GMP Audit Lead — Quality & Compliance Leader

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

Job summary

Lonza in Tampa, FL seeks a Lead Auditing QA Specialist to oversee audit programs ensuring GMP compliance across products and processes. You will lead audits, draft findings, and drive corrective actions, collaborating with cross-functional teams to sustain quality and regulatory adherence.

The role demands strong leadership, 5+ years in pharma QA, and excellent communication to coordinate with internal teams and external partners. On-site position based in Tampa, Florida.

Qualifications

• Bachelor's degree in a science field and 5+ years in pharma/manufacturing QA.
• Strong understanding of GMP regulations and quality systems.
• Excellent written and verbal communication skills with internal/external stakeholders.

Responsibilities

• Lead audits of products and processes to ensure compliance with industry regulations and company standards.
• Conduct opening and closing meetings, draft objectives and audit reports, determine final compliance conclusions.
• Develop audit plans detailing objectives, scope, criteria and schedule.
• Select an audit team based on audit complexity and required expertise.
• Ensure audits are conducted within timelines and resources are allocated efficiently.
• Represent the company in external audits and inspections.

Skills

GMP knowledge

Audit leadership

Communication

Organizational skills

Education

Bachelor's degree, science preferred

Job description

Lonza in Tampa, FL seeks a Lead Auditing QA Specialist to oversee audit programs ensuring GMP compliance across products and processes. You will lead audits, draft findings, and drive corrective actions, collaborating with cross-functional teams to sustain quality and regulatory adherence.

The role demands strong leadership, 5+ years in pharma QA, and excellent communication to coordinate with internal teams and external partners. On-site position based in Tampa, Florida.