Joulé
QC Analyst
Joulé, Orangeburg, New York, United States, 10962
Job Title: QC Analyst
Please read the following job description thoroughly to ensure you are the right fit for this role before applying. Location: Orangeburg, NY area Hours: 2nd Shift (2:00pm-10:30pm) Type: 6 month contract to start
Responsibilities:
Performs analyses of Clinical Chemistry, Critical Care, coagulation and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product Interprets test results against specifications and decides if assays pass or fail Maintains documentation of all work performed in accordance with GMP requirements Performs product stability, proficiency, environmental testing and water system testing Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of lab equipment Updates departmental SOP's and QC Monographs as directed Performs microbial testing per SOP's and QC Monographs Orders required laboratory supplies, reagents and other consumables Monitors proper storage conditions and expiration dates Disposal of hazardous and bio-hazardous materials Maintains retain samples in accordance with established procedures Maintains statistical process control charts and other tracking reports
Requirements: BS/BA Biology, Chemistry, or Medical Technology Minimum 3-6 months of research experience (could be academic, internship, co-op) or industry experience
Benefits
System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan
Please read the following job description thoroughly to ensure you are the right fit for this role before applying. Location: Orangeburg, NY area Hours: 2nd Shift (2:00pm-10:30pm) Type: 6 month contract to start
Responsibilities:
Performs analyses of Clinical Chemistry, Critical Care, coagulation and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product Interprets test results against specifications and decides if assays pass or fail Maintains documentation of all work performed in accordance with GMP requirements Performs product stability, proficiency, environmental testing and water system testing Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of lab equipment Updates departmental SOP's and QC Monographs as directed Performs microbial testing per SOP's and QC Monographs Orders required laboratory supplies, reagents and other consumables Monitors proper storage conditions and expiration dates Disposal of hazardous and bio-hazardous materials Maintains retain samples in accordance with established procedures Maintains statistical process control charts and other tracking reports
Requirements: BS/BA Biology, Chemistry, or Medical Technology Minimum 3-6 months of research experience (could be academic, internship, co-op) or industry experience
Benefits
System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan