Clinical Trial Materials Team Lead - 3rd Shift

IQVIA Inc; Marietta (GA); On-site; USD 58,000 - 122,000; Full time

Job summary

IQVIA Laboratories in Marietta, GA is seeking a Clinical Trial Material (Kitting) 3rd Shift Supervisor to lead daily production in a regulated, high- volume environment and collaborate across Project Services, Warehouse, Logistics, Quality and IT.

You will manage a team of about 15 direct reports, schedule work orders, address production risks, support quality investigations, ensure GMP compliance, and drive continuous improvement while working the 11:00 p.m.–6:00 a.m.

Qualifications

• Associate's degree or educational equivalent is required.
• 3–4 years relevant experience including at least 1 year in a leadership role.
• Working knowledge of Microsoft Excel, Outlook, and PowerPoint.
• Experience with LTMS, TOPCAT, QLIMS, and Power BI is beneficial.
• Hazardous goods shipping regulations and regulated manufacturing requirements familiarity.

Responsibilities

• Lead, coach, train, and develop a team of ~15 direct reports.
• Manage daily production schedules and prioritize urgent work.
• Serve as first contact for production issues and escalation to CTM management.
• Coordinate with Warehouse, Logistics, Quality, Project Services, and IT.
• Lead daily cross-functional meetings and communicate priorities and risks.
• Prepare production files and reports using LTMS, TOPCAT, QLIMS, and Power BI.
• Support root-cause investigations involving quality incidents and deviations.
• Ensure GMP/OSHA/SOP compliance and support continuous improvement.

Skills

Leadership

Team coaching

Microsoft Excel

PowerPoint

Power BI

LTMS

TOPCAT

QLIMS

Cross-functional collaboration

Education

Associate degree or equivalent

Tools

LTMS

TOPCAT

QLIMS

Power BI

Job description

IQVIA Laboratories in Marietta, GA is seeking a Clinical Trial Material (Kitting) 3rd Shift Supervisor to lead daily production in a regulated, high- volume environment and collaborate across Project Services, Warehouse, Logistics, Quality and IT.

You will manage a team of about 15 direct reports, schedule work orders, address production risks, support quality investigations, ensure GMP compliance, and drive continuous improvement while working the 11:00 p.m.–6:00 a.m.