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.
Requisitos:
•Doctor degree in Life Science or Engineering or Master’s degree in Life Science or Engineering and 3 years of Manufacturing or Quality in GMP regulated environment experience or Bachelor’s degree in Life Science or Engineering and 5 years of Manufacturing or Quality in GMP regulated environment experience.
•Project management skills
•Strong organizational skills, including ability to follow assignments through to completion
•Initiate and lead cross functional teams
•Enhanced skills in leading, influencing and negotiating
•Strong knowledge in area of expertise
•Collaborate and coordinate with higher level outside resources
•Strong knowledge of and experience with processes involved in manufacturing, QA, QC, validation and process development
•Demonstrate ability to interact with regulatory agencies
•Availability for 2nd and 3rd Shift