Manufacturing quality assurance

873538

CRC ¢ 2 a 2 ,5 millones

Costa Rica Alajuela

Publicado 26 Ene 2026

Producción: planta

1 Vacante

Ingeniería Industrial / Otras

Confidencial
Industria de la empresa:
Servicios

Descripción general

Responsible for leading and managing all MEVS QA activities at the manufacturing site to ensure compliance with applicable regulatory requirements (including but not limited to 21 CFR 820, ISO 13485, ISO 13408, EU MDR, MDSAP), company policies and industry standards. This role is critical in maintaining product quality, patient safety, continuous improvement and regulatory compliance for the MEVS.

Experience:
• Minimum 10 years of experience in Quality Assurance within the medical device industry.
• Minimum of 7 years of supervisory experience.
• Proven leadership experience managing QA teams and site-level quality operations.
• In-depth knowledge of 21 CFR 820, ISO 13485, EU MDR, MDSAP, and other global standards.
• In-depth knowledge of ISO 13408, aseptic processing, and contamination control strategies.


Education:
• Bachelor’s degree in engineering (Mechanical, Biomedical, Industrial, or related field), health, or life science field; master’s degree preferred.

Competencias para la vacante

Datos complementarios

873538

Profesional

Bachillerato universitario

Industria farmacéutica

7 años de experiencia

873538

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