Engineer Specialist- Manufacturing Improvement

Zvh; Tijuana; On-site; MXN 600,000 - 800,000; Full time

Job summary

Baxter in Mexico is seeking a Mechanical Manufacturing professional to help integrate and improve device manufacturing processes. You will lead significant projects, manage timelines and budgets, and drive cost quality improvements across operations.

The role requires five years of related experience in ISO/FDA-regulated environments, strong problem-solving and project-management skills, and advanced English abilities. This position is based in Tijuana.

Qualifications

• Bachelor's degree in an engineering field is required.
• Minimum of five years of related experience.
• Experience in ISO/FDA-regulated environments and GMP requirements.
• Experience writing and executing process validations (IQ/SV/DOE/OQ/PQ).
• Advanced English communication skills.

Responsibilities

• Lead Margin Improvement Projects (MIP) per the plant plan and departmental commitments.
• Ensure timely implementation of projects without impacting manufacturing lines.
• Identify opportunities for MIP projects through ideas related to direct materials and validate savings.
• Collaborate with Procurement for quotations and feasibility assessments.
• Lead Workshops, Kaizen, and VAVE events for MIP ideas with cross-functional teams.
• Lead project planning including scheduling, costs, and resources.
• Develop and complete process validation activities (IQ/SV/OQ/PQ/TMV) per SOPs and GMP.

Skills

Lean practices

Six Sigma

Project management

Leadership

Problem solving

Cross-functional collaboration

Education

Bachelor's degree in Mechanical / Mechatronics / Electrical / Electromechanical / Systems Engineering or related field

Tools

IQ/SV/OQ/PQ

Job description

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

Responsible for the integration of existing processes (through transfers from other Baxter sites) and the development and continuous improvement of mechanical device manufacturing processes. May have full project ownership for significant projects within the specialized area. Responsible for the development and improvement of medical products and manufacturing processes through comprehensive project management, ensuring business objectives are achieved in terms of timeline, cost, and quality.

What You'll Be Doing

• Lead and manage Margin Improvement Projects (MIP) in accordance with the plant plan and departmental commitments.
• Ensure the timely and effective implementation of assigned projects while preventing any potential impact on manufacturing lines.
• Identify opportunities for potential MIP projects through self-initiated ideas related to direct materials used in device manufacturing, including assessing feasibility, project scope, and validating the financial savings associated with the project.
• Collaborate with the Procurement department to manage material and/or product quotations as part of the evaluation and feasibility assessment of generated ideas.
• Lead and manage Workshops, Kaizen, and/or VAVE events related to idea generation for MIP projects, identifying viable opportunities and providing follow-up with cross-functional teams on generated ideas.
• Lead project planning and may direct portions of smaller projects or segments of larger projects, including scheduling, cost monitoring, resource allocation, workforce loading, and related activities.
• Develop and complete process validation activities (IQ/SV/OQ/PQ/TMV) according to project plan timelines, along with the required updates to specifications, methods, processes, or procedures that are verified or, when applicable, validated in accordance with Standard Operating Procedures (SOPs) and QSR 820.75 requirements prior to implementation.

What You'll Bring

• Bachelor's degree in Mechanical Engineering, Mechatronics Engineering, Electrical Engineering, Electromechanical Engineering, Systems Engineering, or a related field.
• Minimum of five (5) years of experience in a related position.
• Experience in problem-solving, project management and leadership, Lean practices, Six Sigma (preferred), and production line transfers.
• Experience working in ISO/FDA-regulated environments and under GMP requirements.
• Experience writing and executing process validations (IQ/SV/DOE/OQ/PQ).
• Advanced English proficiency, both written and verbal communication skills.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, let us know the nature of your request along with your contact information.

Since 1931, we have been at the forefront of innovation by bringing smarter, more personalized care to patients around the world. Now, we're more determined than ever to make a lasting impact as we are redefining healthcare delivery across the care journey. Our Mission to Save and Sustain Lives motivates us as we create a culture in which each of us can succeed. This is where you belong.