Night Shift Packaging Supervisor — Lead cGMP Team

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

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Inclusive Workplace

Performance-based pay

Process improvement opportunity

Job summary

Lonza Tampa is seeking a Packaging Supervisor to lead daily operations within the packaging department, ensuring safe, compliant, and efficient production. This role offers the opportunity to influence manufacturing excellence and mentor a growing team.

The ideal candidate has 6+ years in a cGMP pharmaceutical environment, strong leadership and data/documentation skills, and the ability to collaborate with QA, PM, and operations teams. On-site role in Tampa, FL with comprehensive benefits.

Qualifications

• Minimum 6 years in a cGMP pharmaceutical manufacturing environment.
• Proven leadership capabilities with experience supervising or directing teams.
• Strong understanding of good manufacturing practices and regulatory requirements.
• Excellent communication, problem-solving, and documentation abilities.
• Ability to collaborate effectively with QA, Project Management, and operations teams.

Responsibilities

• Lead, coach, and direct packaging team members to ensure alignment with procedures, processes, and cGMP expectations.
• Manage day-to-day operations and maintenance of the packaging facility to uphold production efficiency.
• Review production schedules and collaborate with the Master Scheduler to support accurate documentation and timely issue resolution.
• Conduct and close quality event investigations, ensuring strong compliance and documentation practices.
• Hire, mentor, and develop employees to build a skilled, engaged packaging team.
• Deliver hands-on technical and cGMP training directly on the shop floor.
• Coordinate indirect material purchases and manage overtime to meet operational needs.

Job description

Lonza Tampa is seeking a Packaging Supervisor to lead daily operations within the packaging department, ensuring safe, compliant, and efficient production. This role offers the opportunity to influence manufacturing excellence and mentor a growing team.

The ideal candidate has 6+ years in a cGMP pharmaceutical environment, strong leadership and data/documentation skills, and the ability to collaborate with QA, PM, and operations teams. On-site role in Tampa, FL with comprehensive benefits.