Strategic Supplier Quality Engineer II

Diasorin; Cypress (CA); Presencial; USD 69.000 - 117.000; Jornada completa

Descripción de la vacante

Diasorin is seeking a Diagnostics Specialist in the United States to oversee supplier quality and manufacturing interfaces. You will collaborate across Engineering, Sourcing, Quality Assurance, and Production to drive supplier performance and process improvements.

The role requires strong quality engineering experience, FDA/cGMP knowledge, and leadership in supplier audits and changes. Excellent communication and project management are essential.

Formación

• Bachelor's degree in a technical field.
• 7+ years related experience and/or training.
• 4+ years quality, supplier quality, or manufacturing experience.

Responsabilidades

• Monitor and measure supplier performance through production line statistics and audits.
• Establish and report supplier quality metrics as required.
• Utilize quality engineering principles to develop supplier performance.
• Assist in supplier selection & qualification for new products and sourcing.
• Participate in supplier conferences, site visits and audits.
• Lead corrective actions for low-performing suppliers.
• Lead or assist in specification development for materials and products.
• Participate in product planning and material review processes.
• Drive continuous improvement projects with suppliers.
• Lead or assist in supplier audits and audit reporting.

Conocimientos

Communication skills

Statistical analysis

Problem solving

Time management

Independent work

Deadline management

Microsoft Office

Educación

Bachelor's degree in a technical field

7+ years related experience

4+ years quality/supplier/manufacturing experience

Herramientas

CMM experience

Descripción del empleo

Diasorin is seeking a Diagnostics Specialist in the United States to oversee supplier quality and manufacturing interfaces. You will collaborate across Engineering, Sourcing, Quality Assurance, and Production to drive supplier performance and process improvements.

The role requires strong quality engineering experience, FDA/cGMP knowledge, and leadership in supplier audits and changes. Excellent communication and project management are essential.