QC Batch Review Technician

Cytiva; Pensacola (FL); On-site; USD 42,000 - 65,000; Full time

Job summary

Cytiva in Pensacola, FL is seeking a QC Batch Review Technician to perform timely, accurate, and compliant review of raw material, intermediate, and finished good records to ensure ISO 9001 and Cytiva QMS compliance. This on-site role runs 11a–7p and supports product release with cross-functional collaboration.

The ideal candidate holds a Bachelor’s degree in Science or Engineering and 0–3 years of QA experience in ISO 9001 environments, with strong Excel data-tracking abilities for trend

Qualifications

• Bachelor’s degree in Science or Engineering required.
• 0–3 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.

Responsibilities

• 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.

Skills

Excel

Education

Bachelor’s degree in Science or Engineering

Job description

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

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.

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 working 11a to 7p.

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 required
• 0–3 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

Travel, Motor Vehicle Record & Physical/Environment Requirements

• Must have reliable transportation, and good driving record for travel between local sites if needed.
• Ability to lift, push, pull, or carry equipment up to 50lb
• Ability to perform tasks requiring fine motor skills and depth perception.

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.

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.

For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer.

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 [e-mail].