QA Specialist, Operations - 3rd shift

Join our team in Tampa, FL, where you’ll play a key role in ensuring compliance with cGMP standards and supporting quality assurance processes for manufacturing. This is an exciting opportunity to contribute to product quality and safety while collaborating across multiple departments. 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. 3+ years of relevant work experience in quality assurance or manufacturing required.{ #J-18808-Ljbffr Lonza Biologics Porriño SLU