Quality Assurance Engineer Jobs in Indianapolis, IN
Quality Assurance Engineer jobs in Indianapolis are concentrated in the Meridian-Kessler technology corridor, the North Meridian Street healthcare belt, and the Keystone suburban office parks, with strong demand across medical devices, automotive software, and enterprise SaaS. Employers actively hiring include Cardinal Health, Elanco, and American Technology Consulting. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 20+ Quality Assurance Engineer jobs
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results.
We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory.
It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow.
Learn about the Danaher Business System which makes everything possible.
The Staff Quality Assurance Engineer is responsible for owning quality related processes, guiding cross-functional teams through Beckman’s quality management system requirements, and ensuring product quality for Beckman’s customers.
This position reports to the Senior Manager Manufacturing Quality and is part of the Quality & Regulatory Affairs organization located in Indianapolis, IN. This will be an on-site role.
In this role, you will have the opportunity to:
Represent Quality Assurance on cross functional teams tasked with business critical initiatives ranging from quality improvement projects to new product transfers and launches.
Apply your insight of current industry standards and regulations and how they relate to internal policies and procedures. Influence interpretation of internal policies and procedures to ensure quality and compliance.
Serve as a local process owner and subject matter expert for Production & Process Controls as well as other manufacturing related QMS processes.
Coach teams with application of ISO 9001/13485/cGMP and quality systems processes throughout product lifecycle
Leverage data analytics and business intelligence tools to identify quality trends, monitor process performance, drive risk-based decision making, and communicate actionable insights to leadership
The essential requirements of the job include:
Demonstrated experience supporting the manufacture of medical device instruments, electromechanical systems, laboratory instrumentation, diagnostic analyzers, automation platforms, or similar complex medical devices.
Proven experience applying quality and regulatory requirements to manufacturing processes, process validation, equipment qualification, nonconformance management, CAPA, risk management, and continuous improvement activities.
Working knowledge of ISO 9001 & ISO 13485 standards, and 21 CFR Part 820 & EU MDR/IVDR regulations
Bachelor’s Degree (minimum) in engineering or other science or related field; or equivalent experience required.
7+ years' experience (or 4+ years with Master's Degree) in Quality Engineering, Manufacturing Engineering, or Quality Systems within regulated industries.
Travel, Motor Vehicle Record & Physical/Environment Requirements:
Travel requirements < 20% of the time, domestic and international
Overnight travel may be required
Be able to occasionally lift and/or move up to 40 pounds.
It would be a plus if you also possess previous experience in:
Advanced Power BI (or similar) capabilities including data modeling, DAX development, Power Query, dashboard design, KPI development, and integration of data from ERP, eQMS, manufacturing, and other enterprise systems
Quality Engineering tools such as Six Sigma, DMAIC, Statistical Process Control, 5 why’s, 8D, PFMEA, Design of Experiment, etc.
Oracle as an ERP and IQVIA as an eQMS
Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results.
We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory.
It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow.
Learn about the Danaher Business System which makes everything possible.
The Staff Quality Assurance Engineer is responsible for owning quality related processes, guiding cross-functional teams through Beckman’s quality management system requirements, and ensuring product quality for Beckman’s customers.
This position reports to the Senior Manager Manufacturing Quality and is part of the Quality & Regulatory Affairs organization located in Indianapolis, IN. This will be an on-site role.
In this role, you will have the opportunity to:
Represent Quality Assurance on cross functional teams tasked with business critical initiatives ranging from quality improvement projects to new product transfers and launches.
Apply your insight of current industry standards and regulations and how they relate to internal policies and procedures. Influence interpretation of internal policies and procedures to ensure quality and compliance.
Serve as a local process owner and subject matter expert for Production & Process Controls as well as other manufacturing related QMS processes.
Coach teams with application of ISO 9001/13485/cGMP and quality systems processes throughout product lifecycle
Leverage data analytics and business intelligence tools to identify quality trends, monitor process performance, drive risk-based decision making, and communicate actionable insights to leadership
The essential requirements of the job include:
Demonstrated experience supporting the manufacture of medical device instruments, electromechanical systems, laboratory instrumentation, diagnostic analyzers, automation platforms, or similar complex medical devices.
Proven experience applying quality and regulatory requirements to manufacturing processes, process validation, equipment qualification, nonconformance management, CAPA, risk management, and continuous improvement activities.
Working knowledge of ISO 9001 & ISO 13485 standards, and 21 CFR Part 820 & EU MDR/IVDR regulations
Bachelor’s Degree (minimum) in engineering or other science or related field; or equivalent experience required.
7+ years' experience (or 4+ years with Master's Degree) in Quality Engineering, Manufacturing Engineering, or Quality Systems within regulated industries.
Travel, Motor Vehicle Record & Physical/Environment Requirements:
Travel requirements < 20% of the time, domestic and international
Overnight travel may be required
Be able to occasionally lift and/or move up to 40 pounds.
It would be a plus if you also possess previous experience in:
Advanced Power BI (or similar) capabilities including data modeling, DAX development, Power Query, dashboard design, KPI development, and integration of data from ERP, eQMS, manufacturing, and other enterprise systems
Quality Engineering tools such as Six Sigma, DMAIC, Statistical Process Control, 5 why’s, 8D, PFMEA, Design of Experiment, etc.
Oracle as an ERP and IQVIA as an eQMS
Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
See All 20 Quality Assurance Engineer Jobs in Indianapolis
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Find JobsQuality Assurance Engineer Job Market in Indianapolis
Who's Hiring
Top Industries Hiring
- Distribution & Wholesale
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
Quality Assurance Engineer Jobs in Indianapolis: Frequently Asked Questions
How do I get a quality assurance engineer job in Indianapolis?
Focus on Indianapolis's strongest hiring sectors: medical device manufacturing, automotive technology suppliers, and enterprise software companies clustered along the North Meridian corridor and in Carmel and Fishers. Candidates who can demonstrate hands-on experience with regulated environments, such as FDA quality systems or ISO standards, stand out here because so many local employers operate under compliance-heavy frameworks. Networking through Indiana tech meetups and the local PMI chapter also surfaces roles before they post publicly.
Which companies hire quality assurance engineers in Indianapolis?
Indianapolis quality assurance engineer roles are posted by Cardinal Health, Elanco, and American Technology Consulting and others right now, based on current listings on Migrate Mate as of July 2026. The Indianapolis market draws from a broad mix of large medical device manufacturers, regional insurance technology firms, and mid-size automotive software suppliers, all of which maintain dedicated QA functions.
Are there remote quality assurance engineer jobs in Indianapolis?
Yes, though availability depends heavily on the specialty: software and automation QA roles are commonly remote, while roles tied to physical product testing or regulated manufacturing lines require on-site presence. About 30% of quality assurance engineer openings tied to Indianapolis are remote or hybrid as of July 2026, with the most flexible arrangements found at SaaS and insurtech employers concentrated near downtown and the Carmel tech corridor.
How can I get a quality assurance engineer job in Indianapolis with little or no experience?
The most realistic entry path locally is through Indianapolis's medical device and life sciences employers, many of which hire quality technicians and junior compliance associates as stepping stones into full QA engineer roles. Completing a quality-focused certification such as ASQ's Certified Quality Technician and targeting contract-to-hire positions at staffing firms that serve Eli Lilly's supplier network or Cook Medical gives entry-level candidates a concrete foothold. Building familiarity with FDA 21 CFR Part 820 documentation practices makes an early-career candidate noticeably more competitive in Indianapolis specifically.
Which industries hire the most quality assurance engineers in Indianapolis?
Most quality assurance engineer openings in Indianapolis sit in Distribution & Wholesale, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, per current listings on Migrate Mate as of July 2026. Indianapolis's role as a hub for pharmaceutical manufacturing, automotive parts suppliers, and insurance technology companies creates sustained, year-round QA hiring across all three sectors.
Related Jobs in Indiana
See All 20 Quality Assurance Engineer Jobs in Indianapolis
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