Top 16 Quality control validation Jobs in Columbus

Principal Specialist, Quality Assurance - Microbiology
Cardinal Health —Lewis Center, OH
- $80,900 - $103,950 a year
- Bachelor's degree
- No degree
- Mentoring
- Paid parental leave
- Health savings account
6d
Quality Control Lab Manager
Cencora —Columbus, OH
- Full-time
- 7 years
- Writing skills
- Ability to lift 50 pounds
- Paid parental leave
- Health insurance
Quality Control Supervisor
Anduril Industries —Ashville, OH
- $74,000 - $99,000 a year
- Email
- 3 years
- Analysis skills
- Supervising experience
Quick Apply
Quality Assurance Specialist-Night Shift
New Horizons Baking Company —Columbus, OH
- $22.81 an hour
- Night shift
- Mid-level
- Ability to lift 50 pounds
- Ability to stand for extended periods
- Disability insurance
- Health insurance
Quick Apply
Quality & Continuous Improvement Assistant (1st Shift)
Kinetics Noise Control —Dublin, OH
- $23 - $24 an hour
- Overtime
- Microsoft Excel
- Microsoft Outlook
- ERP systems
Quick Apply
14d
Entry Level Validation Engineer
CAI —Columbus, OH
- $60,000 - $70,000 a year
- Full-time
- Customer service
- Team management
- Military encouraged
- Disability insurance
- Health insurance
Quick Apply
11h
Quality Inspection Supervisor
Anduril Industries —Ashville, OH
- $74,000 - $99,000 a year
- Email
- 3 years
- Analysis skills
- Supervising experience
Quick Apply
Quality & Continuous Improvement Assistant (2nd Shift)
Kinetics Noise Control —Dublin, OH
- $23 - $24 an hour
- Overtime
- Microsoft Excel
- Microsoft Outlook
- ERP systems
Quick Apply
14d
Quality Clerk
CEVALogistics —Groveport, OH
- $16.43 - $20.54 an hour
- Full-time
- Customer service
- Computer literacy
- High school diploma or GED
- Health savings account
- AD&D insurance
7d
Scientist II, QC Analytical (2nd Shift)
Forge Biologics —Columbus, OH
- Full-time
- 6 years
- Mid-level
- Master's degree
- Paid parental leave
- Disability insurance
Quick Apply
Staff Product Quality Engineer, Low Observables
Anduril Industries —Ashville, OH
- $143,000 - $191,000 a year
- Email
- Oracle
- Engineering
- Master's degree
Quick Apply
11h
Construction Manager - Quality Control
Legacy Professional Services —New Albany, OH
- Full-time
- Construction site
- 5 years
- Senior level
- Opportunities for advancement
Quick Apply
14d
QA/QC Specialist - Substation Design
GPD Group —Columbus, OH
- Driver's License
- Mentoring
- US work authorization
- Profit sharing
- Disability insurance
Quick Apply
Transmission Quality and Standards Engineer
GPD Group —Columbus, OH
- Civil engineering
- 6 years
- Analysis skills
- Profit sharing
- Disability insurance
Quick Apply
Data Quality Engineer
Kemper Insurance —Columbus, OH
- $99,000 - $164,800 a year
- Full-time
- Remote
- Computer science
- 6 years
- Computer Science
- Health insurance
- Dental insurance
Quick Apply

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Principal Specialist, Quality Assurance - Microbiology
Cardinal Health —Lewis Center, OH
Investigation Leadership: Independently lead out-of-specification (OOS) and trend investigations, performing thorough root cause analysis, driving effective…
$80,900 - $103,950 a year
6d
Quality Control Lab Manager
Cencora —Columbus, OH
Bachelor’s degree in chemistry or related field required. Coordinate with departmental leaders to develop appropriate corrective actions resulting from…

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Principal Specialist, Quality Assurance - Microbiology

Cardinal Health -
Lewis Center, OH

Apply Now

Job Details

$80,900 - $103,950 a year
6 days ago

Benefits

Paid parental leave
Health savings account
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Parental leave
Vision insurance

Qualifications

Incident investigation techniques for hazard identification
Data integrity assurance
Biology
Content creation for technical audiences
Investigations regulatory compliance
Quality records maintenance
Defect resolution root cause analysis
Cleanroom environmental monitoring
Procedural guides
Pharmaceutical laboratory environment
Preventive action implementation
Testing and evaluation
Microbiology testing
Technical writing experience within manufacturing
Production deviation management
Good documentation practices (GDP)
Quality control preventive actions
Corrective and preventive actions (CAPA)
GMP
Internal investigations
Trend analysis
Microbiology
Bachelor's degree in biology
Quality reports
Data quality management
Policy & process development
Bachelor's degree
Pharmaceutical company experience
Team training
Quality improvement

Full Job Description

What Quality Assurance contributes to Cardinal Health

Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications.

Quality Assurance develops and implements a compliant and cost effective quality system that assures products and services are reliable, safe and effective. This job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on Quality policies and procedures and ensures that all products and services are properly reviewed for quality and documented.

Job Summary

We are seeking a highly motivated and detail-oriented Microbiology Principal Specialist to join our Quality team supporting PET facilities and Microbiology laboratory. This role is crucial for maintaining compliance with cGMP regulations and internal quality standards by reviewing and managing critical quality documentation. The ideal candidate will be a technical resource, leading investigations, driving corrective actions, and contributing to operational excellence initiatives. The Principal Specialist supports audit readiness and collaborates cross-functionally to enhance operational excellence and ensure data integrity, ultimately safeguarding product safety and efficacy. Additionally, this individual will provide secondary support for identification, media, and other microbiological method testing within the microbiology department.

The Principal Specialist plays a pivotal role in Cardinal Health's PET facilities' Quality Assurance, ensuring rigorous compliance with cGMP regulations and internal quality standards. This is achieved through meticulous management of quality documentation, application of microbiology expertise for product safety, and proactive identification and resolution of issues via investigation leadership and root cause analysis. These core Quality Assurance activities are critical for maintaining product quality, mitigating risks, and upholding the company's commitment to delivering safe and effective products.

Furthermore, this role significantly contributes to the overall Quality Assurance system by fostering cross-functional collaboration, ensuring data integrity, and supporting audit readiness. Within the Quality Assurance framework, this specialist is a vital technical resource, providing crucial support for manufacturing investigations and driving process improvements. Their work is fundamental to fortifying Cardinal Health's robust quality system, optimizing manufacturing efficiency, and upholding its reputation for reliability and patient safety

Responsibilities

Quality Documentation & Compliance: Author, review, and manage deviations, CAPAs, technical reports, SOP updates, and other microbiology-related documentation to ensure strict compliance with cGMP regulations, principles, and internal quality standards for Cardinal Health PET facilities
Microbiology Expertise: Apply and, ideally, possess experience or knowledge in product microbiology method validation (e.g., Bioburden, BET, sterility methods) and microbiology identification
Environmental Monitoring Trend Analysis: Review periodic Environmental Monitoring (EM) trend analysis for PET facilities, identifying and escalating negative trends to management
Investigation Leadership: Independently lead out-of-specification (OOS) and trend investigations, performing thorough root cause analysis, driving effective corrective and preventive actions, and ensuring clear, concise, and inspection-ready technical writing
Cross-Functional Collaboration: Partner closely with Manufacturing, Quality Assurance, Engineering, Validation, Training, and Supply Chain teams to support timely investigation closure, process improvements, and manufacturing readiness
Data Integrity & GDP: Ensure all documentation adheres to strict Good Documentation Practices (GDP) and ALCOA+ principles, demonstrating a strong understanding of data integrity
Audit & Inspection Readiness: Support audit and inspection readiness activities by providing documentation support and responding to quality system inquiries
Operational Excellence: Participate in initiatives focused on process simplification, documentation standardization, and right-first-time execution
Technical Support: Provide support to all PET manufacturing for investigations, fact-finding activities, troubleshooting, and Microbiology assessments
System Utilization: Utilize manufacturing and quality systems as required, including eBR, Veeva, SAP, and Microsoft Office applications, to manage records and track timelines
Training Support: Support training initiatives related to investigation findings, deviation writing, documentation practices, and GMP compliance expectations
Works on complex projects of large scope
Develops technical solutions to a wide range of difficult problems
Solutions are innovative and consistent with organization objectives
Completes work; independently receives general guidance on new projects
Work reviewed for purpose of meeting objectives
May act as a mentor to less experienced colleagues

Qualifications

Bachelor's degree in microbiology, Biology, or a related scientific field, preferred
4-8 years of experience, preferred
Proven experience in a cGMP regulated environment, preferably within the pharmaceutical or medical device industry
Comprehensive knowledge and thorough understanding of cGMP concepts, principles, and technical capabilities
Demonstrated ability to lead investigations and perform root cause analysis using recognized methodologies (e.g., 5-Whys, Fishbone diagrams)
Basic knowledge of Data Integrity & GDP and ALCOA+ principles
Excellent technical writing and communication skills
Ability to work effectively in a cross-functional team environment
Proficiency in using quality management systems (e.g., Veeva) and enterprise resource planning (ERP) systems (e.g., SAP) is a plus
Strong organizational skills and attention to detail

What is expected of you and others at this level

Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects
May contribute to the development of policies and procedures
Works on complex projects of large scope
Develops technical solutions to a wide range of difficult problems
Solutions are innovative and consistent with organization objectives
Completes work; independently receives general guidance on new projects
Work reviewed for purpose of meeting objectives
May act as a mentor to less experienced colleagues

Anticipated salary range: $80,900 - $103,950

Bonus eligible: No

Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

Medical, dental and vision coverage
Paid time off plan
Health savings account (HSA)
401k savings plan
Access to wages before pay day with myFlexPay
Flexible spending accounts (FSAs)
Short- and long-term disability coverage
Work-Life resources
Paid parental leave
Healthy lifestyle programs

Application window anticipated to close: 09/21/2026 *if interested in opportunity, please submit application as soon as possible.

The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

Apply Now

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quality control validation jobs in columbus

Principal Specialist, Quality Assurance - Microbiology

Quality Control Lab Manager

Quality Control Supervisor

Quality Assurance Specialist-Night Shift

Quality & Continuous Improvement Assistant (1st Shift)

Entry Level Validation Engineer

Quality Inspection Supervisor

Quality & Continuous Improvement Assistant (2nd Shift)

Quality Clerk

Scientist II, QC Analytical (2nd Shift)

Staff Product Quality Engineer, Low Observables

Construction Manager - Quality Control

QA/QC Specialist - Substation Design

Transmission Quality and Standards Engineer

Data Quality Engineer

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