Unilever Quality Process Auditor 1 in Manila, Philippines
Quality Process Auditor 1
Conducts cGMP monitoring and audit of all production facilities, machines, excess materials (RM/PM), and personnel (regular and contractual) before and after production or as needed to ensure implementation and compliance to Unilever GMP standard
Discusses results of audit / monitoring with concerned Supervisor and recommends action points. Conducts follow up on compliance to committed action plans and timetable.
Conducts random sampling for raw and packaging materials being used for production.
Conducts physico-chem analysis of process water/ semi-finished goods and encodes results in the system for timely filling/ packing of every batch tank preparation.
Troubleshoots all noted exceptions during monitoring or physico-chem analysis and recommends actions to be done to avoid line rejections.
Ensures that all mixes produced comply with the standard quality parameters set by R&D group through process monitoring, micro and cut-out sampling. Conducts visual and sensorial inspection and encodes in the system results of evaluation for timely finished goods release.
Temporarily puts on hold affected lots and validate noted problem / exception. Documents all exceptions noted and conducts investigation to get details of reported problems. Monitors status of the affected products / materials and gives update to immediate superior.
Ensures compliance of operators to HACCP plans by making sure that product quality monitoring (PQM) of all work-in process operations in production is properly accomplished. Recommends revision in HACCP plan based on production quality performance.
Verification of End of Line Quality Parameters and CCP. Eg. Sensors and Check Weigher verification
Attends / assists to batch trial run (BTR) meetings and monitoring
Conducts analysis of results of 20 commercial runs (including the first five commercial runs monitored by R&D) to qualify product for Auto Release status.
Encodes, reviews and analyzes all data gathered during process monitoring (SPC encoding/ CRQS monitoring for shopfloor & ex-factory), QCP’s / CCP’s monitoring, including line exceptions as documented through CPAR and QBO for specifications update, process and line quality improvements.
Conducts evaluation of and provides disposition on affected finished products.
Ensures good housekeeping of all materials being used and the work area at all times
Conducts review and control of all documents received from other departments.
Performs inventory and control of inspection gadgets, forms and supplies.
Performs other duties that may be in accordance to documented procedures and reports results of assigned job to immediate superior.
Supports and actively participates in improvement projects as part of WCM program or Quality initiative.
Conducts Safety Behavioral Observation (SBO) and QBO and ensures engagement with concerned personnel are done in a timely manner
Bachelor’s degree – Chemistry, Chemical Engineering or any relevant course
Fresh graduates are welcome to apply
Flexible within pattern of shift work
Fast-learner and can easily adapt to the environment
Willing to be assigned in Paco, Manila
Job: Supply Chain
Primary Location: Philippines-Philippines (Region Level)-Manila-Paco
Shift: Day Job
Unposting Date: May-17-2018
Req ID: 1800062I