Location: Tampa, FL
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join our Tampa site as a QA Specialist I, Compliance, where you will support document control and quality systems to ensure compliant GMP operations. This is an exciting opportunity to contribute to quality excellence and patient impact.
What you will get- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- Medical, dental, and vision insurance
- Opportunities for learning and career growth
- A collaborative and supportive team environment
- Access to global Lonza benefits programs
- Manage document control processes within the Quality Management System
- Review and approve GMP documents in a timely manner
- Maintain document archives and support inspection readiness
- Support internal audits, client audits, and regulatory inspections
- Track and manage document lifecycle activities and logs
- Collaborate with cross-functional teams to meet project goals
- Support deviation management, investigations, and change control
- Experience in a regulated environment, preferably pharmaceuticals
- Basic knowledge of GMP and FDA regulations
- Familiarity with QMS tools, or willingness to learn
- Strong written and verbal communication skills
- High attention to detail and organizational skills
- Ability to manage multiple tasks and deadlines
- High school diploma required; associate degree preferred
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.
Skills Required
- Experience in a regulated environment, preferably pharmaceuticals
- Basic knowledge of GMP and FDA regulations
- Familiarity with QMS tools, or willingness to learn
- Strong written and verbal communication skills
- High attention to detail and organizational skills
- Ability to manage multiple tasks and deadlines
- High school diploma required; associate degree preferred
What We Do
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.
