Deskripsi Pekerjaan
Are you a seasoned Injection Molding professional with a passion for bringing new products to life? Mehow Medical (M) Sdn Bhd is seeking a highly skilled Injection Molding Process Engineer to lead our New Product Introduction (NPI) initiatives. In this pivotal role, you will be the bridge between design and mass production, ensuring our high-precision medical components meet the most stringent quality standards.
You will play a central role in driving manufacturing excellence by managing complex mold trials, overseeing comprehensive process validations (IQ/OQ/PQ), and mitigating production risks early in the development lifecycle. If you thrive in a fast-paced environment and possess a deep technical understanding of plastic resins, mold flow analysis, and automated assembly, we invite you to join our world-class engineering team in Simpang Ampat.
Tanggung Jawab
- Lead NPI projects from the design stage through to successful mass production hand-over.
- Coordinate and execute mold trials, troubleshooting technical issues to optimize cycle times and part quality.
- Perform comprehensive process validation (IQ/OQ/PQ) in accordance with medical industry standards (ISO 13485).
- Conduct detailed risk assessments, including PFMEA, to proactively identify and mitigate manufacturing challenges.
- Collaborate with cross-functional teams, including Tooling, Quality, and Production, to resolve technical bottlenecks.
- Utilize scientific molding principles to establish robust and repeatable injection molding processes.
- Support the selection and qualification of new molding equipment and peripheral automation systems.
Kualifikasi
- Bachelor’s Degree in Mechanical, Manufacturing, or Polymer Engineering.
- Minimum 3-5 years of hands-on experience in plastic injection molding, specifically within the medical device or high-precision industry.
- Proficiency in Scientific Molding principles and process optimization techniques.
- Strong knowledge of mold design, runner systems, and various thermoplastic materials.
- Hands-on experience with DOE (Design of Experiments) and root cause analysis tools (8D, fishbone).
- Excellent communication skills with the ability to lead technical discussions and projects.
- Familiarity with ISO 13485 and cGMP requirements is highly preferred.