Nikita Drummond

• Ensure that all Quality Assurance documents, and production records are available with each production run.
• Ensure that all production data has been accurately entered into our inventory system for each production run.
• Monitor MD /Kanban of our 80 parts and to ensure adherence to our visual management.

• Responsible for various QA functions, including but not limited to the adherence of our Quality Management system and maintaining raw material and component traceability.

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Coordinate and schedule all document control review and audits with the Quality Technician utilizing the Quality Management system.

Support the Quality Technician in the creation of standardized forms, work instructions, SOPs, Ps, and policies.

Ensure all documentation aligns directly with the Internal Quality Assurance Manual and ISO 9001.

Assist in Corrective/Preventative Action, Non-Conformance, and Return Material Authorization procedures.

Assist Quality Technician with all on-going various compliance-related documentation.

Provide technical assistance to production and quality staff on QA/QC issues.

Assist Quality Technician and Production Manager with preparing reports through collecting, analyzing, and summarizing data; make recommendations for corrections and/or improvements.

• Complete reviews of Product Technical Files with Product Design Engineer to ensure required testing data, and that documentation is in place and readily accessible.
• Ensure that adequate materials and consumables are available to achieve the production plan using a Kanban system.
• This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary.ws

• Refer to the appropriate Standard Operating Procedures.
• Each shift hand over discuss any production issues with the other machine operators.
• Report any quality, safety or other concerns to your Supervisor and other appropriate staff.
• Ensure the work areas around the injection moulding machines are kept tidy and organised.
• Read the works order production planning card requirements.
• Start-ups, ensure all paper work is organised and completed for start-up approval, including a start sample, QC gauges and labels.
• Check and record part inspections in accordance to the QC Inspection Plan & Record,
  QG Inspection Drawing and related paper work.
• Regularly check machines to ensure there are no obvious mould or machine issues.
• Ensure production boxes at the machines are not overfilling and replaced as required.
• Final weigh count, inspection and labelling of each box before stacking on the pallet.
• With your Supervisor, ensure production identified not suitable for use, which does not meet specification, or in your judgement is not suitable for the intended application is isolated and clearly labelled and put in the hold area.
• Wastage must be recorded on the Works Order Material Wastage Record.
• End of run, ensure all paper work is collected and put into the completed works order holder on the machine. QC Gauge, start sample is filed in the QC Office with end of run sample which must be taken before the machine is stopped.

• Cleaned and stocked guest rooms by replacing used towels and linens, making beds, and restocking bathroom items.
• Replenished amenities(teas/coffee/milk etc)
• Washed and put away kitchen dishes, utensils and glassware.
• Spray, clean and disinfect bathroom(basins, shower, toilet, mirror etc)
• Swept high ceilings, tight spaces and around furniture to remove built up dust and cobwebs.
• Dusted and wiped down furniture, fixtures, and window sills to keep areas clean and comfortable.
• Emptied the trash
• Vacuumed and mopped floors
• Disinfected and mopped public restrooms around the hotel to keep facilities sanitary and clean.
• Restock trolley with fresh linen, towelling and amenities for the next day.

Mentioned above.