The position of Production Chemist I is within our Toxicology Business Unit located in California. Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. This job description will be reviewed periodically and is subject to change by management. RESPONSIBILITIES: * Adhere to laboratory safety rules * Read and understand Standard Operating Procedures (SOPs) related to job functions * Perform the daily, weekly, monthly, and yearly maintenance of laboratory equipment and maintain maintenance logbooks * Manufacture all products via Batch Records and/or Standard Operation Procedures (SOPs) following the guidelines for Good Manufacturing Practice (GMP) in accordance with the Quality System * Manufacture antibody solutions, drug positive solutions, enzyme-conjugate solutions, EIA calibrators and controls and reagents * Perform a variety of analytical EIA in-process testing * Perform daily temperature monitoring * Carry out production tasks in support of manufacturing goals and objectives * Participates in Lean Activities * Operate laboratory equipment safely, as trained and directed, in accordance with established practices * Maintain records and notebooks as directed in a neat, thorough and accurate manner. Perform required data entry on company planning and materials management system. Report results to supervisor * Maintain a neat and organized workplace. Ensure materials are appropriately labeled, approved for use and in enough quantity to complete required tasks * Recommend and participate in document revisions to ensure accurate BOM’s process descriptions * Recommend and participate in document revisions to ensure accurate NCMR and deviations * Perform complex simple formulations, component and material evaluations, equipment calibrations and maintenance * Ability to work overtime and/or on weekends * Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities * Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the companys policies and practices; build productive internal/external working relationships * Carries out duties in compliance with established business policies * Other duties as assigned, according to the changing needs of the business MINIMUM QUALIFICATIONS | EDUCATION/EXPERIENCE: * BA or BS in Chemistry or Biological Sciences * 0 to 2 years experience in laboratory environment * Strong verbal and written communication skills * Ability to follow detailed instructions, maintains accurate records and notes, and carries out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices PREFERRED QUALIFICATIONS: * Knowledge of a variety of lab equipment and their operation is preferred * Demonstrate problem-solving and troubleshooting skills * Process orientated, Logical, analytical, meticulous, highly organized and able to analyze data & implement solutions * Ability to work in a team environment while satisfying individual responsibilities and objectives. * Knowledge and ability to use MS Office and other manufacturing systems * Adaptable and willing to take on multiple new tasks and responsibilities * Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real time COMPETENCIES: * Attention to detail * Work in a team environment * Driven for results Pay ranges between 20-23/hr based on experience