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QA Specialist, Operations - 3rd shift

lonza

Tampa, FL

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JOB DETAILS
SKILLS
Biology, Biotech and Pharmaceutical, Compensation and Benefits, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Current Good Manufacturing Practice (cGMP), Dental Insurance, Detail Oriented, Documentation, Equal Employment Opportunity (EEO), GMP (Good Manufacturing Practices), Internal Audit, Maintain Compliance, Manufacturing Audit, Medical Products, Microsoft Office, Operational Support, Problem Solving Skills, Quality Assurance, Quality Assurance Methodology, Regulations, Regulatory Compliance, SAP, Safety Training, Safety/Work Safety, Standard Operating Procedures (SOP), Sustainability, Team Player, Vendor/Supplier Evaluation, Vision Plan
LOCATION
Tampa, FL
POSTED
Today
Job Title

QA Specialist, Operations - 3rd shift

Tampa, Florida, USA.

Join our Quality Assurance team in an entry-level role directly supporting operations You'll play a critical role in ensuring GMP compliance, documentation accuracy, and audit readiness across manufacturing. This is an exciting opportunity to gain hands-on experience while contributing to the quality and safety of products that impact millions of lives.

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.
  • Our full list of global benefits can be found here:
What you will do
  • Review SOPs, batch records, test methods, protocols, deviations, CAPA, and related documentation to ensure compliance with cGMP standards.
  • Approve SOPs, Master Batch Records, executed batch records, and laboratory data reports.
  • Assess product quality impact for open deviations during lot release.
  • Participate in investigations, audits (internal, vendor, customer), and provide support during regulatory inspections.
  • Collaborate with cross-functional teams to resolve issues and achieve departmental goals.
  • Attend client meetings and calls to support quality initiatives.
  • Ensure adherence to safety and sustainability requirements, reporting and correcting issues promptly.
What we are looking for
  • Bachelor's degree in a Science or related field required.
  • Entry-level candidates with foundational experience working in a cGMP-regulated pharmaceutical, biotech, or related environment.
  • Knowledge of Pharma cGMP standards required.
  • Familiarity with Trackwise, SAP, and Microsoft Office tools.
  • Strong attention to detail and ability to work collaboratively across teams.
  • Experience in audits and regulatory compliance processes is advantageous.


About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

About the Company

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lonza

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