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Biotech Quality Control Jobs in Ohio (NOW HIRING)

Centor

Quality Lab Technician PPP NA

Millersburg, OH · On-site

$24.35/hr

... pharma, biotech and cosmetic industries. The company offers a comprehensive portfolio of ... Area of responsibility Quality Control: * Perform visual and dimensional inspections (microscope ...

Actalent

Document Control Specialist

Bedford, OH

$21 - $22/hr

Associate's or Bachelor's degree in Biology, Chemistry, Biotechnology, or related field. * Experience in laboratory settings, QA/QC, R&D, or similar scientific environments is preferred. * Ability to ...

PSC Biotech

Validation Engineer

Columbus, OH

Partner with Engineering, Quality, IT, and external vendors to ensure systems are implemented and ... pharma, biotech) Well-versed in manufacturing systems, including automation platforms, control ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Ohio

Biotech Quality Control information

See Ohio salary details

$29K

$77.3K

$123.1K

How much do biotech quality control jobs pay per year?

As of Jul 26, 2026, the average yearly pay for biotech quality control in Ohio is $77,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $95,100.00 per year, depending on experience, location, and employer.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
What are the most commonly searched types of Biotech Quality Control jobs in Ohio? The most popular types of Biotech Quality Control jobs in Ohio are:
What are popular job titles related to Biotech Quality Control jobs in Ohio? For Biotech Quality Control jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Ohio look for? The top searched job categories for Biotech Quality Control jobs in Ohio are:
What cities in Ohio are hiring for Biotech Quality Control jobs? Cities in Ohio with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Ohio as of July 2026, with employment types broken down into 90% Full Time, 3% Part Time, 1% Temporary, and 6% Contract. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution, with an average salary of $77,314 per year, or $37.2 per hour.
QC Systems Engineer IV (LabVantage LIMS)

QC Systems Engineer IV (LabVantage LIMS)

Resilience

West Chester, OH • On-site

Full-time

Posted 10 days ago

Job description

Job Summary:
Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. The Quality Control Systems Engineer will act as a senior technical contributor and delivery lead for LabVantage LIMS/LES, ensuring the reliable, compliant operation of critical laboratory applications and data acquisition systems.
Responsibilities:
• Serve as senior LabVantage technical subject matter expert for project execution and system enhancements, responsible for configuration, deployment, validation, adoption, and troubleshooting of LabVantage modules.
• Lead and manage enhancement projects to expand or upgrade QC applications, including rollouts of new LabVantage modules and development of reports and labels.
• Partner with scientific business stakeholders (e.g., QC) to gather and document user requirements and create actionable application designs and implementation plans.
• Provide troubleshooting and guidance for LabVantage issues and complex configurations.
• Support system integrations and assist in architecting solutions to enable secure and reliable data flow across applications.
• Serve as system support for QC applications, managing user accounts, access rights, roles, and privileges. Ensure reliable, compliant operation of critical QC systems.
• Manage change controls, deviations, and related records in the electronic Quality Management System (eQMS) for QC system projects. Partner with Quality and CSV to ensure regulatory compliance.
• Own and execute GxP validation activities for projects and system enhancements. Develop and maintain validation and system lifecycle documentation (e.g., SRS, specifications, IQ/OQ/PQ testing, SOPs).
• Maintain compliance and audit readiness of assigned systems, ensuring adherence to 21 CFR Part 11 and other regulatory standards.
Qualifications:
Required:
• Experience developing and maintaining LabVantage reports preferably using Jaspersoft Studio.
• Extensive experience maintaining LabVantage LIMS in biotech, pharma, or life sciences.
• Experience developing and maintaining label printing solutions, preferably in BarTender.
• Strong project leadership experience, including planning and managing multiple concurrent projects.
• Excellent communication skills, with the ability to translate technical concepts for non-technical stakeholders.
• Strong analytical and problem-solving skills, with the ability to independently diagnose and resolve complex system issues.
• Programming experience using SQL.
• Experience with LabVantage architecture, including JBOSS, Microsoft SQL Server, and/or Apache or other applicable program.
• Experience with GxP validation and understanding of regulatory requirements (e.g., GxP, 21 CFR Part 11).
• Proven experience authoring and maintaining SOPs, validation protocols, and system lifecycle documents.
Preferred:
• Bachelor’s degree in a scientific, technical, or related discipline.
• 5+ years of experience maintaining LabVantage LIMS in biotech, pharma, or life sciences.
• Experience with system lifecycle management, including upgrades, patches, and periodic reviews.
• Experience with Empower, Moda, Novatek, or other data acquisition systems.
• Experience implementing and supporting LabVantage Work Assignment and Planning module.
• Programming experience using JavaScript and/or Groovy.
• Familiarity with electronic Quality Management Systems (eQMS), such as Veeva.
• Experience designing and supporting integrations with enterprise systems (e.g., ERP, data platforms).
Company:
Resilience is a biomanufacturing company that provides access to complex medicines and protects biopharmaceutical supply chains. Founded in 2020, the company is headquartered in La Jolla, USA, with a team of 1001-5000 employees. The company is currently Late Stage.

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