QC Chemist I, GMP

Cayman Chemical•Ann Arbor, MI

3d•Onsite

About The Position

Cayman Chemical Company, headquartered in Ann Arbor, Michigan, is a supplier of resources for advancing human and animal health, offering a vast and growing product catalog and comprehensive service programs. Their mission is to make research possible by employing talented experts who develop tools to support research scientists. They are currently seeking to add a GMP QC Chemist I to their team.

Requirements

Bachelor's degree in Chemistry or related field.
1-3 years of laboratory experience using modern analytical instrumentation, including GC, HPLC, Karl Fischer, FT-IR, and related analytical techniques.
Proficiency in HPLC/GC analysis and participation in method development, validation, or transfer activities.
Ability to work normal business hours on-site in Ann Arbor, MI.
Demonstrate Cayman’s Core Values – Integrity, Collaboration, People, Learning, and Excellence.

Nice To Haves

Experience in a GMP-regulated environment is preferred.

Responsibilities

Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in-process samples, and finished APIs in accordance with approved specifications and procedures.
Assist with GC and HPLC method development, qualification, and optimization activities for new projects in compliance with GMP requirements.
Perform analytical testing to support method validation, transfer, verification, stability studies, and investigational activities (e.g., OOS/OOT), as well as other laboratory projects as assigned.
Promptly report all data aberrations to management and participate in supervised investigations.
Perform laboratory housekeeping, including glassware cleaning, reagent management, and routine instrument preventive maintenance activities.
Maintain complete, legible, accurate, and contemporaneous records of all laboratory activities in notebooks, logbooks, and electronic systems in compliance with GMP requirements and data integrity principles.
Perform secondary review of analytical data, calculations, and documentation generated by other analysts to ensure accuracy, completeness, and GMP compliance.
Communicate work status and progress to the supervisor on a regular basis.
Adhere to laboratory safety procedures and requirements, including proper handling of chemicals and hazardous materials.