Analytical Chemist

SummaryOur client, a Fortune 500 medical device company, is seeking an Analytical Chemist to support the Product Development R&D team in Cary, IL. The team has recently established in-house chemistry and microbiology lab capabilities, and this role will focus on executing analytical testing, supporting method development, and ensuring high-quality, compliant laboratory operations.The Analytical Chemist will work within a regulated environment to support routine testing, developmental studies, and stability programs while adhering to GMP/GLP standards.ResponsibilitiesPerform routine and non-routine analytical testing to support R&D product development and stability studies.Assist in method development, verification, and validation activities under the guidance of senior staff.Follow established lab processes, workflows, and SOPs to ensure accurate and compliant data generation.Prepare samples, reagents, and standards in accordance with documented procedures.Operate and maintain analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR), including basic troubleshooting.Support calibration, preventive maintenance, and documentation for laboratory equipment.Accurately document experimental data, observations, and results in compliance with data integrity standards.Assist in reviewing data for accuracy, completeness, and compliance with GMP/GLP requirements.Participate in lab investigations, deviations, and root cause analyses as needed.Maintain proper lab organization, material segregation, and safety practices.Collaborate with cross-functional R&D team members to support project timelines and deliverables.Contribute to continuous improvement initiatives to enhance lab efficiency and reliability.RequirementsBachelor's degree in Chemistry or a related scientific discipline (Master's preferred but not required).5+ years of experience in an analytical chemistry laboratory, within an FDA-regulated (GMP/GLP) environment.Hands-on experience with common analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR).Familiarity with method development and validation concepts is preferred.Understanding of basic laboratory compliance, documentation practices, and data integrity principles.Experience in the pharmaceutical industry required.Strong attention to detail and ability to follow established procedures.Ability to work independently as well as part of a team in a fast-paced R&D environment.Basic knowledge of instrument calibration and maintenance practices.Experience with microbiology techniques is a plus but not required.Terms & StartOnsite 5 days/week in Cary, IL12+ month contractStart ASAPBenefits included (Medical, Dental, Vision)

Created: 2026-05-09