Joulé
Sample Management Associate
Joulé, Sanford, North Carolina, United States, 27330
Job Title: Sample Management Associate
Considering making an application for this job Check all the details in this job description, and then click on Apply.Location: Sanford, NCType: ContractJoin the premiere pharmaceutical and biotechnology company that is in relentless pursuit of scientific breakthroughs and revolutionary medicines that will create a healthier world for everyone.
Responsibilities The position will support the Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, validation, and stability.Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; providing sample management support for QC; and creating, reviewing and approving documentation.Responsible for supporting the sample management process for QC (pick up from manufacturing, maintaining chain of custody in LIMS, aliquoting/delivering samples to appropriate lab, etc)
Requirements Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft Office™ applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs.FDA / GMP ComplianceGDP DocumentationLabware LIMSSample management and handling
Bioworks Certification with 2+ years of experience or Bachelor's
BenefitsSystem 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.
#M3
Considering making an application for this job Check all the details in this job description, and then click on Apply.Location: Sanford, NCType: ContractJoin the premiere pharmaceutical and biotechnology company that is in relentless pursuit of scientific breakthroughs and revolutionary medicines that will create a healthier world for everyone.
Responsibilities The position will support the Quality Operations department by performing Quality Control activities associated with clinical and/or commercial product, raw materials, validation, and stability.Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; providing sample management support for QC; and creating, reviewing and approving documentation.Responsible for supporting the sample management process for QC (pick up from manufacturing, maintaining chain of custody in LIMS, aliquoting/delivering samples to appropriate lab, etc)
Requirements Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft Office™ applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs.FDA / GMP ComplianceGDP DocumentationLabware LIMSSample management and handling
Bioworks Certification with 2+ years of experience or Bachelor's
BenefitsSystem 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.
#M3