HireTalent
Title: QC Support Analyst I
Location: 10210 Genetic Center Drive, San Diego, CA 92121
Duration: 6 months of contract
Shift Hours: This will be a first shift position that is expected to be the normal 40 hours/week. Associates are expected to start between 7 a.m. and 9 a.m., so the shift will end between 3:30 p.m. and 5:30 p.m.
Job Description: The Operations Test Associate candidate will be responsible for performing QC release testing and analysis of raw materials, in-process, and finished goods for the Molecular Diagnostics Division. The candidate will be responsible for understanding and executing testing on multiple assay platforms in a cGMP environment to ensure timely release of products.
Duties and Responsibilities:
Performs routine testing using GMP/GLP practices.
Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
Responsible for maintaining product and QC material inventories.
Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials.
Responsible for the maintenance and cleanliness of equipment, calibrating, or submitting items for calibration as needed.
Responsible for completing training in a timely manner and maintaining the records.
Participates in Laboratory Investigations for Invalid assays and Out-of-Specifications results.
Prepares documents for storage in our document management system and manages original data files.
Required Education: Bachelor’s degree in a science-related field
Key Requirements:
1 to 2 years of industrial lab experience (preferably QC)
Intermediate computer skills (i.e., Microsoft programs)
Working knowledge of industry/regulatory standards and GMP/GLP requirements
Preferred working knowledge of Enterprise Resource Planning (ERP), LIMS, and/or QSR
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Duration: 6 months of contract
Shift Hours: This will be a first shift position that is expected to be the normal 40 hours/week. Associates are expected to start between 7 a.m. and 9 a.m., so the shift will end between 3:30 p.m. and 5:30 p.m.
Job Description: The Operations Test Associate candidate will be responsible for performing QC release testing and analysis of raw materials, in-process, and finished goods for the Molecular Diagnostics Division. The candidate will be responsible for understanding and executing testing on multiple assay platforms in a cGMP environment to ensure timely release of products.
Duties and Responsibilities:
Performs routine testing using GMP/GLP practices.
Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
Responsible for maintaining product and QC material inventories.
Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials.
Responsible for the maintenance and cleanliness of equipment, calibrating, or submitting items for calibration as needed.
Responsible for completing training in a timely manner and maintaining the records.
Participates in Laboratory Investigations for Invalid assays and Out-of-Specifications results.
Prepares documents for storage in our document management system and manages original data files.
Required Education: Bachelor’s degree in a science-related field
Key Requirements:
1 to 2 years of industrial lab experience (preferably QC)
Intermediate computer skills (i.e., Microsoft programs)
Working knowledge of industry/regulatory standards and GMP/GLP requirements
Preferred working knowledge of Enterprise Resource Planning (ERP), LIMS, and/or QSR
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