This is a first shift position (8:00am - 5:00pm). Will require occasional work during the other shifts when support is needed.
To support process engineers with new product development and process improvements for existing products.
As a mid-level technician in R&D, will provide support to process engineers in developing processes and assisting in pilot scale and full scale batch manufacture for sterile solution, suspension and ointment products. Additionally, will also support process and cleaning validations.
The position will also provide support generating laboratory controls for QC Chemistry and Microbiology as well as maintain the pilot lab and pilot equipment.
This person will Comply with company cGMP and safety practices and procedures, including, participating in GMP training, and fulfilling aseptic training requirements.
High school diploma, Associates degree preferred in one of the physical sciences. Specialized training and relevant on the job or certification will be considered.
Must have a strong work ethic and good attention to detail, and be able to work independently.
Computer literate, and is able to use Microsoft Office software (Word, XL, etc.)
Desired: Previous experience working in a sterile manufacturing environment.
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Valeant Pharmaceuticals International, Inc. is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.