Manager, Microbiology

Lonza•Tampa, FL

1d•Onsite

About The Position

Join our Tampa site as a Microbiology Manager, where you’ll lead a high‑impact QC Microbiology function supporting development, clinical, and commercial programs. This is an exciting opportunity to guide scientific strategy, mentor microbiology professionals, and influence product quality for therapies that improve patient lives. Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

Requirements

Bachelor’s or Master’s degree in Microbiology, Biology, or a related field required (advanced degree preferred).
Extensive experience in microbiology including leadership or supervisory experience in a cGMP environment.
Strong technical knowledge in microbiological techniques, aseptic practices, environmental monitoring, method validation, and data trending.
Demonstrated ability to lead teams, influence cross‑functional partners, and support operational excellence in a fast‑paced setting.
Strong problem‑solving skills with experience conducting root‑cause analysis and implementing effective CAPAs.
Ability to manage multiple priorities while ensuring compliance with FDA, EMA, ICH, USP, ISO, and 21 CFR 210/211 guidelines.

Nice To Haves

Familiarity with LIMS systems, digital lab management tools, and risk‑assessment methodologies is a plus.

Responsibilities

Lead day‑to‑day operations of the QC Microbiology laboratory, ensuring accurate, timely, and compliant testing across development, clinical, and commercial programs.
Provide leadership, coaching, and development for microbiologists and lab technicians while fostering a culture of quality and continuous improvement.
Oversee key programs including environmental monitoring, sterility assurance, microbial identification, and method development/validation.
Collaborate closely with Quality Assurance, Production, R&D, and client teams to resolve microbiological challenges and support product and process development.
Review and approve test data, investigations, SOPs, protocols, and technical reports in alignment with cGMP and global regulatory requirements.
Manage QMS/TrackWise records including deviations, CAPAs, change controls, and microbiology‑related investigations.
Prepare for and participate in internal and external audits, and monitor laboratory metrics to drive performance improvements.