Quality Assurance Intern Jobs in Kentucky
Quality Assurance Intern jobs in Kentucky concentrate in manufacturing, automotive supply chain, food and beverage production, and healthcare, with the strongest demand found in Louisville, Lexington, and the Northern Kentucky corridor near Cincinnati. Major employers with a lasting presence in the state, including Toyota, Humana, and Ashland, regularly bring on quality assurance interns across production verification, documentation control, and regulatory compliance work. Openings exist across experience levels, from first-semester undergraduates to seniors completing capstone projects. See the openings below and apply to the ones that match your experience.
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Showing 5 of 22+ Quality Assurance Intern jobs
About Site
Catalent’s Winchester, KY site is the company’s flagship U.S. manufacturing location for large‑scale oral solid dose forms, operating from a 180,000‑square‑foot facility with fully integrated development and analytical services. The site specializes in complex and controlled‑release oral dose technologies, supporting product development, technology transfer, and commercial manufacturing across pharmaceutical and consumer health programs. Winchester has a long commercial manufacturing track record, having launched 100+ products and producing billions of tablets and capsules annually, making it a critical site within Catalent’s oral dose network.
Position Summary
We have an opportunity for a Supervisor, Quality Assurance to join our team at the Winchester, KY site. This role provides leadership and supervision within the Quality Assurance function, ensuring compliance with Quality Systems, Finished Product Batch Release, and Change Control. The position supports regulatory inspections, customer audits, and continuous improvement initiatives. It’s a great opportunity to contribute to a high‑performing team dedicated to maintaining the highest standards of quality and compliance.
Shift: Monday-Friday, 2 PM - 10:30 PM
Location: Winchester, KY
100% Onsite
The Role
- Ensure Quality systems comply with corporate and site procedures as well as industry standards, including Annual Product Reviews, Complaints, Investigations, Corrective and Preventive Actions, and Training.
- Supervise the Quality Assurance Associates.
- Participate in Regulatory (FDA) Inspections and Customer Audits.
- Author and maintain detailed Standard Operating Procedures defining Winchester’s Quality Systems.
- Facilitate Investigations, root cause analysis, Complaints process, and Annual Product Review process.
- Manage and track documentation of Corrective and Preventive Action commitments and related trending processes.
- Recommend process changes based on trends from CAPA, Complaints, and Annual Product Reviews.
- Serve as the Quality department liaison and subject matter expert to other departments, customers, and regulatory representatives.
- Act as subject matter expert in TrackWise, Documentum, and other Quality software platforms.
- Communicate and implement Human Resources policies within the department.
- Maintain documentation related to employee performance and timekeeping, and administer discipline as appropriate in coordination with Human Resources.
- Ensure adherence to quality standards governed by current Good Manufacturing Practices, company Quality Policies, and site Standard Operating Procedures.
- Propose, implement, and enforce quality improvements.
- Perform other duties as required.
The Candidate
Minimum Requirements
- Bachelor's Degree with 2+ years of related work experience; OR Associate Degree with 3+ years of related work experience; OR High School Diploma/GED with 4+ years of related work experience.
- Batch review and cGMP experience totaling 2+ years.
- Strong analytical and investigative skills.
- Proficient in English verbal and written communication skills to convey and receive ideas and instructions within and outside the organization.
- Proficiency in Microsoft Word, PowerPoint, Excel, and Access.
- Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
- Physical Requirements: Individual may be required to sit for an extended period of time. Specific vision requirements include reading of written documents and frequent use of computer monitor. Sustained sitting at desk or workstation with use of phones, computers, and other office equipment required for the position. Static stance/standing as required. File/folder storage with non‑repetitive light weight lifting, reaching, and forward bending as necessary. Infrequent overhead lifting less than or equal to 15 lbs with the ability to lift up to 35 lbs and push/pull 40 lbs.
Preferred Skills & Background
- Prior supervisory or management experience (will immediately have 5 reports).
- TrackWise Quality Management System experience.
- Strong technical writing skills for investigations, deviations, Corrective and Preventive Actions, and root cause analysis.
- Bachelor’s degree in Life Science.
Why You Should Join Catalent
- Positive and fast‑paced working environment focusing on continual improvement and innovation.
- Competitive Paid Time Off plus 8 paid holidays.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement – support to complete or earn a new degree.
- Site‑based Employee Engagement activities such as NCAA Basketball Brackets, Golf Scrambles, Annual Onsite Pet Adoption Events, and Mentorship Partnerships with Local Schools.
- Employee Resource Groups focusing on Diversity and Inclusion.
- Environmentally friendly community engagement initiatives, including Adopt‑a‑Highway Clean‑up participation.
- Defined career path with annual performance reviews and growth potential within an organization dedicated to improving lives.
- WellHub program promoting physical and mental wellness.
- Perkspot offering exclusive discounts from over 900 merchants across various categories.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
About Site
Catalent’s Winchester, KY site is the company’s flagship U.S. manufacturing location for large‑scale oral solid dose forms, operating from a 180,000‑square‑foot facility with fully integrated development and analytical services. The site specializes in complex and controlled‑release oral dose technologies, supporting product development, technology transfer, and commercial manufacturing across pharmaceutical and consumer health programs. Winchester has a long commercial manufacturing track record, having launched 100+ products and producing billions of tablets and capsules annually, making it a critical site within Catalent’s oral dose network.
Position Summary
We have an opportunity for a Supervisor, Quality Assurance to join our team at the Winchester, KY site. This role provides leadership and supervision within the Quality Assurance function, ensuring compliance with Quality Systems, Finished Product Batch Release, and Change Control. The position supports regulatory inspections, customer audits, and continuous improvement initiatives. It’s a great opportunity to contribute to a high‑performing team dedicated to maintaining the highest standards of quality and compliance.
Shift: Monday-Friday, 2 PM - 10:30 PM
Location: Winchester, KY
100% Onsite
The Role
- Ensure Quality systems comply with corporate and site procedures as well as industry standards, including Annual Product Reviews, Complaints, Investigations, Corrective and Preventive Actions, and Training.
- Supervise the Quality Assurance Associates.
- Participate in Regulatory (FDA) Inspections and Customer Audits.
- Author and maintain detailed Standard Operating Procedures defining Winchester’s Quality Systems.
- Facilitate Investigations, root cause analysis, Complaints process, and Annual Product Review process.
- Manage and track documentation of Corrective and Preventive Action commitments and related trending processes.
- Recommend process changes based on trends from CAPA, Complaints, and Annual Product Reviews.
- Serve as the Quality department liaison and subject matter expert to other departments, customers, and regulatory representatives.
- Act as subject matter expert in TrackWise, Documentum, and other Quality software platforms.
- Communicate and implement Human Resources policies within the department.
- Maintain documentation related to employee performance and timekeeping, and administer discipline as appropriate in coordination with Human Resources.
- Ensure adherence to quality standards governed by current Good Manufacturing Practices, company Quality Policies, and site Standard Operating Procedures.
- Propose, implement, and enforce quality improvements.
- Perform other duties as required.
The Candidate
Minimum Requirements
- Bachelor's Degree with 2+ years of related work experience; OR Associate Degree with 3+ years of related work experience; OR High School Diploma/GED with 4+ years of related work experience.
- Batch review and cGMP experience totaling 2+ years.
- Strong analytical and investigative skills.
- Proficient in English verbal and written communication skills to convey and receive ideas and instructions within and outside the organization.
- Proficiency in Microsoft Word, PowerPoint, Excel, and Access.
- Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
- Physical Requirements: Individual may be required to sit for an extended period of time. Specific vision requirements include reading of written documents and frequent use of computer monitor. Sustained sitting at desk or workstation with use of phones, computers, and other office equipment required for the position. Static stance/standing as required. File/folder storage with non‑repetitive light weight lifting, reaching, and forward bending as necessary. Infrequent overhead lifting less than or equal to 15 lbs with the ability to lift up to 35 lbs and push/pull 40 lbs.
Preferred Skills & Background
- Prior supervisory or management experience (will immediately have 5 reports).
- TrackWise Quality Management System experience.
- Strong technical writing skills for investigations, deviations, Corrective and Preventive Actions, and root cause analysis.
- Bachelor’s degree in Life Science.
Why You Should Join Catalent
- Positive and fast‑paced working environment focusing on continual improvement and innovation.
- Competitive Paid Time Off plus 8 paid holidays.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement – support to complete or earn a new degree.
- Site‑based Employee Engagement activities such as NCAA Basketball Brackets, Golf Scrambles, Annual Onsite Pet Adoption Events, and Mentorship Partnerships with Local Schools.
- Employee Resource Groups focusing on Diversity and Inclusion.
- Environmentally friendly community engagement initiatives, including Adopt‑a‑Highway Clean‑up participation.
- Defined career path with annual performance reviews and growth potential within an organization dedicated to improving lives.
- WellHub program promoting physical and mental wellness.
- Perkspot offering exclusive discounts from over 900 merchants across various categories.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
See All 22 Quality Assurance Intern Jobs in Kentucky
Find roles in Kentucky that match your experience and apply in just a few clicks.
Find Quality Assurance Intern JobsQuality Assurance Intern Jobs by City in Kentucky
Where Kentucky roles are concentrated, by current openings.
Quality Assurance Intern Job Market in Kentucky
A snapshot from current Kentucky openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Construction & Real Estate
What Kentucky Employers Look For
The qualifications that appear most often in quality assurance intern jobs across Kentucky.
- Currently enrolled in a bachelor's degree program in engineering, science, or a related field
- Familiarity with quality management principles such as ISO standards or Six Sigma methodology
- Ability to read and interpret technical drawings, specifications, or standard operating procedures
- Proficiency with Microsoft Office tools, particularly Excel for data entry and reporting
- Strong attention to detail and experience with inspection, testing, or documentation tasks
- Availability to work on-site at a Kentucky facility for the duration of the internship term
Quality Assurance Intern Jobs in Kentucky: Frequently Asked Questions
How do you become a quality assurance intern in Kentucky?
Most quality assurance intern positions in Kentucky do not require a state-issued license, but employers expect enrollment in an accredited engineering, manufacturing technology, life sciences, or business program at a Kentucky university or community college. Programs at the University of Kentucky, University of Louisville, or Kentucky Community and Technical College System align well with what local manufacturers and healthcare organizations look for. Completing coursework in statistics, process improvement, or regulatory compliance gives candidates a clear advantage in the Kentucky market.
Which companies hire quality assurance interns in Kentucky?
Kentucky quality assurance intern roles are posted by IPG, Atkore, and Maximus and others right now, based on current listings on Migrate Mate as of November 2026. Kentucky's dense concentration of automotive, food production, and healthcare employers means intern opportunities appear across a wider range of industries here than in many other states.
Which Kentucky cities have the most quality assurance intern jobs?
Louisville, Kentucky, and Benton account for the largest share of quality assurance intern openings in Kentucky. Louisville leads because of its headquarters-level corporate presence and large healthcare and logistics base, while Lexington draws demand from life sciences and manufacturing employers, and the Northern Kentucky area benefits from its proximity to major Cincinnati-region supply chain and distribution operations.
Are there remote quality assurance intern jobs in Kentucky?
Yes, but they're limited. Quality assurance work is largely hands-on, tied to factory floors, labs, or regulated facilities, so fully remote positions are uncommon. About 44% of quality assurance intern openings tied to Kentucky are remote or hybrid as of November 2026, which is below average for internship roles generally. The portions most likely to allow remote work involve documentation review, data analysis, and audit preparation rather than physical inspection.
How can I get hired as a quality assurance intern in Kentucky with little or no experience?
The most realistic entry path is applying directly through your university's co-op or internship office, since Toyota Manufacturing Kentucky, Ashland, and several Louisville-area healthcare systems run structured intern programs designed for students without prior work history. Adjacent experience in warehouse receiving, laboratory assistance, or production floor support translates well and is commonly listed as acceptable in Kentucky postings. Completing an introductory Six Sigma or ISO awareness course before applying signals readiness to Kentucky employers who weight process knowledge heavily.
Where can I find and apply to quality assurance intern jobs in Kentucky?
You can find and apply to quality assurance intern jobs in Kentucky on Migrate Mate, which lists current openings from employers actively hiring in the state. Search the listings, identify roles that fit your background and location, and apply directly to the ones that match. No signup is needed to see the openings.
See All 22 Quality Assurance Intern Jobs in Kentucky
Find roles in Kentucky that match your experience and apply in just a few clicks.
Find Quality Assurance Intern Jobs