Quality Control Lab Technician

What You Will Do

• 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. Analyze and trend laboratory data using Microsoft Excel and communicate results through clear technical documentation and reports.
• 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.
• Who You Are
• Bachelor’s degree in Chemistry, Biology, or a related scientific discipline with 3+ years of laboratory experience- preferably, in a regulated environment (e.g., pharmaceutical, medical device, manufacturing, food, environmental, or quality testing).
• 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. Passionate about improving human health and committed to learning, innovation, and continuous improvement, including the effective use of digital and AI-enabled tools.
• 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.
• 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.
• Experience writing and revising or auditing Quality Management System (QMS) documentation.
• Lean, Six Sigma, or other continuous improvement training or certification.
• 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.
• 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.
• 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 please click 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 [email protected].