Work closely with the Engineering team to ensure process changes are incorporated into
Trains manufacturing operators on a variety of manufacturing processes at workstations and in the classroom, including, but not limited to processes, equipment operation (setup, operation, cleaning, troubleshooting), documentation handling, material handling, etc.
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Work closely with the Engineering team to ensure process changes are incorporated into
Trains manufacturing operators on a variety of manufacturing processes at workstations and in the classroom, including, but not limited to processes, equipment operation (setup, operation, cleaning, troubleshooting), documentation handling, material handling, etc.
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Ensure microbiology laboratory equipment and facilities are maintained in a qualified, calibrated, safe, and fit-for-purpose condition, and coordinate required maintenance, calibration, qualification, and corrective actions.
Lead and support the development, validation, verification, transfer, and implementation of microbiological test methods, including evaluation of method suitability and robustness, to support laboratory capability and business needs.
Monitor execution of routine product bioburden and/or bacterial endotoxin testing. Ensure testing is performed in accordance with approved procedures, applicable standards, and established laboratory requirements.
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Ensure microbiology laboratory equipment and facilities are maintained in a qualified, calibrated, safe, and fit-for-purpose condition, and coordinate required maintenance, calibration, qualification, and corrective actions.
Lead and support the development, validation, verification, transfer, and implementation of microbiological test methods, including evaluation of method suitability and robustness, to support laboratory capability and business needs.
Monitor execution of routine product bioburden and/or bacterial endotoxin testing. Ensure testing is performed in accordance with approved procedures, applicable standards, and established laboratory requirements.
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Monitor process performance through data analysis and quality metrics, identifying opportunities for continuous improvement and operational excellence.
Contribute to internal and external audit activities, while promoting quality awareness and best practices across the manufacturing operation.
Degree in Engineering, Science, Manufacturing, Quality, or a related discipline.
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Use appropriate quality tools and statistical techniques to collect and summarize data, draw conclusions with confidence, determine sample sizes, apply data distributions, identify relationships between variables, calculate reliability, design and analyze experiments, determine process and
Apply the most relevant and useful quality philosophies throughout Design Control and its related processes for both new product development and sustaining. Understand and manage work to minimize cost of quality throughout the product’s lifecycle.
Ensure compliance of all practices to the Quality Management System. Ensure comprehensive documentation is available, adequate records are produced, and change management is implemented.
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Coordinates cross-functionally with marketing, clinical, sales, regulatory, operations (Internal/External) and shared services teams to define and document user needs, design inputs and outputs, design transfer and commercialization deliverables as per the design control procedure.
Document all new ideas for products and/or processes which should be assessed for intellectual property opportunity. Work with the legal team to file new patents and assess potential for infringement
Coordinates the development of concepts, prototypes, and corresponding test methods for rapid development cycles.
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Communicate with Regional RA to ensure timely notification of changes as appropriate. Partner with Regional RA to support registration of product in foreign markets. Fulfill basic requests and coordinate with applicable RA staff regarding more complex requests.
Support regulatory compliance activities, including Health Canada license renewals, Food and Drug Administration (FDA) product device listings, establishment registrations, inspections, audits, etc under supervision
Review and provide feedback to risk management assessments and design control deliverables, as necessary to ensure that it follows the regulatory requirements under supervision.
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To do and ensure the cleanliness of lorry every day under store and warehouse responsibility.
To check, maintain and update superior all the equipment under store and warehouse responsibility on daily basis in good condition and safe to use from time to time.
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Responsible report to Seamer Supervisor or Senior Seamer Technician if found any of double seam which out of acceptable range or critical limit during seaming process.
To check and ensure the safety devices for the seamer machine are in workable condition
To liaise with quality team if found any problem occurs during production which related to quality issue.
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