Deskripsi Pekerjaan
Are you a driven engineer ready to make a tangible impact on global healthcare solutions? Cardinal Health is seeking a dynamic Manufacturing Engineer to join our team in the Central Region. In this high-visibility role, you will be the cornerstone of our APAC manufacturing success, serving as a vital partner to our production facilities and solving complex engineering challenges that directly influence product quality and operational excellence.
As a Manufacturing Engineer at Cardinal Health, you will lead cross-functional teams through the entire lifecycle of product launches, ensuring that our innovative medical products meet the highest standards of safety and efficiency. This position offers a unique opportunity to bridge the gap between technical design and large-scale manufacturing, providing you with a platform to influence regional strategy and drive process improvements across our supply chain.
Tanggung Jawab
- Lead end-to-end manufacturing process implementation for new product launches across the APAC region.
- Collaborate with cross-functional teams, including R&D, Quality, and Supply Chain, to resolve technical bottlenecks and optimize production workflows.
- Conduct root cause analysis for manufacturing deviations and implement robust corrective and preventive actions (CAPA).
- Drive continuous improvement initiatives to enhance production efficiency, yield, and cost-effectiveness.
- Standardize manufacturing documentation, including SOPs, work instructions, and validation protocols.
- Provide technical leadership and mentorship to junior engineering staff and production operators.
- Manage relationships with regional manufacturing partners to ensure compliance with strict regulatory and quality standards.
Kualifikasi
- Bachelor’s degree in Mechanical, Industrial, Chemical, or Biomedical Engineering.
- Minimum of 3-5 years of experience in a manufacturing engineering role, preferably within the medical device or pharmaceutical industry.
- Demonstrated expertise in Lean Manufacturing, Six Sigma, and process optimization methodologies.
- Strong technical background in equipment validation (IQ/OQ/PQ) and GMP environments.
- Proven ability to manage cross-functional projects and lead teams through complex product launches.
- Excellent analytical, problem-solving, and communication skills in a fast-paced environment.
- Proficiency in CAD software and data analysis tools (e.g., Minitab, Excel, or ERP systems).