Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
September 15
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
• Lead, perform and report audits • Manage Technology audits • Lead and coordinate internal audit programs (global and regional) • Support Serious Breaches • Support Auditor Training and Mentoring • Maintain QA Records / Systems • Support Sponsor Audits and Regulatory Inspections • Maintain sound knowledge of Parexel policies, procedures, and guidelines and promote compliance within Parexel • Build, develop, and maintain working relationships with internal and external customer groups
• Strong knowledge of GxP, industry standards, applicable international technology compliance regulations • Must be detail oriented and able to maintain a ‘big picture’ overview during a sponsor audit or inspection • Ability to follow up on multiple tasks and projects, and to handle confidential information diplomatically • Familiar in technology as it relates to clinical trial activities, including System Life Cycle process and applicable GCP regulations pertaining to Computer Systems
Apply NowSeptember 15
501 - 1000
Ensure quality standards in robotic supply chain installations at Symbotic.
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Full-time QA Analyst ensuring data accuracy for cancer registry.
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💵 $50.9k - $72.2k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🔧 QA Engineer (Quality Assurance)
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🇺🇸 United States – Remote
💰 $30M Series C on 2022-02
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🟠 Senior
🔧 QA Engineer (Quality Assurance)