Quality Control Lab Technician

Danaher • Pensacola, FL

8d • Onsite

About The Position

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 Lab Technician is responsible for conducting routine and non-routine analysis of raw materials, in-process, and finished goods, creating and maintaining databases to ensure consistent quality metrics and maintaining the QA laboratory . This position reports to the QA Manager and is part of the Quality Assurance Department located in Pensacola, FL and will be an on-site role.

Requirements

• BS in Life Sciences with 1 year Quality experience.
• Ability to perform tasks requiring fine motor skills and depth perception
• Ability to complete work on time doing simultaneous assignments while maintaining proper attention to detail
• Ability to lift, move or carry equipment up to 50lb

Nice To Haves

• Using GC, HPLC, Microplate readers, cell cultures.
• Karl Fisher, Ion Chromatography, Soxhlet Extraction, and liquid particle counters
• 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

Responsibilities

• Perform and analyze a variety of QC tests according to Standard Operating Procedures and accurately document results via established product specifications.
• Analyze, interpret, report and review test results on the internal Database system
• Identify non conformances and Out of Specification results, initiate and perform Out Of Specification Investigations.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level