Quality Control Analyst

Johnson Matthey (‘JM’) is a global leader in science that enables a cleaner and healthier world. With over 200 years of sustained commitment to innovation and technological breakthroughs, we improve the function, performance and safety of our customers’ products. Our science has a global impact in areas such as low emission transport, pharmaceuticals, chemical processing and making the most efficient use of the planet’s natural resources. Today more than 14,000 Johnson Matthey professionals collaborate with our network of customers and partners to make a real difference to the world around us.

This position is responsible for performing routine analyses and support implementation of new analytical methods to the Quality Control Department.  The incumbent must exercise extreme care in laboratory work and keep detailed, clear, and accurate records of all laboratory work performed.

Key Responsibilities

•    Comply with all environmental & health and safety federal, state, local regulations and company policies.
•    Prepare chemical reagents and standards necessary for analyses.
•    Responsible for sample preparation and analyses of raw materials, in-process samples and finished product for physical properties and chemical constituents.
•    Perform non-routine analyses in support of QC functions as needed.
•    Implement methods and new procedures as needed.
•    Review analytical data for out of control conditions.
•    Maintain and troubleshoot instrumentation.
•    Maintain clear and accurate records. Revise and maintain quality documentation and procedures.
•    Train new employees in methods and procedures.
•    Ensures proper and effective communication of all issues.
•    Maintain a clean and safe work environment.
•    Be an effective trainer for new hires.

Are you the ideal candidate?

•    Bachelor’s Degree in Chemistry or related field
•    Knowledgeable in the areas of chemical analysis, quality systems, and manufacturing processes.  Familiarity with ICP or XRF analysis methods a plus.
•    Self-motivated and able to demonstrate the ability to work on an independent basis.
•    Working knowledge of Microsoft Office (i.e.: Excel, Word, & PowerPoint).
•    Good communication skills with ability to write detailed documentation and train Quality staff.
•    Capable of working as a team member with minimal supervision in a fast-paced environment.
•    Excellent organizational skills with emphasis on accuracy and detail.