Night-Shift Packaging Lead | cGMP & Automation

Lonza; Tampa (FL); On-site; Confidential; Full time

Benefits offered by this job

Agile career culture

Inclusive workplace

Medical, dental, and vision insurance

Compensation programs recognizing high

Job summary

Lonza in Tampa, FL is seeking a Department Lead for Packaging to oversee night shift packaging operations and ensure compliant batch records and documentation. You will coordinate with Manufacturing, QA, Warehouse, and Facilities to ensure FDA alignment and high-quality outputs.

The role requires 4+ years in a GMP environment, strong cGMP knowledge, and the ability to lead staff, troubleshoot equipment, and support continuous improvement initiatives. A High School Diploma or GED is required.

Qualifications

• 4+ years of experience in manufacturing, packaging, or GMP-regulated environments.
• Strong understanding of cGMP requirements and documentation practices.
• Ability to lead others, troubleshoot equipment, and support cross-functional operations.

Responsibilities

• Lead Packaging operations, ensuring batch record execution and documentation meets cGMP standards.
• Coordinate with Manufacturing, QA, Warehouse, and Facilities teams to align with FDA and company requirements.
• Oversee cleaning and sanitization of packaging rooms and equipment.
• Assign and direct staff to production rooms to ensure smooth operations.
• Assist with troubleshooting equipment and set up automated packaging machinery.
• Reconcile and move materials between packaging areas and the warehouse.
• Train Operators and drive continuous improvement initiatives aligned with SQDC goals.

Skills

Leadership

cGMP knowledge

Troubleshooting

Documentation

Education

High School Diploma or GED

Tools

Packaging equipment

Job description

Lonza in Tampa, FL is seeking a Department Lead for Packaging to oversee night shift packaging operations and ensure compliant batch records and documentation. You will coordinate with Manufacturing, QA, Warehouse, and Facilities to ensure FDA alignment and high-quality outputs.

The role requires 4+ years in a GMP environment, strong cGMP knowledge, and the ability to lead staff, troubleshoot equipment, and support continuous improvement initiatives. A High School Diploma or GED is required.