# Clinical Trial Material (Kitting) 3rd Shift Supervisor

**Company**: IQVIA Laboratories
**Location**: Marietta, Georgia
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Salary**: $58,400.00 - $121,700.00
**Category**: Operations
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Clinical-Trial-Material--Kitting--Third-Shift-Supervisor_R1575752?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_4b577be0-b7c

## Description

We are seeking a Clinical Trial Material (Kitting) 3rd Shift Supervisor to join IQVIA Laboratories at Marietta, GA.

As a Clinical Trial Material (Kitting) 3rd Shift Supervisor, you will lead daily clinical trial material kitting operations in a regulated, high-volume production environment, ensuring on-time delivery, quality compliance, and strong team performance.

**Responsibilities**

- Lead, coach, train, and develop a team of approximately 15 direct reports

- Manage daily production schedules and prioritize urgent, same-day, future-dated, and business-critical work orders

- Serve as the first point of contact for production issues and escalate unresolved matters to CTM management

- Coordinate with Warehouse, Logistics, Quality, Project Services, and IT to prevent production delays and resolve operational issues

- Lead daily cross-functional meetings and communicate production priorities, risks, constraints, and performance updates

- Prepare production files and reports using LTMS, TOPCAT, QLIMS, Power BI, and other enterprise platforms

- Support root cause investigations involving quality incidents, customer complaints, operational incidents, and in-process deviations

- Ensure compliance with GMP, OSHA, SOP, training, and applicable regulatory requirements while supporting continuous improvement initiatives

**Requirements**

- An associate's degree or educational equivalent is required

- 3-4 years relevant experience including 1 year in a leadership capacity and/or equivalent combination of education, training and experience

- Working knowledge of Microsoft Excel, Outlook, and PowerPoint

- Experience using production, laboratory, or enterprise systems; familiarity with LTMS, TOPCAT, QLIMS, and Power BI is beneficial

- Working knowledge of applicable hazardous goods shipping regulations and regulated manufacturing requirements

**Knowledge, Skills and Abilities**

- Effective leadership, coaching, and team-development skills in a fast-paced production environment

- Excellent organizational skills, attention to detail, and the ability to manage competing priorities

- Strong written and verbal communication skills with a customer-focused approach

- Ability to establish and maintain effective working relationships with employees, managers, clients, and cross-functional partners

- Flexibility to work core third-shift hours of 11:00 p.m. to 6:00 a.m., with potential coverage from 2:00 p.m. to 11:00 p.m. based on business needs

- Flexibility to support overtime, weekends, and holidays when required by critical business needs and accelerated clinical trial timelines

**What We Offer**

- Competitive salary: $58,400.00 - $121,700.00 per year

- Comprehensive benefits program to support physical, mental and emotional, financial and social well-being

## Skills

### Required
- Microsoft Excel
- Outlook
- PowerPoint
- LTMS
- TOPCAT
- QLIMS
- Power BI
- GMP
- OSHA
- SOP

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marietta-Georgia-United-States-of-America/Clinical-Trial-Material--Kitting--Third-Shift-Supervisor_R1575752?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)