.g. TCID50, potency). Additionally, perform advanced analytical testing quality control assays, including compendial testing, ELISA, and viability assays, to assess the quality, potency, and safety of AAV vector products.
  • Support troubleshooting of processes/assays as an SME. Represent QC as a SME during audits and inspections.
  • Ensure effective qualifications, validations, and transfer of analytical methods to Quality Control in a phase-appropriate fashion, to support pre-clinical, clinical, and commercial activities.
  • Contribute to authoring and/or reviewing QC documentation, including but not limited to: SOPs, analytical methods and forms, qualifications protocols, and validation protocols.
  • Conducts thorough investigations to determine root cause of OOS investigations and other non-conforming results and implements appropriate corrective and preventative actions in a timely manner.
  • Provide support for Deviations, Change Controls, and CAPAs related to in process and final product testing.
  • Review and approve GMP documentation associated with in process, final product, and stability testing.
  • Drive the development, optimization, and validation of novel analytical methods to enhance quality control processes.
  • Provide technical guidance and mentorship to junior team members, promoting their personal growth and skill development.
  • Compile data with minimal oversight, generating reports, and archiving assay data; responsible for performing the analysis and interpretation of assay results.
  • Support regulatory and client inspections and internal audits of GMP systems.
  • Manage tracking and trending of in process and final product testing data, including, but not limited to; leading/participating in out of specification (OOS)/out of trend (OOT) Laboratory Investigations.

Qualifications:
  • Bachelor's, Master's, or PhD or in a relevant scientific field (e.g., biology, biochemistry, molecular biology). Advanced degree preferred.
  • SME for either nucleic acid-based methods (e.g. ddPCR, qPCR), protein-based assays (e.g. CE, AUC), or cell-based assays (e.g. TCID50, potency) based on experience. Advanced knowledge of complex molecular biology, biochemistry, or cell biology techniques and analytical methods (e.g., qPCR, cell-based infectivity assays, potency assays).
  • Proven ability to execute, troubleshoot, and optimize analytical assays.
  • Strong analytical and data interpretation skills to assess and drive quality improvement through the analysis of quality metrics and performance data.
  • Robust understanding of cGMP requirements as they pertain to Quality Control and Analytical Development testing.
  • Experience in leading, mentoring, and guiding junior team members.
  • Experience with electronic Quality Management Systems (EQMS), Laboratory Information Management Systems (LIMS), etc.

Work Environment and Physical Demands
This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area.
Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
We've Got You Covered:
At Forge Biologics, we believe our people deserve to be taken care of - in and out of the workplace. We've built a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way:
Health from day one
  • Health, dental and vision insurance start your first day - with 90% of premiums covered for you and your family.

Time to recharge
  • A competitive paid time off plan - because rest fuels innovation.
  • 12 weeks of fully paid parental leave so you can focus on family when it matters most.

Rewarding your impact
  • Annual bonus opportunities for all full-time team members.
  • 401(k) with company match to help you plan for the future.
  • Special employee discounts, including childcare and dependent care savings.

Your wellness, supported
  • Onsite fitness facility at The Hearth.
  • Mental health counseling and financial planning services through our Employee Assistance Program.
  • Employer-paid short and long-term disability coverage to protect your peace of mind.

Fuel for your workday
  • A fully stocked kitchen with free snacks and beverages - we keep you energized and ready for what's next.

Grow with us
  • Ongoing professional development resources, training, and mentorship programs to help you build your care and grow within Forge.

Apply