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Job Requirements of Operations Test Associate:
-
Employment Type:
Contractor
-
Location:
San Diego, CA (Onsite)
Do you meet the requirements for this job?
Operations Test Associate
Careers Integrated Resources Inc
San Diego, CA (Onsite)
Contractor
INTAKE NOTES;
Pay Range: *** ***/hour
Status: Onsite
Proposed start date: ASAP
Goal: To extend, though there are no guarantees for conversion
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.
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
Role: 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: The incumbent may be asked to perform other function-related activities in addition to the responsibilities mentioned below as reasonably required by business needs.
Performs routine testing using GMP/GLP practices.
Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
May perform microbiology testing and activities for the QC Micro team.
May perform pH and/or HPLC testing for the QC Analytical team.
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.
Pay Range: *** ***/hour
Status: Onsite
Proposed start date: ASAP
Goal: To extend, though there are no guarantees for conversion
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.
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
Role: 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: The incumbent may be asked to perform other function-related activities in addition to the responsibilities mentioned below as reasonably required by business needs.
Performs routine testing using GMP/GLP practices.
Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
May perform microbiology testing and activities for the QC Micro team.
May perform pH and/or HPLC testing for the QC Analytical team.
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.
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