Valeant Pharmaceuticals International, Inc. is a multi-national specialty pharmaceutical company focused on developing prescription and non-prescription pharmaceutical products designed to make a meaningful difference in patients' lives.
Reporting to the Quality Control Supervisor, you will be responsible performing a variety of Quality Control testing with results meeting cGMP requirements. Duties include participating in routine sample testing such as raw material, finished products, in-process, stability, cleaning validation, purified water, and environmental sampling using established analytical procedures and wet chemistry techniques As part of the team you will operate and maintain various lab instrumentation such as analytical scale, FTIR, HPLC, Karl Fischer, GC and dissolution apparatus. You will recognize out-of-specification or out-of-trend results and assist in the completion of lab investigation.
The successful applicant will have College diploma in Chemical Technology or Bachelor’s degree in Chemistry or Life Sciences or related studies and/or equivalent combination of education and experience is required. You will have working knowledge of GMP's, MS Office, as well proficiency with laboratory instrumentation.
We offer a challenging, team-oriented work environment, competitive compensation and benefits as well as opportunities for professional growth and development.