GMP Training Specialist - Night Shift

Lonza Inc.; Tampa (FL); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive compensation

Career growth opportunities

Collaborative work environment

Meaningful impact in life sciences

Ongoing training and learning

Exposure to quality systems

Global impact products

Job summary

Lonza Inc. in Tampa, FL is seeking a GMP Trainer for the 12-hour night shift to design and deliver training programs, support onboarding and qualification, and ensure training systems comply with regulatory and quality requirements.

You will collaborate with Operations, Quality and Safety to build a skilled workforce and maintain training records, SOPs, and assessments. Four years in manufacturing/training with pharma exposure is preferred.

Qualifications

• Experience creating training content, assessments, and development materials.
• Strong communication, presentation, and facilitation skills.
• Ability to maintain accurate documentation and training records.

Responsibilities

• Develop and maintain training materials, SOPs, on-the-job training programs, job aids, and assessments.
• Deliver classroom and hands-on training covering safety, GMP, GDP, equipment operation, and site procedures.
• Support onboarding, qualification, cross-training, and refresher training programs.
• Maintain accurate training records, qualification documentation, and training matrices.
• Partner with Safety, Quality, and Operations teams to ensure training meets business and compliance requirements.
• Identify skill gaps and implement training solutions to improve employee performance and effectiveness.
• Support training activities across multiple shifts as business needs require.

Skills

Training delivery

GMP knowledge

Documentation

Cross-functional collaboration

Communication skills

Education

High school diploma or GED

Job description

Lonza Inc. in Tampa, FL is seeking a GMP Trainer for the 12-hour night shift to design and deliver training programs, support onboarding and qualification, and ensure training systems comply with regulatory and quality requirements.

You will collaborate with Operations, Quality and Safety to build a skilled workforce and maintain training records, SOPs, and assessments. Four years in manufacturing/training with pharma exposure is preferred.