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.