Verista is seeking a Quality Assurance Specialist with over three years of experience in the pharmaceutical or biotech industries to join their team in Research Triangle Park, NC. The role focuses on ensuring compliance with regulatory standards and delivering high-quality solutions for patient safety
Job Summary
Verista empowers growth and innovation within the scientific community by solving business needs for life science industry leaders.
The company is seeking skilled QA Specialists to oversee compliance with cGMP, GDP, and other regulatory standards for facilities, equipment, processes, and documentation.
Verista offers exciting projects with leading pharmaceutical companies, competitive compensation, and opportunities for professional growth in a collaborative environment.
Matching Summary
Match Score: 85
Verista is seeking a Quality Assurance Specialist with over three years of experience in the pharmaceutical or biotech industries to join their team in Research Triangle Park, NC. The role focuses on ensuring compliance with regulatory standards and delivering high-quality solutions for patient safety.
Skills & Requirements
Must-have
cGMP compliance
GDP compliance
deviation management
CAPA management
change control
validation and audits
Nice-to-have
patient safety focus
regulatory compliance
team environment
innovative solutions
Key Requirements
3+ years in quality assurance
Pharmaceuticals or biotech experience
Based in or willing to relocate to Raleigh/Durham, NC