6170 - Batch Disposition Associate / Quality Specialist
Verista, Inc.(7 days ago)
About this role
Verista is a life‑sciences consulting firm partnering with pharmaceutical and biotech organizations to advance regulated manufacturing and quality systems. The Quality Specialist is a QA team member who helps ensure regulatory compliance and supports Verista’s mission to enable life sciences clients to improve lives. This is an on-site, full-time position based in Durham, NC.
Required Skills
- Batch Review
- Deviation Management
- Change Control
- CAPA
- GMP
- Aseptic Manufacturing
- Trend Analysis
- Documentation Review
- Risk Assessment
- Quality Oversight
+1 more
Qualifications
- Bachelor's Degree (Life Sciences or related)
About Verista, Inc.
verista.comVerista is a life‑sciences consulting and engineering firm that supports pharmaceutical, biotech, medical device, and consumer‑health companies across the entire product lifecycle. They specialize in validation, quality and regulatory compliance, engineering and automation, commissioning/qualification, computer system validation, and digital transformation. Verista combines domain‑specific technical expertise and regulatory know‑how with hands‑on implementation to reduce risk, accelerate timelines, and ensure GxP compliance for complex manufacturing, clinical, and commercial operations.
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