Packaging Operator Hiring Event

Lonza•Tampa, FL

5d•Onsite

About The Position

Packaging Operator Tampa, FL — Onsite 2nd and 3rd shifts available Join Lonza Tampa as we implement brand‑new packaging and labeling processes that directly support our mission to enhance lives worldwide. This is an exciting opportunity to contribute to high‑impact operations while developing your skills in a dynamic, fast‑paced environment. What you will get An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Medical, dental and vision insurance. Opportunities to contribute to brand‑new packaging and labeling operations. What you will do Perform manual Primary and Secondary Packaging activities in alignment with batch record instructions. Operate and set up automated equipment to support packaging workflows. Ensure accurate reconciliation and movement of materials between packaging areas and the warehouse while maintaining strict chain of custody. Identify and report issues to QA, Team Leads, Equipment Specialists, CPS Project Coordinators, or Managers to prevent deviations. Support qualification and implementation of new equipment alongside the Equipment Specialist. Maintain up‑to‑date training and complete required logbook, SOP, and GMP documentation. Participate in production schedule meetings, project discussions, and safety processes to uphold world-class safety and quality standards. What we are looking for HS Diploma or equivalent experience. Experience working in a pharmaceutical GMP environment preferred. Familiarity with cleaning and sanitizing Primary and Secondary Packaging rooms. Ability to maintain professional, positive, and confidential interactions with sponsors and partners while adhering to regulatory requirements. Strong attention to detail and willingness to proactively stop work to ensure safety. Flexibility to take on additional duties as assigned. A collaborative mindset and commitment to high‑quality, compliant operations. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

Requirements

HS Diploma or equivalent experience.
Ability to maintain professional, positive, and confidential interactions with sponsors and partners while adhering to regulatory requirements.
Strong attention to detail and willingness to proactively stop work to ensure safety.
Flexibility to take on additional duties as assigned.
A collaborative mindset and commitment to high‑quality, compliant operations.

Nice To Haves

Experience working in a pharmaceutical GMP environment preferred.
Familiarity with cleaning and sanitizing Primary and Secondary Packaging rooms.

Responsibilities

Perform manual Primary and Secondary Packaging activities in alignment with batch record instructions.
Operate and set up automated equipment to support packaging workflows.
Ensure accurate reconciliation and movement of materials between packaging areas and the warehouse while maintaining strict chain of custody.
Identify and report issues to QA, Team Leads, Equipment Specialists, CPS Project Coordinators, or Managers to prevent deviations.
Support qualification and implementation of new equipment alongside the Equipment Specialist.
Maintain up‑to‑date training and complete required logbook, SOP, and GMP documentation.
Participate in production schedule meetings, project discussions, and safety processes to uphold world-class safety and quality standards.