Roles & Responsibilities: Minimum of Six (6) years performing lifecycle computer-related systems validation in the biological manufacturing (GMP) industries. Computer Science bachelor's degree preferred. The equivalent combination of education/experience may be accepted in lieu of degree. Experience with computerized systems (e.g., Laboratory, LIMS, etc.). Experience with ERP systems (SAP, QMS (Veeva Vault), LIMS (MODO), PV Works). Support client site with computer-related systems validation activities. Work in a GMP environment in lifecycle documentation development, protocol execution and leading project efforts for computerized systems including laboratory, computer, and LIMS systems, etc. Supporting identifying Gaps in Lifecycle documentation and leading efforts to correct the Gaps. Support the CSV team to ensure they are achieving all identified goals and objectives. Katalyst Healthcares and Life Sciences
...better. We create fulfilling purpose-driven careers by learning from the world and each other. POSITION TITLE Senior Internal Auditor (SOX) POSITION LOCATION Richmond, VA YOUR ROLE You will serve as a member of the Genworth Corporate Audit...
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...Job Details Level Experienced Job Location Trenton Apartments I - Trenton, FL Position Type Full-Time (30 + hours/... ...: Under direct supervision of the Community Manager, the Maintenance Supervisor is responsible for the preservation and upkeep of...
...Job Description Production Operator \n Shift: 1st (7:00am-3:30pm) Monday-Friday \nPay: $17\n \nShift: 2nd (3p-1p30p)\nPay: $15.75\n\n Job Summary: \n\n Production operators tend machines such as automated assembly/robotic weld cells handling of metal...
...Duration: 12+ months Travel: Up to 25% Position Overview CereCore is seeking an EHR Project Manager to support and coordinate MEDITECH Expanse implementation projects. This role requires strong organizational skills, effective collaboration with stakeholders, and...