Execute assigned manufacturing tasks and activities according to production schedule incompliance with the relevant GMP, safety and environmental guidelines.
Perform routine operational support activities according to the manufacturing process and schedule and enable the timely production of product with the quality and quantity.
Major Accountabilities
Domain specific main activities
Participation to the manufacturing support processes
Execution of all assigned activities according to production schedule and in compliance with the valid GMP, work, operating, environmental and safety instructions and guidelines.
Batch record review on time and without error (production part)
Proper and timely cleaning, preparation and sterilization of the production equipment andproduction rooms
Equipment parts management (punch, sieve etc.)
Support on cleaning and changeover
Work permit coordination where applicable
Material movement in shop floor (including dispensing)
Waste material management and pre-treatment of liquid waste streams) at shop floor
Raw material ordering (filling daily tanks of solvents, Kanbans, packaging materials)
Responsible for production area housekeeping (cleaning, tidiness, 5S...)
Comply with and enforce health, safety and environment rules and guidelines (HSE)
Apply and enforce the current GMP rules
Sampling, aliquoting, distribution and performing of in-process controls
Implementation of the delegated environmental monitoring for clean rooms and the delegated sampling of ultrapure water and pure steam if applicable
Organization of immediate measures in the event of a fault, reporting abnormalities to the manager; experts and operational QA
Ensure / monitor the proper functioning of the equipment in order to detect early signs of anomalies. Take appropriate action in the event of a malfunction.
Documentation of the activities according to GMP regulations
Manage the consumables supply necessary for the proper functioning of operations
Sort and eliminate waste related to production activities
Daily checks of manufacturing equipment, support devices and rooms
Clearly and precisely document the necessary remarks in the batch records
Participate in the production schedule building-up (report delays, wrong activities duration...)and comply with it
Commitment and participation to operational excellence and continuous improvement
Proper handling of biological and chemical substances in the production plant
Participation in all training relevant to the position, maintenance of the relevant training evidence
Advancing and maintaining an HSE-compliant environment: reporting near misses
Non domain specific main activities
Perform manufacturing related ERP transactions/activities
Perform IPC related activities in LIMS or ERP system
Participate in investigations in the context of deviations, OOS, OOE, etc.
HSE and Quality
Promote and improve the Safety and Quality cultures
Apply in practical the upgrading, and the improvement of Safety and Quality on the shop floor
Ensure overall inspection readiness for area of responsibility
Supervision in their area, incident reporting and action follow-up at shop floor level
Ensure the availability and proper use of Protective Equipment
Comply with safety, cleanliness and tidiness rules (housekeeping, 5S)
Detect and report potential accident, risks and propose solutions
Preparation and participation to internal HSE audits
Operational Excellence and continuous improvement
Willingness to continuously improve and analyze weak points
We are a process automation service provider for the life science industry. We provide automation solutions and manpower resources for day-to-day operations and projects.
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