Quality Control Lab Technician III

About the role

This position reports to the Sr. Manager, Laboratory Value Stream and is part of the Quality Department located in Pensacola, FL. It is an on-site role focused on conducting routine and non-routine analysis of raw materials, in-process, and finished goods, maintaining quality metrics, and supporting the QA laboratory.

Responsibilities

• 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.

Requirements

• 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, Physical & Environmental Requirements

• Ability to travel up to 10%.
• Ability to stand for extended periods and lift, move, or carry equipment weighing up to 50 lbs.

Preferred Qualifications

• 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.

Benefits

Cytiva offers a broad array of comprehensive, competitive benefit programs, including:

• Paid time off.
• Medical, dental, and vision insurance.
• 401(k) retirement plan.
• Bonus/incentive pay eligibility.

For more details, visit Danaher Benefits Info.

Work Arrangement

This position is eligible for a remote work arrangement, allowing you to work remotely from your home. Additional details about this arrangement will be provided during the interview process.