QA Engineer Jobs in Columbus, OH
QA Engineer jobs in Columbus are actively hiring across the Short North tech corridor, Dublin's enterprise software cluster, and the Easton and New Albany business parks, with strong demand in fintech, healthcare IT, and e-commerce. Employers hiring right now include Lower, Revel IT, and Handgards. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 17+ QA Engineer jobs
Position Summary:
The Quality Assurance Technician I supports Quality Assurance operations within a 503B pharmaceutical manufacturing environment by helping ensure products, processes, documentation, materials, and labeling activities meet cGMP, company procedure, and quality system expectations. This role provides day-to-day QA support across Production, Warehouse, Receiving, and Quality while helping protect patient safety through accurate inspection, documentation, escalation, and follow-up.
This position is a strong fit for someone who is detail-oriented, organized, comfortable working in a regulated manufacturing environment, and motivated to grow within pharmaceutical Quality Assurance. The QA Technician I may support a mix of floor-based quality checks and documentation-based activities, including sampling and inspection, labeling coordination, GMP document review, QMS support, training/document control support, and follow-up on quality events or process concerns.
What This Role Does Day-to-Day:
In this role, the QA Technician I helps verify that work performed in manufacturing and support areas is completed accurately, consistently, and in accordance with approved procedures. Daily activities may include sampling or inspecting in-process and finished products, verifying label or component information, reviewing room and equipment logs, reviewing master batch production records or related GMP documentation, entering quality data, supporting metric and trend tracking, and assisting with quality system records.
The QA Technician I may also support investigations, CAPAs, effectiveness checks, customer complaint follow-up, supplier-related activities, receiving inspection support, and document control or training program activities. The role requires the ability to recognize when something does not match the procedure, documentation, label, material, product, or expected process, and to escalate the concern before moving forward.
Because this position supports multiple departments, the ideal candidate must be comfortable communicating with Production, Warehouse, Receiving, Quality Control, Quality Assurance, and leadership. Success in this role requires strong attention to detail, sound judgment, professionalism, follow-through, and the ability to balance urgency with compliance in a fast-paced manufacturing environment.
Key Responsibilities:
- Perform sampling and inspection of in-process and finished pharmaceutical products according to approved procedures, specifications, and quality expectations.
- Support and facilitate finished product labeling activities, including label coordination, verification, reconciliation support, documentation, and escalation of labeling discrepancies as assigned.
- Review GMP documentation, including master batch production records, room logs, equipment logs, inspection records, forms, checklists, and other quality-related documents for accuracy, completeness, and compliance.
- Support manufacturing and receiving activities by verifying materials, components, documentation, supplier-related information, or inspection requirements as assigned.
- Assist with investigations related to deviations, documentation discrepancies, process concerns, product issues, supplier concerns, label discrepancies, complaints, or other quality events.
- Support corrective and preventive action activities, including fact gathering, follow-up, implementation support, and effectiveness checks.
- Support quality management system activities, including document control, training program management, record review, quality data entry, metrics, and trending.
- Identify and escalate potential deviations, documentation errors, missing information, product defects, material concerns, label mismatches, or process issues to the appropriate Quality or operational leader.
- Work cross-functionally with Production, Warehouse, Receiving, QC, QA, and leadership to support compliant operations, timely issue resolution, and product quality.
- Maintain accurate, timely, legible, complete, and attributable documentation in accordance with GDP expectations.
- Follow all applicable cGMP, GDP, FDA, OSHA, DEA, company procedure, safety, PPE, and quality system requirements.
- Support continuous improvement by identifying recurring issues, communicating improvement opportunities, and participating in process or quality system improvements.
- Perform other duties as assigned based on business and quality needs.
What Success Looks Like:
- Understands that QA support directly impacts patient safety, product quality, product release, and regulatory compliance.
- Reviews documentation carefully and catches missing, inconsistent, incomplete, or inaccurate information before it creates a larger issue.
- Identifies product, material, label, documentation, or process concerns and escalates appropriately instead of making assumptions or unsupported decisions.
- Maintains objectivity, professionalism, and confidentiality when supporting investigations, CAPAs, complaints, or quality events.
- Communicates clearly with Production, Warehouse, Receiving, QC, QA, and leadership, especially when priorities shift or concerns need follow-up.
- Stays organized while managing multiple tasks, open items, deadlines, and documentation requirements.
- Follows SOPs and work instructions exactly and understands the importance of cGMP, GDP, and data integrity.
- Demonstrates accountability, curiosity, and willingness to learn broader quality systems and pharmaceutical manufacturing processes.
- Shows motivation to grow within Quality Assurance and take on additional QMS, investigation, documentation, or floor support responsibilities over time.
Required Qualifications:
- Understands that QA support directly impacts patient safety, product quality, product release, and regulatory compliance.
- Reviews documentation carefully and catches missing, inconsistent, incomplete, or inaccurate information before it creates a larger issue.
- Identifies product, material, label, documentation, or process concerns and escalates appropriately instead of making assumptions or unsupported decisions.
- Maintains objectivity, professionalism, and confidentiality when supporting investigations, CAPAs, complaints, or quality events.
- Communicates clearly with Production, Warehouse, Receiving, QC, QA, and leadership, especially when priorities shift or concerns need follow-up.
- Stays organized while managing multiple tasks, open items, deadlines, and documentation requirements.
- Follows SOPs and work instructions exactly and understands the importance of cGMP, GDP, and data integrity.
- Demonstrates accountability, curiosity, and willingness to learn broader quality systems and pharmaceutical manufacturing processes.
- Shows motivation to grow within Quality Assurance and take on additional QMS, investigation, documentation, or floor support responsibilities over time.
Physical Requirements:
- Ability to sit, stand, walk, bend, reach, or perform computer-based work for extended periods as required by business needs.
- Ability to lift up to 50 pounds at times.
- Ability to work in office, manufacturing, warehouse, receiving, controlled, or quality support areas as needed.
- Ability to wear required PPE and follow safety, cleanliness, gowning, and facility requirements.
- Ability to review documentation, labels, product information, and computer-based records for extended periods
Work Environment:
This role supports Quality Assurance activities in a 503B pharmaceutical manufacturing environment. Work may take place in office, production, warehouse, receiving, controlled, or other quality support areas. Employees are expected to follow cGMP, GDP, PPE, safety, documentation, cleanliness, and conduct expectations at all times. The role may involve working near production materials, finished products, labels, packaging components, equipment, or manufacturing documentation that must be handled according to approved procedures.
This is a quality-focused role where accuracy, consistency, escalation, and documentation matter. The QA Technician I helps ensure that issues are identified early, records are complete and accurate, and operational teams have the QA support needed to maintain compliant manufacturing and product quality.
Benefits:
We offer a comprehensive and competitive benefits package designed to support the health, well-being, and financial security of our employees and their families.
At STAQ Pharma, all full time employees have access to:
- Medical, dental, and vision insurance options
- Employer-paid life insurance and disability coverage
- Employee Assistance Program
- 401(k) retirement plan with employer match
- Paid time off (PTO), sick leave
- 7 paid holidays
- Opportunities for professional growth in a regulated pharmaceutical manufacturing environment
- Employee-focused culture emphasizing safety, quality, and teamwork
The application window for this position is anticipated to be open at least 25 days
Position Summary:
The Quality Assurance Technician I supports Quality Assurance operations within a 503B pharmaceutical manufacturing environment by helping ensure products, processes, documentation, materials, and labeling activities meet cGMP, company procedure, and quality system expectations. This role provides day-to-day QA support across Production, Warehouse, Receiving, and Quality while helping protect patient safety through accurate inspection, documentation, escalation, and follow-up.
This position is a strong fit for someone who is detail-oriented, organized, comfortable working in a regulated manufacturing environment, and motivated to grow within pharmaceutical Quality Assurance. The QA Technician I may support a mix of floor-based quality checks and documentation-based activities, including sampling and inspection, labeling coordination, GMP document review, QMS support, training/document control support, and follow-up on quality events or process concerns.
What This Role Does Day-to-Day:
In this role, the QA Technician I helps verify that work performed in manufacturing and support areas is completed accurately, consistently, and in accordance with approved procedures. Daily activities may include sampling or inspecting in-process and finished products, verifying label or component information, reviewing room and equipment logs, reviewing master batch production records or related GMP documentation, entering quality data, supporting metric and trend tracking, and assisting with quality system records.
The QA Technician I may also support investigations, CAPAs, effectiveness checks, customer complaint follow-up, supplier-related activities, receiving inspection support, and document control or training program activities. The role requires the ability to recognize when something does not match the procedure, documentation, label, material, product, or expected process, and to escalate the concern before moving forward.
Because this position supports multiple departments, the ideal candidate must be comfortable communicating with Production, Warehouse, Receiving, Quality Control, Quality Assurance, and leadership. Success in this role requires strong attention to detail, sound judgment, professionalism, follow-through, and the ability to balance urgency with compliance in a fast-paced manufacturing environment.
Key Responsibilities:
- Perform sampling and inspection of in-process and finished pharmaceutical products according to approved procedures, specifications, and quality expectations.
- Support and facilitate finished product labeling activities, including label coordination, verification, reconciliation support, documentation, and escalation of labeling discrepancies as assigned.
- Review GMP documentation, including master batch production records, room logs, equipment logs, inspection records, forms, checklists, and other quality-related documents for accuracy, completeness, and compliance.
- Support manufacturing and receiving activities by verifying materials, components, documentation, supplier-related information, or inspection requirements as assigned.
- Assist with investigations related to deviations, documentation discrepancies, process concerns, product issues, supplier concerns, label discrepancies, complaints, or other quality events.
- Support corrective and preventive action activities, including fact gathering, follow-up, implementation support, and effectiveness checks.
- Support quality management system activities, including document control, training program management, record review, quality data entry, metrics, and trending.
- Identify and escalate potential deviations, documentation errors, missing information, product defects, material concerns, label mismatches, or process issues to the appropriate Quality or operational leader.
- Work cross-functionally with Production, Warehouse, Receiving, QC, QA, and leadership to support compliant operations, timely issue resolution, and product quality.
- Maintain accurate, timely, legible, complete, and attributable documentation in accordance with GDP expectations.
- Follow all applicable cGMP, GDP, FDA, OSHA, DEA, company procedure, safety, PPE, and quality system requirements.
- Support continuous improvement by identifying recurring issues, communicating improvement opportunities, and participating in process or quality system improvements.
- Perform other duties as assigned based on business and quality needs.
What Success Looks Like:
- Understands that QA support directly impacts patient safety, product quality, product release, and regulatory compliance.
- Reviews documentation carefully and catches missing, inconsistent, incomplete, or inaccurate information before it creates a larger issue.
- Identifies product, material, label, documentation, or process concerns and escalates appropriately instead of making assumptions or unsupported decisions.
- Maintains objectivity, professionalism, and confidentiality when supporting investigations, CAPAs, complaints, or quality events.
- Communicates clearly with Production, Warehouse, Receiving, QC, QA, and leadership, especially when priorities shift or concerns need follow-up.
- Stays organized while managing multiple tasks, open items, deadlines, and documentation requirements.
- Follows SOPs and work instructions exactly and understands the importance of cGMP, GDP, and data integrity.
- Demonstrates accountability, curiosity, and willingness to learn broader quality systems and pharmaceutical manufacturing processes.
- Shows motivation to grow within Quality Assurance and take on additional QMS, investigation, documentation, or floor support responsibilities over time.
Required Qualifications:
- Understands that QA support directly impacts patient safety, product quality, product release, and regulatory compliance.
- Reviews documentation carefully and catches missing, inconsistent, incomplete, or inaccurate information before it creates a larger issue.
- Identifies product, material, label, documentation, or process concerns and escalates appropriately instead of making assumptions or unsupported decisions.
- Maintains objectivity, professionalism, and confidentiality when supporting investigations, CAPAs, complaints, or quality events.
- Communicates clearly with Production, Warehouse, Receiving, QC, QA, and leadership, especially when priorities shift or concerns need follow-up.
- Stays organized while managing multiple tasks, open items, deadlines, and documentation requirements.
- Follows SOPs and work instructions exactly and understands the importance of cGMP, GDP, and data integrity.
- Demonstrates accountability, curiosity, and willingness to learn broader quality systems and pharmaceutical manufacturing processes.
- Shows motivation to grow within Quality Assurance and take on additional QMS, investigation, documentation, or floor support responsibilities over time.
Physical Requirements:
- Ability to sit, stand, walk, bend, reach, or perform computer-based work for extended periods as required by business needs.
- Ability to lift up to 50 pounds at times.
- Ability to work in office, manufacturing, warehouse, receiving, controlled, or quality support areas as needed.
- Ability to wear required PPE and follow safety, cleanliness, gowning, and facility requirements.
- Ability to review documentation, labels, product information, and computer-based records for extended periods
Work Environment:
This role supports Quality Assurance activities in a 503B pharmaceutical manufacturing environment. Work may take place in office, production, warehouse, receiving, controlled, or other quality support areas. Employees are expected to follow cGMP, GDP, PPE, safety, documentation, cleanliness, and conduct expectations at all times. The role may involve working near production materials, finished products, labels, packaging components, equipment, or manufacturing documentation that must be handled according to approved procedures.
This is a quality-focused role where accuracy, consistency, escalation, and documentation matter. The QA Technician I helps ensure that issues are identified early, records are complete and accurate, and operational teams have the QA support needed to maintain compliant manufacturing and product quality.
Benefits:
We offer a comprehensive and competitive benefits package designed to support the health, well-being, and financial security of our employees and their families.
At STAQ Pharma, all full time employees have access to:
- Medical, dental, and vision insurance options
- Employer-paid life insurance and disability coverage
- Employee Assistance Program
- 401(k) retirement plan with employer match
- Paid time off (PTO), sick leave
- 7 paid holidays
- Opportunities for professional growth in a regulated pharmaceutical manufacturing environment
- Employee-focused culture emphasizing safety, quality, and teamwork
The application window for this position is anticipated to be open at least 25 days
See All 17 QA Engineer Jobs in Columbus
Find roles in Columbus that match your experience and apply in just a few clicks.
Find QA Engineer JobsQA Engineer Job Market in Columbus
Who's Hiring
Top Industries Hiring
- Banking & Financial Services
- Fintech
- Education
- Technology & Software
- Construction & Real Estate
QA Engineer Jobs in Columbus: Frequently Asked Questions
How do I get a qa engineer job in Columbus?
Focus your search on Columbus's core hiring sectors: fintech companies concentrated downtown and in Dublin, healthcare IT firms near the medical campus and Easton, and e-commerce and retail tech operations in New Albany. Candidates who can demonstrate experience with test automation frameworks and agile workflows stand out in this market. Tailoring your resume to the specific tech stack each employer uses gives you a concrete edge over generalist applicants.
Which companies hire qa engineers in Columbus?
Employers hiring qa engineers in Columbus right now include Lower, Revel IT, and Handgards, based on current listings on Migrate Mate as of July 2026. Columbus's hiring mix is broad, covering regional financial institutions, large retail and insurance companies headquartered here, and a growing cluster of SaaS and health tech startups.
Are there remote qa engineer jobs in Columbus?
Yes, qa engineer roles are well suited to remote and hybrid arrangements because the core work, writing test plans, running automated suites, and logging defects, is entirely screen-based. About 33% of qa engineer openings tied to Columbus are remote or hybrid as of July 2026, reflecting how broadly this flexibility has been adopted. Automation-focused and SDET roles within Columbus's fintech and health tech sectors tend to offer the most remote-friendly schedules.
How can I get a qa engineer job in Columbus with little or no experience?
The most realistic entry path in Columbus is targeting junior QA analyst or manual tester roles at mid-size software shops and insurance technology firms, which hire more entry-level candidates than large enterprise employers. Companies in the Columbus startup scene, particularly those around the Short North and the Columbus Collaboratory ecosystem, are more willing to train candidates who show strong attention to detail and basic scripting ability. Building a small portfolio of personal test cases or contributing to open-source projects can substitute for formal experience when applying locally.
Which industries hire the most qa engineers in Columbus?
The sectors hiring the most qa engineers in Columbus are Banking & Financial Services, Fintech, and Education, based on current listings on Migrate Mate as of July 2026. Columbus's role as a hub for large financial services firms, a major insurance industry center, and a growing health IT ecosystem creates consistent and varied demand for qa professionals across software development lifecycles.
See All 17 QA Engineer Jobs in Columbus
Find roles in Columbus that match your experience and apply in just a few clicks.
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