The ideal candidate is highly organized, possesses strong attention to detail, and is comfortable working in a regulated production environment where accuracy and confidentiality are critical.

Key Responsibilities

• Participate in pre-production reviews with the Project Leader.
• Select and allocate appropriate label stock for production jobs.
• Prepare production rooms and workstations for area clearance.
• Print labels according to customer specifications and project requirements.
• Monitor printing operations to identify and address quality issues, defects, or production concerns.
• Perform reprint and integration activities for replacement labels as needed.
• Prepare packaging labels and supporting materials.
• Accurately document production activities and maintain required records throughout each run.
• Review production documentation for completeness and accuracy before submitting to Quality Assurance (QA) for review and release.
• Support shipping and fulfillment activities to meet customer requirements.
• Assist with additional operational tasks as needed to support day-to-day business operations.

Work Environment

CCL Clinical Systems is committed to providing a clean, safe, and professional work environment for all employees. This position requires working in a production setting where attention to detail, quality, and compliance are essential.

Confidentiality

Due to the nature of our business, all customer-related clinical trial information is strictly confidential. Employees are required to maintain confidentiality and adhere to company policies regarding the protection of customer and clinical trial data.