Manufacturing Science and Technology Engineer

Confidential Jobs; Naucalpan de Juárez; On-site; MXN 600,000 - 1,000,000; Full time

Job summary

A leading company in medical devices is seeking a Manufacturing Science and Technology Engineer to investigate quality-related issues, collaborate with multiple teams, and ensure compliance with regulatory standards. The ideal candidate has a Master’s degree, excellent analytical skills, and 5+ years of experience in a regulated industry. This full-time role is based in Naucalpan de Juárez, Mexico.

Qualifications

• Minimum of 5 years of experience in a medical devices or regulated industry.
• Ability to influence in a matrix organization.
• Willing to travel at customer, suppliers or other sites upon request.
• Excellent analytical and problem-solving skills.
• Proficiency in technical writing and documentation.
• Ability to work self-directed at a fast pace with multiple tasks.
• Ability to influence in a matrix organization.
• Statistical knowledge.

Responsibilities

• Collaborate with various teams to complete Root Cause Analysis and CAPAs.

Skills

Professional English (written and oral)

Excellent analytical and problem-solving skills

Proficiency in technical writing and documentation

Teamwork skills

Statistical knowledge

Self-directed work

Matrix organization

Education

Master of Science in Quality Assurance or Engineering

MS in Engineering or science discipline

Job description

Manufacturing Science and Technology Engineer

The Manufacturing Science and Technology Engineer is responsible for conducting thorough investigations of customer complaints, internal non-conformances, and other quality-related issues within a Medical Devices environment. The role ensures compliance with regulatory standards and internal procedures, aiming to identify root causes and implement corrective and preventive actions (CAPA).

Responsibilities

• Collaborate with Manufacturing, Engineering, Supply Chain, Quality Platform, R&D, Design Assurance, Technical Services, Customer and Suppliers to ensure completion of Root Cause Analysis, CAPAs and Effectiveness Checks.

Qualifications

• Position requires a sound Quality or technical/Engineering background. Master of Science in Quality Assurance or Master of Science in Engineering or science discipline.
• Professional English (written and oral)
• Minimum of 5 years of experience in a medical devices or regulated industry.
• Excellent analytical and problem-solving skills.
• Proficiency in technical writing and documentation
• Ability to work self-directed at a fast pace dealing with multiple tasks.
• Ability to influence in a matrix organization
• Analytical - Synthesizes complex or diverse information.
• High positive energy to take on continuous and complex business challenges in a fast-paced environment.
• Persistence to drive to solutions despite obstacles and/or competing priorities.
• Teamwork skills: Ability to work with diverse teams across the organization.
• Judgment and decision-making skills supported by sound technical & business justification.
• Demonstrated ability to discuss both technical and business issues with all levels of management, Customers and Suppliers.
• Statistical knowledge
• Willing to travel at customer, suppliers or other sites upon request.

Seniority level

• Executive

Employment type

• Full-time

Job function

• Manufacturing

Industries

• Pharmaceutical Manufacturing