Clinical Trial Material Manager (2nd Shift)

$77.7k - $161.8k

IQVIA

IQVIA seeks a Clinical Trial Material Manager for second-shift operations at its Marietta laboratory. The role oversees daily manufacturing of clinical trial materials in a regulated, high-volume environment, managing teams, production schedules, quality compliance, and process improvements across multiple departments.

Responsibilities

Lead and develop direct report team in second-shift production operations
Manage daily and long-range production schedules to meet customer demand targets
Prioritize work orders to ensure on-time delivery and resolve production delays
Conduct root cause investigations for quality incidents and process deviations
Support Lean and Six Sigma process improvement initiatives to optimize production

Requirements

Bachelor's degree or 10 years manufacturing experience
Minimum 5 years managing 20+ employees in manufacturing
Minimum 5 years managing manual assembly or production lines
Minimum 2 years leading process improvement projects
Six Sigma Yellow or Green Belt certification
Working knowledge of ICH, GMP, and OSHA regulations
Proficiency with Microsoft Excel, Outlook, and PowerPoint

Compensation: $77,700-$161,800 base annually

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Vacancy posted 5 days ago

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