Product Introduction Engineer

ICU Medical; Ensenada; Presencial; MXN 300 000 - 420 000; Tempo integral

Resumo da oferta

ICU Medical in Ensenada seeks a qualified professional with a B.S. in Industrial Engineering or related field to support manufacturing processes. The candidate should demonstrate strong communication and organizational skills, and proficient use of Minitab and Microsoft Office.

Fluency in English (90%) is required to communicate effectively with international teams. The role requires knowledge of Lean Manufacturing, JIT, Kaizen, TPS, and Six Sigma production systems, along with GMP familiarity

Qualificações

• Bachelor’s degree in Industrial Engineering or related field.
• Strong communication and organizational skills.
• Proficiency in computer software packages including Minitab, Microsoft Office, etc.
• 90% English proficiency (spoken and written).
• Knowledge of Lean Manufacturing, JIT, Kaizen, TPS, and Six Sigma production systems.
• Knowledge and/or use of Quality tools and sampling plans.
• Validation process skills.

Responsabilidades

• One 1–3 years of experience in manufacturing processes, preferably medical devices.
• Required knowledge of Good Manufacturing Practices (GMP) and regulations applicable to the medical industry.
• Personnel supervision skills are desirable.
• Compliance with GMP regulations and all national and international quality standards in accordance with the Quality Manual

Conhecimentos

Strong communication

Organizational skills

90% English proficiency

Lean Manufacturing

JIT

Kaizen

TPS

Six Sigma

Quality tools

Sampling plans

Validation

Formação académica

Bachelor’s degree in Industrial Engineering or related field

Ferramentas

Minitab

Microsoft Office

Descrição da oferta de emprego

• Bachelor’s degree in Industrial Engineering or related field.
• Strong communication and organizational skills.
• Proficiency in computer software packages including Minitab, Microsoft Office, etc.
• 90% English proficiency (spoken and written).
• Knowledge of Lean Manufacturing, JIT, Kaizen, TPS, and Six Sigma production systems.
• Knowledge and/or use of Quality tools and sampling plans.
• Validation process skills.

• One 1–3 years of experience in manufacturing processes, preferably medical devices.
• Required knowledge of Good Manufacturing Practices (GMP) and regulations applicable to the medical industry.
• Personnel supervision skills are desirable.
• Compliance with GMP regulations and all national and international quality standards in accordance with the Quality Manual