Assemble and/or repair product assemblies and components by following work orders, engineering drawings, standard operating procedures (SOPs), and verbal instructions.
Perform manufacturing processes such as bending, tacking, welding, tweaking, leak testing, and component assembly in accordance with approved specifications.
Operate production equipment, test fixtures, electronic measuring instruments, and leak detection equipment safely and effectively.
...
• Minimum SPM qualification or equivalent technical qualification.
• Previous experience in a cleanroom or manufacturing environment.
• Ability to read and interpret engineering drawings
blueprints
and work instructions.
• Attention to detail to identify product defects and maintain high-quality standards.
• Ability to stand and perform repetitive tasks for extended periods while working in a cleanroom environment.
• Comfortable in wearing full PPE - cleanroom garments
gloves
face mask
safety glasses
and other required PPE throughout the shift.
Lead and coordinate product registration, notifications, and variations with the National Pharmaceutical Regulatory Agency (NPRA / KKM).
Prepare, review, and organize complete regulatory dossiers, including dossier submission, Certificate of Free Sale, ingredients validation, etc.
Stay up to date with Malaysia food and health supplement regulations, ensuring all raw materials, formulations, and labeling meet current NPRA and KKM requirements.
...
Assemble and/or repair product assemblies and components by following work orders, engineering drawings, standard operating procedures (SOPs), and verbal instructions.
Perform manufacturing processes such as bending, tacking, welding, tweaking, leak testing, and component assembly in accordance with approved specifications.
Operate production equipment, test fixtures, electronic measuring instruments, and leak detection equipment safely and effectively.
...
• Minimum SPM qualification or equivalent technical qualification.
• Previous experience in a cleanroom or manufacturing environment.
• Ability to read and interpret engineering drawings
blueprints
and work instructions.
• Attention to detail to identify product defects and maintain high-quality standards.
• Ability to stand and perform repetitive tasks for extended periods while working in a cleanroom environment.
• Comfortable in wearing full PPE - cleanroom garments
gloves
face mask
safety glasses
and other required PPE throughout the shift.
Lead and coordinate product registration, notifications, and variations with the National Pharmaceutical Regulatory Agency (NPRA / KKM).
Prepare, review, and organize complete regulatory dossiers, including dossier submission, Certificate of Free Sale, ingredients validation, etc.
Stay up to date with Malaysia food and health supplement regulations, ensuring all raw materials, formulations, and labeling meet current NPRA and KKM requirements.
...
QA/QC Document Management: Maintain, log, and organize all QA/QC documentation, including Method Statements, Inspection and Test Plans (ITPs), Request for Inspections (RFIs), Non-Conformance Reports (NCRs), Corrective Action Reports (CARs), and Material Review Applications (MRAs).
EDMS & Register Maintenance: Operate and update the Electronic Document Management System (EDMS) and maintain accurate master document registers for all incoming/outgoing QA/QC transmittals.
Inspection & Testing Records: Coordinate the registration, distribution, filing, and close-out tracking of site inspection sheets, lab test reports (soil, concrete, asphalt, steel), and third-party test results.
...
Document Control
Quality Assurance
Quality Control
Construction Documentation
Project Management Software
Technical Documentation
Compliance
Auditing
Record Keeping
Information Management
QA/QC Document Management: Maintain, log, and organize all QA/QC documentation, including Method Statements, Inspection and Test Plans (ITPs), Request for Inspections (RFIs), Non-Conformance Reports (NCRs), Corrective Action Reports (CARs), and Material Review Applications (MRAs).
EDMS & Register Maintenance: Operate and update the Electronic Document Management System (EDMS) and maintain accurate master document registers for all incoming/outgoing QA/QC transmittals.
Inspection & Testing Records: Coordinate the registration, distribution, filing, and close-out tracking of site inspection sheets, lab test reports (soil, concrete, asphalt, steel), and third-party test results.
...
Lead and coordinate product registration, notifications, and variations with the National Pharmaceutical Regulatory Agency (NPRA / KKM).
Prepare, review, and organize complete regulatory dossiers, including dossier submission, Certificate of Free Sale, ingredients validation, etc.
Stay up to date with Malaysia food and health supplement regulations, ensuring all raw materials, formulations, and labeling meet current NPRA and KKM requirements.
...
QA/QC Document Management: Maintain, log, and organize all QA/QC documentation, including Method Statements, Inspection and Test Plans (ITPs), Request for Inspections (RFIs), Non-Conformance Reports (NCRs), Corrective Action Reports (CARs), and Material Review Applications (MRAs).
EDMS & Register Maintenance: Operate and update the Electronic Document Management System (EDMS) and maintain accurate master document registers for all incoming/outgoing QA/QC transmittals.
Inspection & Testing Records: Coordinate the registration, distribution, filing, and close-out tracking of site inspection sheets, lab test reports (soil, concrete, asphalt, steel), and third-party test results.
...
Maintain strong overall quality control for all products handled by the company.
Inspect incoming goods according to the required specifications, including general quality, product finishing, weight, dimensions, packing, packaging, product labels, barcodes, and other relevant requirements.
...
QA/QC Document Management: Maintain, log, and organize all QA/QC documentation, including Method Statements, Inspection and Test Plans (ITPs), Request for Inspections (RFIs), Non-Conformance Reports (NCRs), Corrective Action Reports (CARs), and Material Review Applications (MRAs).
EDMS & Register Maintenance: Operate and update the Electronic Document Management System (EDMS) and maintain accurate master document registers for all incoming/outgoing QA/QC transmittals.
Inspection & Testing Records: Coordinate the registration, distribution, filing, and close-out tracking of site inspection sheets, lab test reports (soil, concrete, asphalt, steel), and third-party test results.
...
Maintain strong overall quality control for all products handled by the company.
Inspect incoming goods according to the required specifications, including general quality, product finishing, weight, dimensions, packing, packaging, product labels, barcodes, and other relevant requirements.
...