Support QA/QC documentation activities, including document control, filing, record maintenance, and database updates in accordance with company procedures and regulatory requirements.
Participate in quality system administration and continuous improvement initiatives.
Provide general administrative support to the Regulatory Affairs and QA/QC teams and assist with other assigned tasks as required.
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Work closely with engineers and product owners locally
Log, track and document bugs discovered during testing as well as gather all necessary information. Perform regression, installation, and upgrade testing in every release cycle
Experience in Salesforce technology (Optional)
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Hands on experience in QA/QC operation in a manufacturing environment with ISO 9001:2015
Experience in SOP creations, Well-wisher & fast, accurate solution finder for Customer Complaints and regulatory affair matters related to printing and plastic packaging product is an added advantages to apply.
Assist General Manager to oversee the entire QA/QC operation and ensure smooth operation of the department
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Lab maintenance; maintain a clean and organized laboratory workspace, ensure safe handling and disposal of chemicals and hazardous materials, adhere to safety protocols, accurate ordering of lab materials and equipment, maintain stock record of retained production and lab samples, raw materials, additives, and fragrances
Monitor production activities; process and procedures followed according to SOP, develop and implement QC procedures to ensure consistency and compliance to specification standards, issue and review analysis documents such as COA and MSDS, issue and maintain accurate working files such as BOM, purchase requisition, production instruction, and batch manufacturing record online (ERP system) and offline, carry out CAPA activity on NC product, participate in training and audit activities
Timely coordination with internal teams on product development, result documentation, and other information and tasks as per required
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Assist in Statistical process control and process capability assessment in the validation program.
Undertake margin expansion, PPV and CIP’s opportunities for site and corporate where necessary in the are of material or packaging substitutions initiatives and cost reduction where applicable.
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Participate in strategic planning and in the formation of department policies, procedures, organizational structure, and direction.
Identify, track and respond to metrics relevant to the department's performance.
Interact with senior management and engineering personnel to help establish priorities, allocate personnel, define project objectives and determine target completion dates.
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Assist in Statistical process control and process capability assessment in the validation program.
Undertake margin expansion, PPV and CIP’s opportunities for site and corporate where necessary in the are of material or packaging substitutions initiatives and cost reduction where applicable.
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