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DXN International in Malaysia seeks an organized R&D Project Administrator to coordinate trials, manage documentation, and support procurement and data reporting. You will prepare protocols, batch records, and supplier communications, ensuring confidentiality and version control.
You will also coordinate material handling, assist in safety and compliance activities, and support management with routine updates. Fresh graduates may be considered for this role in a fast-paced R&D environment.
1. R&D Project Administration and CoordinationMaintain project trackers, schedules, trial plans and action lists. Arrange meetings, prepare minutes and follow up on outstanding actions with R&D, Production, QA/QC, Engineering, Procurement and suppliers.2. Technical Documentation and Records ControlPrepare, compile, format and maintain trial protocols, batch records, laboratory results, equipment specifications, quotations, comparison sheets, SOP/WI drafts, validation documents, reports and presentation materials. Ensure proper filing, version control, confidentiality and retrieval of records.3. Trial, Sample and Material CoordinationCoordinate the availability, identification, labelling, storage and movement of raw materials, ingredients, packaging materials, samples and trial outputs. Support the scheduling of laboratory testing, sensory evaluations, pilot trials and sample submissions, and maintain material and sample usage records.4. Procurement and Supplier Follow-upPrepare purchase requisition information and technical requirement summaries based on approved instructions. Request and compile supplier quotations, datasheets, certificates and delivery lead times. Follow up on deliveries, discrepancies and pending technical information, and expedite delays or issues to the Section Manager.5. Data Compilation and Reporting SupportCollect and organize trial and process data, including yield, extraction conditions, moisture, stability, viscosity, sensory results, softgel shell or product attributes, processing time and material consumption. Prepare tables, charts and preliminary summaries for the Section Manager’s review without independently approving technical conclusions.6. Compliance, Safety and Laboratory SupportFollow applicable GMP, HACCP, ISO 22000, laboratory safety, chemical handling, hygiene and document-control requirements. Assist in compiling supporting evidence for internal reviews, audits and regulatory or customer requests. Immediately report incidents, deviations, damaged equipment and unsafe conditions.7. Communication and Management SupportDraft routine emails, letters, meeting materials and progress updates for review and approval. Coordinate communication with suppliers and internal departments, prepare management summaries and support Chairman Office requests related to R&D projects while protecting confidential information.8. General Administration and Continuous ImprovementMaintain organized electronic and hard-copy project files, inventories and office records. Support improvements to administrative workflows, templates, dashboards and reporting systems. Perform other R&D coordination duties assigned by the Section Manager or an authorized superior.