**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.
JOB SUMMARY:
Perform various engineering, leadership duties in support of operation processes, in order to achieve the daily goals in terms of EHS and Quality compliance as well as Productivity.
The Manufacturing Process Engineer is responsible to improve their assigned lines to meet the productivity requirements in agreement with Baxter's Key Performance Metrics, he is also responsible to optimize the product Flow of the Lines and implement the change requirements via SUS, MODs, NCMRs, CAPAs, etc.
The Manufacturing Process Engineer requires technical skills and knowledge, Experience of any industry in Mechanical, Hydraulic, Mechanical, Pneumatic and Problem Solving.
Excellent knowledge on preventive, corrective and predictive maintenance.
Build a positive and productive relationship with all members of the maintenance Team.
foster a culture of innovation and continues improvement
ESSENTIAL DUTIES AND RESPONSIBILITIES: - Other duties may be assigned:
- Execute and document the evidence of the monitoring and control activities of the manufacturing process, in order to sustain quality levels and EHS requirements for every day's production.
- Establishment of the manufacturing sequence to achieve production goals daily.
- Responsible for the quality of the operation product process, which may include the ownership of resolving quality problems using the CAPA methodology, execute processes validation and qualification, develop and implement process controls using statistical techniques such as design of experiments.
- Responsible to document and keep up to date the job Instructions, visual aids, and related quality system procedures.
- Manage the implementation of product changes through fabrication, purchasing, and assembly due to engineering changes and new product instructions.
- Drive continuous improvement and lean manufacturing methodologies into the manufacturing process including material flow and line balancing, workstation arrangements to meet required production rates and improve efficiency of the painting process.
- Responsible for EHS compliance in their assigned lines, this means, execute projects to improve ergonomics in each workstation to prevent injury.
- Design and validate the DHRs for the parts or product he/she is responsible for.
- Able to enter Information and modify Routings and BOMs on JDE
- Responsible for ensuring that our manufacturing processes compliant with FDA Quality System Regulation as well as Baxter Quality System Requirements.
- Responsible for leading teams and directing the technical efforts of others.
- Promote core Baxter behaviors and values.
- Create and continuously improve the systems for the elimination of downtime in manufacturing areas.
- Support the manufacturing process, with projects to improve the Quality, Cost and Lean manufacturing.
- Support manufacturing in the installation of new process equipment.
- Comply & provide all Corporate Requirements.
- Lead Planning & coordination of EHS training.
- Develop & implement programs & practices to assure 100% compliance with applicable Federal, State, Local and Baxter regulations & practices.
- Participate in Lean Manufacturing Initiatives.
- Coordinate and supervise the design, construction, and assembly of machinery.
- Comply with the safety regulations established in the organization.
EDUCATION, EXPERIENCE AND QUALIFICATIONS:
- 5 to 8 years of experience in manufacturing process, medical field desirable.
- Strong teamwork and communication skills which are effective in cross-functional teams as a leader or member.
- Experience with Manufacturing process engineer activities, programming, rack design, line balancing, time studies.
- Experience working with vendors, suppliers and contractors.
- Ability to manage complete project cycle from concept to actual implementation.
- Excellent analytical decision making and problem-solving skills.
- Bilingual English / Spanish.
- Bachelor of Engineering preferred.
**Reasonable Accommodations**
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