QA Specialist Jobs in Indiana
QA Specialist jobs in Indiana are concentrated in Indianapolis, Fort Wayne, and Elkhart, where manufacturing, medical devices, and life sciences drive consistent demand for quality professionals at every level from entry-level inspectors to senior quality engineers. Companies like Eli Lilly, Cummins, and Zimmer Biomet maintain deep quality assurance teams across Indiana and recruit regularly for specialists in software testing, regulatory compliance, and production quality control. Demand is strong across both the manufacturing corridor in northern Indiana and the healthcare and tech sectors in the Indianapolis metro. Find a role that fits below and apply directly.
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Showing 5 of 73+ QA Specialist jobs
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Senior Associate – Quality Assurance
As a Senior QA Representative, you will be part of the Clinton Quality Control Unit to deliver essential support for quality systems and GMP compliance. In this role, you’ll be responsible for advancing laboratory investigations, method validation, and continuous improvement initiatives through coaching and change control implementation.
Your Responsibilities:
Provide quality control support by providing assistance and guidance in laboratory investigations, Product Quality Reviews (PQR), and method validation activities.
Maintain GMP compliance and inspection readiness for regulatory agencies through periodic audits and inspections of production areas.
Facilitate continuous improvement by authoring and supporting deviation investigations and implementing change control proposals.
Collaborate effectively across cross-functional QC teams, including laboratory technicians, chemists, and analysts, to ensure quality standards.
Investigate customer complaints and review critical quality documents, including validation and PQR .
Support and strengthen site Quality Systems by writing and revising SOPs, delivering site training, conducting internal audits, verifying inspection readiness, monitoring quality metrics, and representing the site in corporate knowledge-sharing forums.
What You Need to Succeed (minimum qualifications):
Education: Bachelor’s degree in Chemistry , Biology, Pharmacy, or a related scientific field
Experience: A minimum of 2 years of experience in Quality Assurance, Quality Control, or a regulated GMP manufacturing environment
Top Skills: Proficiency in cGMP regulations and experience with quality documentation systems
What Will Give You a Competitive Edge (preferred qualifications):
Experience coaching or providing technical feedback to QC staff
Proven ability to handle non-standard requests and participate in regulatory audits
Strong technical writing skills for authoring validation and PQR documents
Experience with change control implementation and deviation management
Demonstrated ability to work effectively in cross-functional team environments
Additional Information:
Location: Clinton, IN – Onsite Manufacturing Facility
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
Multiple relocation packages
Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
8-week parental leave
9 Employee Resource Groups
Annual bonus offering
Up to 6% 401K matching
#LI-KG2
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Senior Associate – Quality Assurance
As a Senior QA Representative, you will be part of the Clinton Quality Control Unit to deliver essential support for quality systems and GMP compliance. In this role, you’ll be responsible for advancing laboratory investigations, method validation, and continuous improvement initiatives through coaching and change control implementation.
Your Responsibilities:
Provide quality control support by providing assistance and guidance in laboratory investigations, Product Quality Reviews (PQR), and method validation activities.
Maintain GMP compliance and inspection readiness for regulatory agencies through periodic audits and inspections of production areas.
Facilitate continuous improvement by authoring and supporting deviation investigations and implementing change control proposals.
Collaborate effectively across cross-functional QC teams, including laboratory technicians, chemists, and analysts, to ensure quality standards.
Investigate customer complaints and review critical quality documents, including validation and PQR .
Support and strengthen site Quality Systems by writing and revising SOPs, delivering site training, conducting internal audits, verifying inspection readiness, monitoring quality metrics, and representing the site in corporate knowledge-sharing forums.
What You Need to Succeed (minimum qualifications):
Education: Bachelor’s degree in Chemistry , Biology, Pharmacy, or a related scientific field
Experience: A minimum of 2 years of experience in Quality Assurance, Quality Control, or a regulated GMP manufacturing environment
Top Skills: Proficiency in cGMP regulations and experience with quality documentation systems
What Will Give You a Competitive Edge (preferred qualifications):
Experience coaching or providing technical feedback to QC staff
Proven ability to handle non-standard requests and participate in regulatory audits
Strong technical writing skills for authoring validation and PQR documents
Experience with change control implementation and deviation management
Demonstrated ability to work effectively in cross-functional team environments
Additional Information:
Location: Clinton, IN – Onsite Manufacturing Facility
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
Multiple relocation packages
Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
8-week parental leave
9 Employee Resource Groups
Annual bonus offering
Up to 6% 401K matching
#LI-KG2
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
See All 73 QA Specialist Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find QA Specialist JobsQA Specialist Jobs by City in Indiana
Where Indiana roles are concentrated, by current openings.
QA Specialist Job Market in Indiana
A snapshot from current Indiana openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Food & Beverage
- Biotechnology & Pharmaceuticals
- Distribution & Wholesale
- Investment & Asset Management
- Automotive
What Indiana Employers Look For
The qualifications that appear most often in QA specialist jobs across Indiana.
- Bachelor's degree in engineering, life sciences, or a related technical field
- Demonstrated experience with quality management systems such as ISO 9001 or AS9100
- Proficiency in statistical process control and root cause analysis methods
- Familiarity with FDA regulations and GMP requirements for regulated Indiana industries
- Experience using QA tools such as JIRA, TestRail, or similar defect tracking software
- Strong written communication skills for documenting test plans and nonconformance reports
QA Specialist Jobs in Indiana: Frequently Asked Questions
How do you become a qa specialist in Indiana?
Most qa specialist roles in Indiana require at least a bachelor's degree in engineering, quality management, life sciences, or a closely related field. While Indiana does not issue a state license specifically for qa specialists, employers in regulated sectors like medical devices and pharmaceuticals strongly favor candidates who hold a Certified Quality Auditor or Certified Quality Engineer credential from the American Society for Quality. Building familiarity with ISO standards and FDA regulations early significantly improves hiring prospects.
Which companies hire qa specialists in Indiana?
Indiana qa specialist roles are posted by Bunge, Eli Lilly, and Superior Essex and others right now, based on current listings on Migrate Mate as of August 2026. Indiana's manufacturing base and life sciences sector mean that employers range from large pharmaceutical companies in Indianapolis to precision manufacturers and medical device firms in the northern part of the state.
Which Indiana cities have the most qa specialist jobs?
Indianapolis, Fort Wayne, and Evansville have the most qa specialist openings in Indiana right now. Indianapolis leads because it anchors the state's life sciences and tech industries, while Fort Wayne and Elkhart draw qa roles from the dense manufacturing and automotive supplier base in northern Indiana, where large production facilities require dedicated quality teams.
Are there remote qa specialist jobs in Indiana?
Yes, but they are less common than in purely desk-based fields, since many qa specialist roles require on-site inspection, lab access, or direct observation of production lines. About 28% of qa specialist openings tied to Indiana are remote or hybrid as of August 2026, which reflects the role's mix of hands-on and analytical work. Software QA and documentation-heavy compliance roles are the most likely to offer remote or hybrid arrangements.
How can I get hired as a qa specialist in Indiana with little or no experience?
The most realistic entry path is a quality technician or quality inspector position, which many Indiana manufacturers use as a feeder role before promoting into specialist titles. Companies like Cummins and Zimmer Biomet run structured early-career and rotational programs in Indiana that welcome candidates without direct QA experience. Lateral moves from production, laboratory technician, or supply chain roles are common. Earning an entry-level quality credential from the American Society for Quality and building a portfolio of any process improvement or audit work gives candidates a measurable edge in Indiana hiring.
Where can I find and apply to qa specialist jobs in Indiana?
You can find and apply to qa specialist jobs in Indiana on Migrate Mate, which lists current Indiana openings across manufacturing, life sciences, tech, and other sectors. Find roles that fit your background and apply directly to the ones that match.
See All 73 QA Specialist Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find QA Specialist Jobs