2nd-Shift Clinical Trial Materials Manager

IQVIA LLC; Marietta (GA); In loco; USD 77.700 - 161.800; Tempo pieno

Descrizione del lavoro

IQVIA Laboratories in Marietta, GA is seeking a Clinical Trial Material Manager (2nd Shift) to lead a 2:00 PM–11:00 PM manufacturing team in a regulated, high‑volume production environment, ensuring on-time delivery and quality compliance.

You will coach 20 direct reports, coordinate cross‑functional production activities with Project Management, Warehouse, Logistics, Quality and IT, and drive Lean and Six Sigma improvements to reduce bottlenecks.

Competenze

• Bachelor's degree or 10 years of experience in lieu of degree.
• Minimum 5 years of people management experience managing 20 employees.
• Minimum 5 years of experience leading manual assembly or production lines.
• Six Sigma Yellow or Green Belt; certification preferred.
• Proficiency with Excel, Outlook, and PowerPoint.

Mansioni

• Lead, coach, and develop a team of direct reports in a dynamic production environment.
• Manage daily and long-range production schedules to meet customer demand and service-level production targets.
• Prioritize urgent, same-day, and future-dated work orders to ensure on-time delivery.
• Coordinate daily with Project Management, Warehouse, Logistics, Quality, and IT to resolve production issues and prevent delays.
• Utilize LIMS to support production files, platform reports, production metrics, dashboards, and compliance reporting.
• Perform root cause investigations for quality incidents, customer complaints, operations incidents, and in-process deviations.
• Lead and support Lean, Six Sigma, and process improvement initiatives to optimize production flow and reduce bottlenecks.

Conoscenze

Leadership

People management

Process improvement

Six Sigma

LIMS

Communication

Manufacturing

Formazione

Bachelor's degree

Strumenti

Excel

Outlook

PowerPoint

LIMS

Descrizione del lavoro

IQVIA Laboratories in Marietta, GA is seeking a Clinical Trial Material Manager (2nd Shift) to lead a 2:00 PM–11:00 PM manufacturing team in a regulated, high‑volume production environment, ensuring on-time delivery and quality compliance.

You will coach 20 direct reports, coordinate cross‑functional production activities with Project Management, Warehouse, Logistics, Quality and IT, and drive Lean and Six Sigma improvements to reduce bottlenecks.