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# Senior Associate-Quality Assurance

- **Company:** Elanco Animal Health Incorporated
- **Location:** Clinton, IN, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Document Management Systems, Model Validation
- **Published:** August 14, 2026
- **Apply:** https://www.disabledperson.com/jobs/74244296-senior-associate-quality-assurance

## About the Role

* 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

## Description

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., * 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.


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