C
Cardinal Health 222 (Thailand) Ltd.
Engineer II (Material Science)
Skills
RCompliance
1 month ago
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Important information
Contract type:
Permanent
Location:
Rayong, Mueang Rayong District, Rayong, Thailand
Work mode:
Onsite
Published on:
25 September 2026
What they need
Location: Rayong, Thailand
Reporting to: Manufacturing Engineering Assistant Manager
Summary
- Lead material characterization activities to establish material specifications and testing requirements following CTQ principles.
- Provide technical expertise in material improvement, validation, and technology scale-up, including new material development and alternate source qualification.
- Collaborate with R&D and Packaging Technology teams to ensure full understanding of material characteristics, usage impact, and testing requirements.
Job Description
- Lead new material development projects and alternate material/source qualification to support business continuity and cost improvement.
- Conduct laboratory trials for new or alternative materials and provide study results to support feasibility studies and validation protocols.
- Collaborate with universities, research institutes, and external partners to advance material technologies and establish material specifications and test requirements.
- Coordinate with Packaging Technology to understand new packaging technologies related to materials and machinery.
- Work closely with R&D, Packaging Technology, and Purchasing to define material specifications and testing requirements for new materials.
- Provide technical support for material-related issues and participate in MRB evaluations when required.
- Monitor key material property trends, conduct correlation studies with product quality, and recommend appropriate actions.
- Support VIP projects and other strategic initiatives related to material science.
- Support additional tasks related to the role as needed.
- Ensure compliance with company GMP, safety, and EHS standards.
Qualifications & Experience
- Bachelor’s degree in Chemical Engineering, Polymer Science, Chemistry, or a related field.
- Minimum 3 years of manufacturing engineering experience; experience in glove manufacturing is advantageous.
- Strong technical competence in material development, validation, and process optimization.
- Experience in process development, optimization, DOE, correlation studies, and experimental design.
- Proficiency in statistical analysis tools such as Minitab, JMP, SPSS or similar statistical software.
- Knowledge of FDA medical device validation requirements is preferred.
- Strong leadership and problem-solving skills with the ability to work effectively across cross functional teams.
- Excellent teamwork, coordination, and interpersonal skills.
- Native Thai and advance English skills (written, verbal and presentation skills).
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