Team Lead, QA - 2nd Shift

Shift:3-11 M-F

Today, Lonza is a global leader in life sciences operating across three 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.

Elevate your career by joining Lonza AG as a Team Lead, QA - 2nd Shift in our Tampa, FL facility. This role is an outstanding opportunity to lead a team within a world-class manufacturing environment, ensuring flawless quality and compliance standards. If you are ambitious and ready to determine the future of manufacturing, this is the role for you!

• Ensure QA Operations personnel actively participate on the GMP manufacturing and packaging floor, offering support and mentorship during quality activities.

• Conduct detailed reviews of SOPs, batch records, test methods, and logbooks to ensure cGMP activities are meticulously completed and detailed.

• Write and approve SOPs and associated documentation independently.

• Approve Master Batch Records, customer audit, and regulatory CAPA.

• Ensure all QA activities align with company SOPs, cGMP standards, and FDA regulations.

• Assess the potential impact on product quality for open deviations during lot release.

• Participate in investigations into root causes, corrective or preventive actions, and impacts to product safety, identity, strength, quality, or purity.

• Recommend changes to processes and programs to successfully implement improvements.

• Guide, educate, nurture, supervise, and maintain a team of QA Operations personnel.

• Perform additional job-related assignments as requested by management.

• High school diploma or equivalent experience required; Bachelor’s degree or equivalent experience preferred.

• Proven experience in manufacturing operations, laboratory operations, and/or QA, preferably in pharma or biotech.

• 3+ years of relevant experience

Compensation for the role will depend on a number of factors, including the successful candidate’s qualifications, skills, competencies, experience, and job-related knowledge. Full-time employees receive a comprehensive benefits package including performance-related bonus, medical and dental coverage, 401k plan, life insurance, short-term and long-term disability insurance, an employee assistance program, paid time off (PTO), and more.

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.