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Location: Salt Lake City, UT, United States
Position Type: Unfixed Term
Job Function: Bioscience R&D
At BioFire Diagnostics, LLC. we make the world a healthier place by providing molecular solutions that lessen the time to medical results and empower healthcare professionals to make better diagnostic decisions.
We are proud to be part of the bioMérieux family and the 5,000+ team members across 12 sites and subsidiaries in North America committed to our mission to help save lives around the globe through the power of diagnostics.
Come be a part of our team and our mission as a Laboratory Technologist I or II!
The schedule for this position will be Wednesday - Saturday 3:45 PM - 2:15 AM.
QC Technologist II works in a cGMP environment performing quality control testing for commercial and diagnostics products. Responsibilities include conducting testing of reagents and IVD materials as well as personnel swabs. Responsibilities include working with Manufacturing, Technology Transfer and other departments for data collections and validations for new product QC qualifications, organization of quality controlled materials used for QC testing and learning new techniques or workflow as required by new product lines.
QC Technologist II is also responsible for gathering and filling out quality documents pertaining to quality control testing, generation of Non Conformance Report (NCR) when necessary and Temporary Change Order (TCO) application. QC Technologist II will be responsible for software-assisted product release (e.g. Pouch QC Web releases).
This position will work in a laboratory setting and perform a variety of scientific techniques, including spectrophotometry, PCR, pipetting, etc.
Essential Job Duties and Responsibilities
Training and Education
Associate Degree or higher in a Life Science or related field.
Technologist I - Minimum 6 months previous experience in a laboratory setting (either academic or professional) is required.
Technologist II - Minimum of 2 years of experience in a laboratory setting or related area.
Experience in cGMP environment is strongly preferred.
Knowledge, Skills and Abilities