Specialist Qa – (30294)

Descripción del Empleo:
Perform one or more of the following duties and responsibilities in support of client’s Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team. Approve Environmental Characterization reports. Release of sanitary utility systems. Approve planned incidents. Represent QA on NPI team. Lead investigations. Lead site audits. Own site quality program procedures. Designee for QA manager on local CCRB. Review Risk Assessments. Support Automation activities. Support facilities and environmental programs. Review and approve Work Orders. Review and approve EMS/BMS alarms. Approve NC investigations and CAPA records. Approve change controls. Provide lot disposition and authorize lots for shipment.

COMPETENCIES/SKILLS Project management skills, Strong orga
Requisitos:
Doctorate degree or Master’s degree and 3 years of directly related experience or Bachelor’s degree and 5 years of directly related experience
Natural Science-related background (e.g., Chemistry, Biology, Microbiology, etc.)

Support various Transfer/Incoming/Validation activities across various areas such as Incoming/QC/Process Development/Facilities so experience in Qualification/Validation activities is a must.
Experience on the following:
• Quality Assurance (QA), Quality Control (QC), or Incoming. Preferably in QA
• Deviations, Data integrity, Validation, Work Orders (WO), Equipment Alarms, Compliance, Investigations, Technical Support, or Regulatory reviewing and approving records.
Highly Desirable:
• Experience with managing records in Trackwise, review and approval of validation records and documentation
• Experience in Change Control and managing Deviations
Administrative Shift