• Guides the potential uses of healthcare technology and outlines the opportunities and limitations of the technology/services• Ensure regulatory compliance by reviewing technical files and design dossiers, confirming adherence to regulatory requirements• Review and enhance technical specifications, ensuring comprehensive documentation for MOF and MOH tender bidding submissions• Conduct thorough market research to identify trends, competitor activities, and opportunities, applying the findings to implement effective marketing strategies• Collaborate with cross-functional teams to develop and execute strategic marketing support, creating sales collateral, technical presentations, and promotional materials• Foster effective communication between healthcare professionals and stakeholders, addressing queries, and proactively resolving issues, to promote a collaborative environment• Accountable for assessing and researching medical devices, conducting cost-benefit analyses, and evaluating clinical efficiency and outcomes• Consistently meet ad-hoc project milestones and deadlines, successfully executing sales revenue• Stay informed on the latest advancements in medical research, regulations, and healthcare industry issues to ensure project compliance and adherence to industry standards• Support additional tasks assigned by superiors, demonstrating flexibility and a commitment to team success within a multidisciplinary healthcare team

• Responsible for regulatory compliance of medical devices, licenses, and intellectual property• Prepared documents for submission of medical device registration, and ensured timely renewal of product registrations and licenses• Maintained regulatory files and documentation for ISO 13485, and was responsible for internal and external audits such as BSI ISO 13485 audits, GDPMD audits, and financial audits• Reviewed company’s practices in compliance with regulatory requirements, and advised on regulatory requirements, legal and scientific restraints• Maintained familiarity with current industry practices that affect regulatory affairs function• Reviewed and approved the technical content of the material to ensure compliance with legal requirements

Technical Duties:• Validated and verified all tests conducted with valid internal quality control• Validated and verified all results from machines before release results into LIS• Coordinated with the IT team on the implementation and optimization of LIS, and to provided feedback on the system interfacing, enhancement or fix issues• Assisted manager in oversee the whole lab operations and to notify critical test results• Provided technical training’s on lab workflow to new staffs• Ensured a smooth running of operation and staff matters (e.g. morale, optimum work allocation, interdepartmental relationship, schedule planning, leave coverage)Administrative Duties:• Data transcription, results interfacing, and released of results (final verification of test reports) into BP Lab Information System (BP LIS), within the given turn-around-time; 24Hrs TAT• Attended to all emails and WhatsApp tracing daily, and alert the lab team about the urgency of samples• Registration and bulk registration of clinic and hospital KKM samples into the system accordingly, and ensured that the sample amount received are tallied with request forms• Answered any inquiries from doctors, to conduct investigations on customer complaints, and to conduct corrective actions and preventive actions of any non-conformance• Maintained confidentiality of patients information gained in the conduct of testing, and not disclose the results or information to unauthorized persons, without the consent of the person concernGeneral Duties:• Multitasked and lended a helping hand in different workstation simultaneously when sample surge or load is high, to ensure the TAT is achieved• In-charged on stock count inventory, ensured the stocks are adequately maintained, and liaised with the purchasing department for the arrival of new stock of consumables and reagents• Assisted on the documentation preparation for ISO lab audit and ensured all documentations are maintained in proper

1) Conducted qualitative screening of viral nucleic acid for Novel Coronavirus 2019-nCoV of the following work:• Reviewed the sample condition upon receival, and ensured that the sample amount received are tallied with log sheets or request forms• Sorted the samples by prioritizing to its urgency, incubated the swab samples, and registered the samples into the database accordingly, before proceeding for nucleic acid extraction (RNA extraction)• Prepared RNA extraction buffers followed by sample loading into 96-well plate for RNA extraction• Prepared RT-PCR mastermix and transferred extracted RNA samples; either in 96-well plate reaction (manual run) or 384-well plate reaction (operation of automated liquid handling platform)• RT-PCR curve and CT value analysis in thermocycler by interpreting the fluorescence signals• Administration work, result interfacing, report validation and final verification, and result tracing• Verified results reported to the requestor within the given turn-around-time (within 24Hrs TAT)• Maintain a responsible approach concerning the handling and disposal of hazardous material2) Conducted DNA and RNA viral load of hepatitis virus (Hepatitis B and Hepatitis C) serum samples, and human papillomavirus cytology samples via Roche Hamilton Cobas 4800 System

• Performed ELISA screening for Hepatitis B, Hepatitis C and IgG• Conducted immunology screening of blood serum samples via Abbott Alinity CI• Data entry validation

• Recruited and enrolled qualified students to the University, accelerating average monthly sales of 80%• Analyzed marketing strategies and implemented marketing directions to the team• Provided consultation and guidance on enrolment requirements and related issues• Provided information on the courses offered to prospective and existing students• Maintained consistent contact with students throughout the enrolment process• Assisted in preparation of marketing events (e.g. roadshows, interviews and career fair), budget and sales report, and administrative duties

• Schottky diode fabrication• Acquisition of Current-Voltage (I-V) curve of biological samples (nucleic acids and whole-cells) in LabVIEW• Data analysis and calculation of solid-state parameters• Optimization of I-V results with biological and technical replicates of samples• Supervised undergraduates working on the research project and monitored their progress• Prepared proposal writing for grant submissions and patent filing, and monitored the project budget

• Gene expression studies of shrimps viruses in aquaculture farms• Supervised undergraduates working on the research project and monitored their progress• Prepared proposal writing for grant submissions and patent filing, and monitored the project budget• Procured laboratory equipment supplies and recorded inventory counts for audit inspections

• Isolation and species identification of toxic algae and cyanobacteria• DNA amplification of microcystin gene (toxin gene) in cyanobacteria• Gene expression studies of algae and cyanobacteria

• Research project on the anatomy structure and archaeology studies of catfish species• Assisted supervisor in administration duties and journal publications

• Generated an average weekly sales of RM3000• Conducted training and development modules on team building• Provided marketing directions and boosted confidence to the team members• Responsible in recording inventory counts during stock arrival