Overview
Technical Writer, Quality Assurance Jobs in Sylmar, CA at Abbott Laboratories
Quality Professional with experience in Quality Systems management (Deviations, CAPAs, Change Controls), Equipment, Processes and Facilities Validation.
Functions:
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.
Designed 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.
Requirements:
Doctorate degree or Master’s degree and 3 years of directly related experience Bachelor’s degree and 5 years of directly related experienceAssociate’s degree and 10 years of directly related experienceHigh school diploma / GED and 12 years of directly related experience.
Knowledge or to be familiar with in PASx/MES application, MAXIMO, SAP, LIMS, QMTS and Veeva.
Experience in Quality Systems (Deviations, CAPAs, Change Controls) and Equipment, Processes and Facilities Validation
Available during weekends and holidays as requested.
Bilingual (Spanish/English)
Technical Writing
Job Types: Full-time, Contract
Education:
Bachelor’s (Preferred)
Experience:
Quality systems: 5 years (Preferred)
Facilities Validation: 5 years (Preferred)
Processes: 5 years (Preferred)
Equipment: 5 years (Preferred)
Language:
Spanish (Preferred)
English (Preferred)
Work Location: In person
Title: Technical Writer, Quality Assurance
Company: Abbott Laboratories
Location: Sylmar, CA
