64 QA Engineering Jobs in Columbus, OH, United States

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• The Quality Engineer contributes to risk management, design controls, manufacturing and supplier quality, data-driven problem solving, and…
• Partner with manufacturing teams to resolve quality issues, support incoming inspection processes and sampling plan execution, and particip…

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• Job Summary Battelle is seeking a Principal Quality Engineer to serve as the enterprise technical authority for nuclear Quality Assurance…
• The Principal Quality Engineer acts as a trusted advisor to senior leadership, customers, and regulators, shaping quality strategy, regulat…

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• The QE partners closely with Manufacturing and Engineering to stabilize processes and prevent recurrence of quality issues.
• Routine inspection and testing are primarily executed by the Quality Technician role; the QE provides technical support and escalation cove…

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• Monitor and report on process performance and effectiveness metrics (e.g., Process Effectiveness Index, audit results, defect trends) Suppo…
• Preferred Qualifications: Certified Quality Engineer or equivalent certification.

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• The External Supply QRO Specialist is expected to own and execute independently all the processes related to Raw Material and…
• This Specialist Manufacturing will act as the External Supply QRO representative across functional teams and external suppliers to drive cl…

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• The Opportunity Our location in Columbus, OH currently has an opportunity for a Manager Quality Assurance - US Distribution Quality…

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• The Specialist I, QA Operations is responsible for ensuring compliance with regulatory requirements and maintaining the highest quality sta…
• Preferred Skills: Direct experience in providing QA support for cGMP manufacturing operations in a cleanroom environment .

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• Technical leadership of external manufacturing partners under regulated quality requirements.
• External Manufacturing Act as senior packaging technical authority for the third-party manufacturing network with documentation, process co…

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• Experienced developing Packaging PFMEA and DFMEA.
• Skilled in verification and validation of content sterile packaging systems, ensuring compliance with regulatory standards.

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• Job Summary The quality assurance specialist (QAS) performs all quality review and approval/release decisions at an FDA-regulated drug manu…
• Engages and collaborates with operations department to drive quality system and CGMP requirements.

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• Responsible for leading assigned Quality Lab commercial product flows as well as product lifecycle and continuous improvement efforts.

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• Collaborate with cross-functional teams, including Quality Assurance (QA) and Quality Control (QC), to investigate and resolve deviations,…
• Preferred Skills: Prior experience working in a cGMP manufacturing environment.

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• Provide technical/engineering support and design authority for fielded products.
• This role provides post-launch technical product support, including evaluation and approval of engineering and artwork changes, configurati…

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• Job Summary To support our mission, the Health Research and Analytics (HRA) business line is currently seeking a Senior Quality…
• Key Qualifications 5+ years of experience developing or endorsing clinical quality measures 5+ years working on Centers for Medicare &…

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• Technical Responsibilities - Develop documentation for CQV activities - Write and execute protocols (field verification) - Develop summary…
• For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated op…

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• Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their…
• Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to…

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• Compliance Engineering experience Excellent communication skills, both written and verbal.
• Guides the tasks of shared-resource R&D compliance engineers.

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• Come join us as a Quality Systems (Veeva) Senior Consultant, and in this role, you will deliver creative business solutions…
• What You’ll Do As a Quality Systems (Veeva) Senior Consultant at Clarkston, you will: Participate in projects at life sciences…

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• Aseptic Processing & Sterile Manufacturing Provide technical leadership for aseptic processing and sterile manufacturing systems, including…
• The Product Launch & Lifecycle Engineer will manage cross-functional project teams to support product launch, lifecycle, and technical tran…

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• This role involves executing reactive, preventive, and predictive maintenance, troubleshooting mechanical, hydraulic, pneumatic, and contro…
• Proficiency in troubleshooting PLCs, HMIs, and automated systems.

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• Experience with MasterControl or other electronic quality management system preferred.
• Manager, Regulatory Affairs & Stability, the Quality Control Lab Manager is responsible for the management of the AHP Quality Control…

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• This position is responsible for strengthening the Quality Management System (QMS) , improving product and process quality, maintaining com…
• Effective QMS, process controls, and compliance.

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• Ability to learn clean room technology and use of aseptic technique.
• Conducts all water samplings throughout manufacturing facility.

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• This position will work under the direction of the Quality Systems Supervisor or Manager.
• Audits and maintains records for non-batch log related items (i.e.: Tank Temps, CIP charts) Identifies and communicates withmanufacturing p…

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• This position provides hands-on leadership, daily project interface, and real-time quality risk management for active fabrication shops and…
• Other duties as assigned by the Director of QA/QC in conjunction with the project team.