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2nd Shift Pharmaceutical Manufacturing Operator (Packaging)

Job

Lonza Group Ltd

Tampa, FL (In Person)

$46,800 Salary, Full-Time

Posted 3 days ago (Updated 1 day ago) • Actively hiring

Expires 7/23/2026

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Job Description

Job Description Help for Job Description. Opens a new window. 2nd Shift Pharmaceutical Manufacturing Operator (Packaging) United States, Tampa (Florida) Posted Job Advert Packaging Operator Tampa, FL — Onsite 2nd shift available Lonza Tampa are looking for packaging operators with previous experience in GMP (Good Manufacturing Practices, i.e. Pharmaceutical, Medical Devices, Food, etc.) environments to work on our brand-new packaging and labelling processes within our capsule production lines. You will play a vital role in maintaining FDA-regulated standards, managing complex equipment, and ensuring 100% quality, directly supporting Lonza's mission to enhance lives worldwide. What you will get This full-time, hourly position is expected to offer compensation ranging from $21.00 - $24.00 per hour.
  • 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. Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge. 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.