QA Manager Jobs in Indiana
QA Manager jobs in Indiana represent a steady and competitive market, concentrated in manufacturing, life sciences, and medical devices, with openings at every level from team lead to senior director. Indianapolis, Fort Wayne, and Elkhart anchor most of the hiring, where established employers like Eli Lilly, Cummins, and Zimmer Biomet maintain significant quality and compliance operations. The most in-demand specialties are pharmaceutical quality systems, ISO-certified manufacturing, and software QA for the state's growing tech sector. Scan the live roles below and apply to whichever ones fit.
Find QA Manager JobsOverview
Showing 5 of 69+ QA Manager 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 69 QA Manager Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find QA Manager JobsQA Manager Jobs by City in Indiana
Where Indiana roles are concentrated, by current openings.
QA Manager Job Market in Indiana
A snapshot from current Indiana openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Food & Beverage
- Distribution & Wholesale
- Investment & Asset Management
- Biotechnology & Pharmaceuticals
- Automotive
What Indiana Employers Look For
The qualifications that appear most often in QA manager jobs across Indiana.
- Bachelor's degree in engineering, life sciences, or a related technical field required
- Five or more years of QA experience in manufacturing, medical devices, or pharmaceuticals
- Demonstrated knowledge of ISO 9001, FDA 21 CFR, or cGMP quality standards
- Experience leading audits, corrective action processes, and quality management systems
- Certified Quality Manager or Certified Quality Engineer credential preferred by most Indiana employers
- Strong data analysis skills and proficiency with quality software such as SAP or Minitab
QA Manager Jobs in Indiana: Frequently Asked Questions
How do you become a qa manager in Indiana?
Most Indiana employers require a bachelor's degree in a technical field such as engineering, chemistry, or life sciences, combined with several years of hands-on quality assurance experience. Indiana does not issue a state-specific license for qa managers, but professional certifications from the American Society for Quality, such as the Certified Quality Manager or Certified Quality Engineer designation, are widely recognized by Indiana manufacturers and medical device companies and significantly strengthen a candidate's profile.
Which companies hire qa managers in Indiana?
Companies currently hiring qa managers in Indiana include Bunge, Eli Lilly, and Superior Essex, per current listings on Migrate Mate as of August 2026. Indiana's strong concentration of pharmaceutical, medical device, and advanced manufacturing employers means qa manager demand is distributed well beyond Indianapolis, reaching mid-sized industrial cities like Columbus, Kokomo, and Anderson.
Which Indiana cities have the most qa manager jobs?
Indianapolis, Fort Wayne, and Evansville account for the most qa manager openings in Indiana. Indianapolis leads because it is home to major pharmaceutical and life sciences headquarters, while Fort Wayne and Elkhart generate consistent demand through their dense concentrations of automotive suppliers, RV manufacturers, and precision parts producers that require dedicated quality leadership.
Are there remote qa manager jobs in Indiana?
Yes, but they're rare. About 24% of qa manager openings tied to Indiana are remote or hybrid as of August 2026, reflecting the reality that most qa manager work involves direct oversight of production lines, lab environments, and physical audits. The parts of the role most likely to go remote are documentation review, supplier audits conducted by video, and quality system administration for software-focused organizations.
How can I get hired as a qa manager in Indiana with little or no experience?
The most realistic path is moving into a qa manager role from a quality technician, quality engineer, or production supervisor position at an Indiana manufacturer or life sciences company. Large Indiana employers like Eli Lilly and Zimmer Biomet run structured associate and rotational programs that place early-career candidates in quality functions. Earning an entry-level American Society for Quality certification, such as the Certified Quality Technician, signals commitment and gives candidates an edge when applying to those programs or to QA coordinator openings that lead directly into management.
Where can I find and apply to qa manager jobs in Indiana?
You can find and apply to qa manager jobs in Indiana on Migrate Mate, which lists current Indiana openings. Search the roles available, find the ones that match your experience and location, and apply directly to the ones that fit.
See All 69 QA Manager Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find QA Manager Jobs