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Position Overview: We are seeking an individual to work as part of the Quality Control team. This individual will be responsible for analysis of raw materials and QC testing of in-process component and finished product. The QC testing of component and finished product will include performing manual and automated molecular assays and the use of specialized instruments. Key Responsibilities: Quality Control testing of in-process products, and finished products. Following Quality Control Procedures, adhering to QSR/GMP and all safety regulations as they apply to the laboratory and work areas. Maintain laboratory ingredients, chemicals, reagents, and relevant documentation as appropriate. Ancillary tasks will include ordering and stocking materials for formulation and maintaining and cleaning of equipment and laboratory space. Other duties and functions may be assigned to this position as needed.
Relocation costs may be covered.
Experience and Qualifications: Minimum BS degree in scientific discipline and 0-10 years experience in Biotech and/or IVD industry. Previous experience working under ISO or QSR/GMP guidelines for regulated molecular assays is a plus. Must be dependable, detail-oriented, and organized with the ability to follow instructions for formulations and QC testing. U.S. permanent residency required.
EMAIL cover letter & resume'.