QC Batch Review Technician

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The QC Batch Review Technician is responsible for timely, accurate and compliant review of raw material, intermediate and finished good records to ensure compliance with ISO 9001 and Cytiva QMS standards. Supports timely product release by resolving documentation issues and coordinating with Production & Supply chain to drive cross-functional cooperation and improvements. Collects raw material samples, performs basic product testing and supports compliance audits at GEMBA. This position reports to the Quality Value Stream Manager and is part of the Quality Department located in Pensacola, FL and will be an on-site role.

What you will do:

Conduct raw material incoming inspection activities as well as finished batch release activities in compliance with

ISO 9001

& Cytiva QMS. Verify adherence to GDP, perform sample collection, complete testing, and verify documentation meets requirements Initiate nonconformance records, own block/release stock activities and where appropriate, participate in nonconformance investigations and Maintain release logs and support internal audits.

Who you are:

Bachelor's degree in Science or Engineering preferred; no previous experience required, though 1-3 years of QA experience in an ISO 9001-regulated environment is a plus Ability and willingness to become proficient in tracking and trending data in Excel; capable of managing simultaneous assignments while maintaining strong attention to detail Ability to perform tasks requiring fine motor skills and depth perception, including lifting, pushing, or pulling up to 50 lbs.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

Ability to lift, move or carry equipment up to 50lb It would be a plus if you also possess previous experience in: Quality Assurance or Quality Control in

GLP/GMP/ISO 9001

company preferably in the biotechnology/pharmaceutical industry. Build and utilize strong working relationships with other departments Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note:

No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The

U.S. EEO

posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com. Danaher is a leading global life sciences, biotechnology, and diagnostics innovator, helping to solve many of the world's most important health challenges, ultimately improving quality of life for billions of people today, while setting the foundation for a healthier, more sustainable tomorrow. The Danaher ecosystem is made up of more than 15 businesses united by a shared commitment to innovate for tangible impact. Please read our Applicant Data Privacy Notice carefully here.