Analytical Chemist (Chicago)

Summary

Our 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.

Responsibilities

• Perform 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.

Requirements

• Bachelor’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 & Start

• Onsite 5 days/week in Cary, IL
• 12+ month contract
• Start ASAP
• Benefits included (Medical, Dental, Vision)