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Verista

GxP lifecycle consulting for life sciences

Quality Assurance Specialists

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeResearch Triangle Park, Durham, NC, USANo salary listed

About the Job

Requirements

  • At least 3 years of quality assurance experience in the pharmaceutical or biotechnology industry.
  • Be based in or willing to relocate to Raleigh/Durham, North Carolina.
  • Oversee compliance with current Good Manufacturing Practices, Good Documentation Practices, and other regulatory standards for facilities, equipment, processes, and documentation.
  • Manage deviations, corrective and preventive actions, change control, validations, and audits.
  • Ensure production and testing records are accurate and complete.

About the Company

Verista

GxP lifecycle consulting for life sciences

Verista provides business and technology consulting for life science companies, focusing on systems, compliance, validation and quality across the GxP lifecycle. Its services cover preclinical, clinical, commercialization, manufacturing and distribution to ensure safe, high-quality results. The company combines decades of industry knowledge with advanced engagement platforms and transformative technologies to help clients solve complex challenges with one partner across specialties. With a team of 500+ experts, Verista supports clients from strategy and validation to execution, delivering consistent, compliant outcomes that improve health and lives. The goal is to enable better health outcomes by ensuring products and processes are safe, compliant and efficient throughout the product development lifecycle.

Company size
201-500
Company stage
Not listed
Total funding
Not listed
Headquarters
Fishers, IN
Founded
2020

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