Participate in the opportunity review meetings to provide professional feedbacks regarding the tooling / fixture / mold required for the new product manufacturing and the related cost.
Prepare the part and the assembly drawings for the tooling / fixture; identify the proper vendor; and follow up with the schedule and cost to make sure they are made on time and within budget.
Perform tooling / fixture testing before the production use, write the work instruction if needed and train the production employees.
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Industrial Insights: Be part of a team with diversed engineering specializations. Work alongside with professionals from different field of expertise and gain valuable insights to Process Engineering, Commissioning and Validation, Instrumentations and Automation, Mechanical Engineering, Facility Management
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You will support to develop specifications, standards & review improvement, and investment proposals to upgrade and expand facilities.
You will also support early-phase design and feasibility studies, review site standards and propose design adaptations to overcome various engineering constraints.
Demonstrate creative mindset in problem solving and performance improvement including research and data analysis to support project decision-making.
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Exposure to manufacturing or operations-related activities through academic projects, coursework, internships, or part-time work will be an added advantage. The role is based in Batu Kawan, Penang, and offers an opportunity to build practical experience within a structured manufacturing environment.
The candidate is expected to possess strong technical and interpersonal competencies, including proficiency in Microsoft Office applications (particularly Excel and PowerPoint), effective communication, and the ability to work both independently and collaboratively. In addition, they should demonstrate initiative, problem-solving skills, good time management, and the ability to organize and synthesize information into actionable insights while managing multiple tasks in a dynamic environment.
Proficiency in Microsoft Word, Excel, and PowerPoint includes a range of skills from basic document creation to advanced data analysis and presentation design
Accurately input and maintain routing data in SAP, including machine line speed, setup time, and routing codes, ensuring all entries are updated in accordance with approved production parameters.
Assign appropriate machines to specific cable designs and processes in SAP, and maintain machine capability mapping to ensure correct linkage between product design, process routing, and machine availability.
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The role is based in Batu Kawan, Penang and requires a Bachelor’s degree in Microbiology, Biotechnology, Biological Sciences, or a related field. Candidates with certifications such as ISO 13485 Internal Auditor, sterilization standards (ISO 11135/11137), cleanroom monitoring, GMP, or root cause analysis have an added advantage. The position typically requires 3–5 years of relevant experience in microbiology, contamination control, or quality engineering within a regulated environment, with hands-on exposure to environmental monitoring, cleanroom operations, microbiological testing, and validation activities. Strong knowledge of ISO standards, along with technical writing and data analysis skills, is essential.
From a competency perspective, the role demands strong technical microbiology expertise combined with problem-solving and analytical skills. The candidate should be detail-oriented, capable of working independently, and able to communicate effectively while collaborating across functions such as Quality, Manufacturing, and Engineering. A strong commitment to quality, compliance, and regulatory requirements is critical, along with the ability to manage documentation accurately and consistently.
The role involves working in cleanroom and controlled environments, requiring adherence to strict gowning and contamination control standards. It may include physical tasks such as accessing elevated areas for sampling, handling equipment, and supporting environmental monitoring activities. Occasional travel (less than 10%) to external sterilization sites is required, and the candidate must be flexible to work outside standard hours, including evenings or weekends, to support validation activities and project milestones.
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