**This is where you save and sustain lives**
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
As a Manufacturing Engineer you will perform various engineering and leadership duties in support of manufacturing operation processes, to ensure a safety environment for operator to achieve daily production targets in compliance with the Baxter quality system. You will also have responsibility over product transfers and NPI support and VIP projects. You will be working side by side with experienced engineers. You will work in a multi-disciplinary engineering environment as well as gain knowledge of other fields that support a manufacturing environment.
Thisiswhere your expertise save lives.
**Your team**:
You will be part of a collaborative engineering team that is experienced in manufacturing engineering. We support a culture where everyone works together to meet deadlines, achieve goals and ultimately Save and Sustain Lives
**What you´ll be doing**:
- Develop and implement manufacturing processes for mainly existing products, including operation sequence, machinery, tools and equipment requirements, cost estimates and return on investment analysis, with the objective of achieve the targets of productivity and efficiency of the process.
- Manage the implementation of changes in product design and process changes through fabrication, purchasing of equipment, tooling, fixtures, and assembly process.
- Responsible for total product quality, which may include the ownership of solving quality problems using the NCR, NCMR, A3´s or other problem-solving methodology, execute processes validation and qualification, develop, and implement process controls using statistical techniques.
- Responsible to document and keep up to date the job Instructions, visual aids, process related quality system procedures and personnel training and certification, as well as labor standards and routings.
- Responsible for ensuring manufacturing processes are compliant with FDA Quality System Regulation as well as Baxter Quality System Requirements.
- Drive continuous improvement and lean manufacturing methodologies into the manufacturing process including material flow and line balancing to meet required production rates, labor and equipment capacity analisys.
- Responsible for EHS compliance, this means, execute projects to improve ergonomics in each work station to prevent injury
**What you´ll bring**:
- Bachelor of Mechanical Engineering, Electronic, Industrial or equivalent
- Minimum of 3 years of experience in related field
- Bilingual English-Spanish
- Excellent analytical decision making and problem-solving skills.
- AutoCAD
- Validation process for the medical industries
- PFMEA, control plan, diagram flow
- Line balancing (Takt Time, cycle time)
- Six sigma, and lean manufacturing
- Statistical analysis for processes (CpK, PpK, CP, normal and non-normal distributions, P-Value)
- Design of experiments (DOE)
**Reasonable Accommodations**
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