Analytical Chemist II

Analytical Chemist II

Working at Abbott

The Opportunity

Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.

The position of Analytical Chemist II is within our Toxicology business unit located in Pomona, California. This role performs qualitative and quantitative analyses of compounds in biological samples; conducts measurements of in-process and final product; conducts research to develop or improve analytical techniques, methodology, procedures, and investigates application of instruments in analysis.

What You’ll Work On

• Performs quantitative analytical testing using potentially complex methods, procedures and equipment.

• Generate analysis reports. Provides quality control specifications to ensure process consistency, quality and optimal yield performance.

• Perform the daily, weekly, monthly, and yearly maintenance of laboratory equipment and maintain maintenance logbooks.

• LC-MS/MS and GC-MS operator.

• Extraction chemist for multiple matrices.

• Troubleshoot instruments and lab equipment.

• Assist with quality control and quality assurance practices.

• Assist with SOP updates and modifications.

• Participate in proficiency testing.

• Establish or revise procedures.

• Provide training and development of newly hired personnel on all the different aspects of testing and laboratory maintenance.

• Maintain a neat and organized workplace. Ensure materials are appropriately labeled, approved for use and in enough quantity to complete required tasks.

• Works independently using discretion and best judgment while coordinating work efforts with other colleagues.

• Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.

• 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.

• Carries out duties in compliance with established business policies.

• Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.

• Perform other duties & projects as assigned.

Required Qualifications

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