Supervisor, Microbiology

Lonza, Inc.•Greenwood, SC

61d•Onsite

About The Position

Based in Greenwood, SC, this role offers the opportunity to lead a dynamic microbiology lab team, driving quality and compliance in a fast-paced environment. What you'll get: An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits dependent on role and location The full list of our global benefits ca also be found on https://www.lonza.com/careers/benefits. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Requirements

A BA in biology or microbiology required (Master's or PhD preferred)
Proven experience in lab supervision and regulatory compliance
Strong communication and inclusive leadership skills
Ability to mentor and empower team members
Familiarity with CAPA, OOS investigations, and quality systems
Flexibility to work occasional weekends and holidays as needed
A commitment to ethical standards and continuous improvement

Responsibilities

Lead daily operations of the microbiology lab and perform routine testing when needed
Guide and support lab personnel and collaborate with site stakeholders
Ensure compliance with 21 CFR-Part 111 and 117 regulations
Drive investigations, issue deviations, and implement corrective actions
Oversee documentation, KPIs, and performance goals
Maintain and improve SOPs, protocols, and specifications
Contribute to audits and initiatives that enhance quality systems
Travel <10 %