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QA Complaint Analyst

Integrated DNA Technologies
Integrated DNA Technologies Salary
Coralville, IA Full Time
POSTED ON 4/26/2025
AVAILABLE BEFORE 5/25/2025
Integrated DNA Technologies (IDT) is the leading manufacturer of custom oligonucleotides and proprietary technologies for genomics applications. Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we realize that although science may be uniform, people are unique. We promote a culture where engaged people are motivated and have opportunities to achieve their full potential, as part of one global team.

IDT is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.

This position is part of the Quality Assurance Department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things.

In this role, you will have the opportunity to:

  • Contribute to the continuous improvement of product safety compliance by effectively managing and resolving quality complaints
  • Communicate with internal team members and external customers to facilitate complaint investigation process.
  • Receive and document complaints from various sources, including customers, healthcare professionals, and internal stakeholders.
  • Work closely with cross-functional teams, including Scientific Application Support (SAS), Quality Assurance, Regulatory Affairs, Product Development, and manufacturing to investigate and resolve complaints.
  • Support quality system investigations, including issue reviews, nonconformances, CAPAs, SCARs, as needed.

The essential requirements of the job include:

  • Bachelor's degree in Biological Sciences or related field (e.g., Biomedical Engineering, Systems Engineering, Pharmacology, Chemistry)
  • 1 - 2 years of related experience in post-market product surveillance and complaint handling.

It would be a plus if you also possess previous experience in:

  • Proficient in data analysis and workflow troubleshooting, including instrumentation, arrays, and biological materials.
  • Experience with SAP is preferred. Proficiency in Microsoft Office Products (Word, Excel, PowerPoint) or equivalent software applications is preferred.
  • Familiarity with ISO 13485, 21 CFR 820, 21 CFR 803, and QSR quality management system requirements and IVD products.

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.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

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