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Baxter International

Global provider of medical care products

Principal Engineer - Operational Excellence

Manufacturing EngineeringConfirmed live in the last 24 hours
Full-timeSkaneateles, NY, USAIn-person

About the Job

Requirements

  • A bachelor's degree in engineering, Industrial Engineering, or Manufacturing is required.
  • At least 7 years of experience in continuous improvement, process engineering, or operations management, preferably in the medical device or healthcare industry.
  • Certification in Lean Six Sigma at Black Belt or Master Black Belt level, or equivalent, is required.
  • Experience with quality management systems and regulatory requirements in the medical device industry is required.
  • Familiarity with statistical analysis software and tools such as Minitab and JMP is required.
  • Expertise in Lean Manufacturing, Six Sigma, and other continuous improvement methodologies is required.
  • Strong analytical and problem-solving skills, with a data-driven approach to decision-making, are required.
  • Project management skills and the ability to lead cross-functional teams and manage multiple projects simultaneously are required.
  • Communication skills, both verbal and written, and the ability to influence and engage stakeholders at all levels are required.
  • Applicants must be authorized to work for any employer in the United States; the employer cannot sponsor or take over sponsorship of an employment visa.

Responsibilities

  • Lead and drive continuous improvement initiatives across manufacturing and operational processes to enhance efficiency, reduce waste, and improve product quality.
  • Develop and implement continuous improvement strategies and methodologies, including Lean, Six Sigma, and other best practices, to achieve organizational goals.
  • Implement and support Lean Daily Management System processes throughout the organization.
  • Manage and oversee Operational Excellence projects from inception to completion, ensuring alignment with business objectives and timelines.
  • Collaborate with cross-functional teams to identify improvement opportunities, define project scope, and establish measurable goals.
  • Analyze operational data and performance metrics to identify trends, root causes of issues, and areas for improvement.
  • Prepare and present reports on Operational Excellence initiatives, project outcomes, and performance improvements to senior management and stakeholders.
  • Provide training and mentorship to employees on Lean and Operational Excellence methodologies, tools, and techniques to foster a culture of continuous improvement within the organization.
  • Lead workshops and Kaizen events to engage teams in problem-solving and process improvement activities.
  • Collaborate with engineering, quality assurance, production, and other departments to ensure that Operational Excellence initiatives are effectively integrated into daily operations.
  • Communicate with stakeholders at all levels, providing updates on Operational Excellence projects, challenges, and successes.
  • Ensure that all continuous improvement activities comply with relevant regulatory standards and quality management systems, including FDA requirements and ISO 13485.
  • Work closely with regulatory affairs teams to support compliance efforts related to continuous improvement initiatives.
  • Stay up to date with industry trends, emerging technologies, and best practices in continuous improvement and manufacturing processes.
  • Identify and implement innovative solutions to enhance operational performance and drive competitive advantage.
  • Perform other duties assigned by management to support the overall goals of the continuous improvement team.
  • Contribute proactively to zero harm in the workplace by complying with legal and corporate Environmental Health and Safety requirements, safe work practices, and Environmental Health and Safety policies and procedures.
  • Report hazards, near misses, and incidents as soon as practicable, and participate in identifying actions to prevent harm to employees and the environment.
  • Contribute to Good Manufacturing Practices and regulatory performance in the department to ensure the quality program is met.
  • Ensure compliance with FDA, ISO, and other government regulations, legal documents, and safety and ethical standards, and complete legal compliance training.

Desired Qualifications

  • A master's degree is preferred.
  • Experience in the medical device or healthcare industry is preferred.

About the Company

Baxter International

Global provider of medical care products

Baxter International develops and manufactures medical products and equipment for hospitals and blood banks. Its products include sterile IV solutions and blood storage containers; innovations like the Transfuso-Vac extended blood shelf life, and a plastic blood bag helped shape modern blood banking. The company differs from competitors through a long track record of sterile manufacturing, blood-storage innovations, and strategic mergers that broaden its product portfolio. Its goal is to provide reliable, safe medical products that support patient care and hospital operations worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Deerfield, IL
Founded
1931

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