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Verista, Inc. is seeking a QA Specialist to join our team in the Raleigh/Durham, NC area. You will ensure quality and regulatory compliance across pharmaceutical processes, equipment, and documentation.
The role requires hands-on experience with cGMP, GDP and audits, along with strong CAPA and deviation management skills. The ideal candidate has 3+ years in QA within pharma or biotech, is detail-oriented, and committed to patient safety and regulatory excellence.
Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision‑making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world‑class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
Join Our Team: QA Specialists Wanted in Raleigh/Durham, NC!
Are you a skilled QA Specialist with a passion for ensuring quality in the pharmaceutical industry? Verista is actively seeking talented professionals to join our team in the vibrant Raleigh/Durham, NC area!
Who We’re Looking For:
What We Offer:
Why Choose Verista?
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com