Location: Rochester,NY, USA
The Quality Laboratory Analyst will provide technical support and assistance to the Quality Control and Assurance GMP laboratory at Eastman Kodak; involving chemical testing for in-process, WIP, & finished good products, raw materials & components and water samples; sampling of in-process products, WIP, finished good products, water samples, and raw materials & component receipts.
Specific Duties and Responsibilities:
Ability to maintain a GMP QC Laboratory notebook (hardcopy or electronic) adhering to Good Documentation Practices.
Perform instrumental and wet chemistry analytical tests on various materials and items.
Sampling of various materials.
Work in a GMP environment and comply with Quality Management System requirements.
Assist and perform in laboratory investigations.
Assist and perform in manufacturing investigations.
Assist and perform Corrective and Preventive Actions.
Assist and perform Non-conformance Reports.
Assist and perform facility inspections.
Assist and perform reports and presentations.
Maintaining QA Lab and QA instruments.
Coordinate Laboratory waste management.
Technical support and assistance as needed and assigned by supervision.
Excellent organizational and mathematical skills.
Qualifications (Education, Experiences and Skills):
Quality Control Chemist Bachelor's degree in Chemistry, Engineering, or related technical field AND 1-5 years of experience in a FDA/GMP regulated laboratory.
Or Laboratory Analyst Associates or Bachelor's degree in Chemistry, Engineering, or related technical field AND 0-3 years of experience in a FDA/GMP regulated laboratory.
Proficient in computer office platforms such as MS Office, MS Excel, MS PowerPoint, or related software.
Preferred experience with PH meter, balances, Osmolarity, Conductivity and other laboratory instruments.
Experience maintaining calibration and operation of analytical chemistry equipment.
Ability to follow instructions and SOPs.
Good documentation and communication skills.