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 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. 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 customers undertake life‑saving activities ranging from fundamental biological research to developing innovative vaccines, 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.

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.

• 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; maintain release logs and support internal audits.

• 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.

• Ability to lift, move or carry equipment up to 50 lbs.

• Previous experience in Quality Assurance or Quality Control in a GLP/GMP/ISO 9001 company, preferably in the biotechnology/pharmaceutical industry.
• Build and utilize strong working relationships with other departments.

Cytiva offers a comprehensive benefits package that includes medical, dental, vision insurance, paid time off, and a 401(k) plan. This position is eligible for bonus and incentive pay.

This role is eligible for a remote work arrangement—a remote work option may be provided with additional information during the interview process.

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.

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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