Specialist Qa - Available To Work All Shifts

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.
*Other duties maybe assigned.*
Requisitos:
Education: Doctorate degree Master's degree and 3 years of directly related experience
Bachelor's degree in Science or Engineering and 5 years of directly related experience
Associate's degree and 10 years of directly related experience
High school diploma / GED and 12 years of directly related experience.
Science and Engineering

Preferred Qualifications:
Quality Professional with Manufacturing Process Audit and Batch Record Review experience.
In addition, some knowledge or to be familiar with DAI process, PASx/MES application, MAXIMO, SAP and LIMS.
Available for non-standard shift which includes nights and weekends.

Work Methodology:
100% On-site
2 years (1st contract)
Shift: 1st, 2nd and 3rd shift (Available for non-standard shift which includes nights and weekends.)
Professional Services Contract