Onsite QMS Lead - Quality Systems & Compliance (Tampa)

Lonza Group Ltd.; Tampa (FL); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Bonus

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Matching

Life Insurance

Disability Insurance

Employee Assistance Program

Paid Time Off

Job summary

Lonza Group Ltd. in Tampa is seeking a QMS Administrator to strengthen enterprise quality systems and support digital transformation. This fully site-based role focuses on documentation, training, and audits to maintain high quality and safety standards in medicine manufacturing.

You will configure workflows, manage user access, and collaborate with Quality, IT, Manufacturing and Regulatory teams to drive continuous improvement while ensuring FDA and cGMP compliance.

Qualifications

• Bachelor's degree in Information Systems, Computer Science, Engineering or related field.
• 5+ years supporting enterprise systems or QMS in regulated environments.
• Experience with QMS platforms and FDA/cGMP requirements.
• Strong data analysis, configuration and workflow design skills.

Responsibilities

• Support implementation, administration and optimization of enterprise QMS for the Tampa site.
• Configure and maintain document lifecycle workflows, approvals, training and audits.
• Lead data migration activities including mapping, validation and reconciliation.
• Manage system users, roles and access per training/compliance requirements.
• Collaborate with Quality, IT, Manufacturing and Regulatory teams to drive improvements.
• Support testing, deployment, audits and inspections ensuring FDA and cGMP compliance.
• Develop SOPs, work instructions and quality metrics; mentor users on best practices.

Skills

System configuration

Troubleshooting

Data analysis

Workflow design

Education

Bachelor's Degree in Information Systems/ related field

Tools

Documentum

TrackWise

SharePoint

LIMS

Empower

Job description

Lonza Group Ltd. in Tampa is seeking a QMS Administrator to strengthen enterprise quality systems and support digital transformation. This fully site-based role focuses on documentation, training, and audits to maintain high quality and safety standards in medicine manufacturing.

You will configure workflows, manage user access, and collaborate with Quality, IT, Manufacturing and Regulatory teams to drive continuous improvement while ensuring FDA and cGMP compliance.