Job Description

Roles & Responsibilities

• Evaluate and maintain product and service quality.
• Resolve equipment and process-related production issues.
• Conduct equipment, process, materials, and method validation.
• Perform statistical analysis and metrics to assess systems and processes.
• Develop and execute test protocols, collect data, and write validation reports.
• Collaborate cross-functionally in product/service development or maintenance.

Experience Required

• Minimum 2 years of applicable experience in a related role.
• Experience with GMP in medical devices and/or pharmaceuticals is a must.
• Supplier quality experience is a plus.

Skills & Certifications

• Basic knowledge of quality engineering policies, principles, and best practices.
• Basic statistical sampling and analysis skills.
• Competence in writing test protocols and validation reports.
• Strong problem-solving and analytical abilities.

Eligibilities & qualifications

• Bachelor’s degree (BS) or equivalent required.
• Basic knowledge of theories, practices, and procedures in quality engineering.
• Ability to work under direct supervision and perform routine tasks.

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