Danaher
Quality Control Lab Technician III
Pensacola, Florida, United States · Mid
Sponsorship not specifiedDetected 7 hours ago
Data AnalysisStatisticsExcelAuditingProcess ImprovementGMPMedical DevicesResearchMass SpectrometryCommunicationProblem Solving
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Cap-exempt (no lottery)0
Sponsors this role78
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
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About the role
- 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.
Responsibilities
- Operate, calibrate, troubleshoot, and maintain laboratory instrumentation to ensure accurate and reliable results while documenting and reviewing data in compliance with GMP, GLP, GDP, ISO, and applicable regulatory standards.
- Investigate laboratory deviations and out-of-specification (OOS) results, support CAPA activities, and contribute to continuous improvement initiatives.
- Support method validation, verification, and transfer activities, including protocol execution, data collection, statistical analysis, and technical reporting.
- Perform analytical and laboratory testing using techniques such as Karl Fischer titration, Buchi IPA extraction, Gas Chromatography (GC), HPLC, Ion Chromatography (IC), FTIR, sample preparation, and data analysis in accordance with approved procedures and quality requirements.
- Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
Requirements
- Hands-on experience with analytical instrumentation, wet chemistry techniques, laboratory testing, and troubleshooting instruments.
- Strong analytical, organizational, and problem-solving skills with exceptional attention to detail and the ability to work independently.
- Effective written and verbal communication skills, including proficiency in Microsoft Excel and Word.
- Travel, Motor Vehicle Record & Physical/Environment Requirements Ability to travel up to 10%.
- Ability to stand for extended periods and lift, move, or carry equipment weighing up to 50 lbs.
- Experience writing and revising or auditing Quality Management System (QMS) documentation.
Nice to have
- It Would Be a Plus If You Also Possess Working knowledge of cGMP, GLP, GDP, ISO 17025, ISO 9001, ISO 13485, or similar quality management systems.
Compensation
- Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable.
Benefits
- Working at Cytiva means being at the forefront of providing new solutions to transform human health.
Company info
- 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.
- Manager, Laboratory Value Stream and is part of the Quality Department located in Pensacola, FL and will be an on-site role.
- At Cytiva we believe in designing a better, more sustainable workforce.
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This listing is sourced directly from Danaher's careers page and normalized into a canonical job model.