Job Title: Quality Assurance Specialist
Location: Louisville, Kentucky (On-Site)
Job Summary: We are supporting a role for a detail-driven quality professional to help ensure compliance across warehouse operations, raw material handling, and documentation review. Our team is seeking someone who can provide hands-on oversight, support GMP expectations, and contribute to consistent quality outcomes in a fast-paced, regulated environment.
Responsibilities:
- Oversee warehouse activities related to incoming raw materials, inspection, sampling, and disposition decisions.
- Review receipt, storage, inspection, and distribution documentation to support compliance with GMP, GDP, and Good Documentation Practices.
- Provide routine quality assurance assessments, operational oversight, and guidance to cross-functional teams.
- Support audits, inspections, deviations, CAPAs, change controls, risk assessments, and validation records as required.
Required:
- 5+ years of QA experience specifically involving raw materials in a GMP-regulated environment such as pharmaceutical, biotech, or other life sciences industries.
- Bachelor’s degree strongly preferred; master’s degree may be considered.
- Must be able to work onsite daily in Easton, Pennsylvania; local candidates or self-relocation only, with no exceptions.
- Must be physically able to perform the role’s requirements, including passing an eye exam, lifting materials of approximately 40 lbs, and consistent gowning.
About SSI People: With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.
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