Sr Engineer - Process
Baxter International Inc.
Summary
Provide a variety of engineering work to fully support the manufacturing activities related to process and product activities, giving direct support on new product introduction, development, products and process changes, maintenance of validation program and promote continuous improvement of medical devices manufactured in Aibonito facilities. Responsible for diverse range of local and divisional project activities related to manufacturing process introduction, development and changes, maintaining the continuous improvements approach on assigned process areas to comply with establish corporate standards and Quality Regulations.
Job description
Your role at Baxter
Provide a variety of engineering work to fully support the manufacturing activities related to process and product activities, giving direct support on new product introduction, development, products and process changes, maintenance of validation program and promote continuous improvement of medical devices manufactured in Aibonito facilities. Responsible for diverse range of local and divisional project activities related to manufacturing process introduction, development and changes, maintaining the continuous improvements approach on assigned process areas to comply with establish corporate standards and Quality Regulations.
What You'll Be Doing
- Participate in multifunctional projects to contribute with plant manufacturing strategies.
- Use standard and advance engineering principles to analyze and resolve process related issues.
- Works under minimal supervision to identify manufacturing problems and respond to production requests for assistance.
- Perform and assists in the implementation of new product introductions, existing product design modifications, manufacturing improvements giving direct support on change process as change control owner and/or action owner on local or divisional projects.
- Perform and maintain process or product validations and re-validation programs using Local or Divisional engineering resources.
- Manage technical resources to clearly set workload priorities in order to effectively support the validation processes on the manufacturing areas.
- Conduct process or product transfer activities from Divisional or International facilities to the Aibonito manufacturing areas.
- Lead and supervise small project teams as needed to accomplish project objectives.
- Independently manage and perform multiple management and product engineering activities under Product Development Process guidelines.
- Give direct support during Internal, External Quality Audit processes as (MDSAP, Corporate and FDA Audits.
- Perform as Technical Approver in Aibonito on areas of responsibilities.
- Utilize and apply engineering problem solving techniques and statistical tools such as: (e.g., PFMEA, 5 Why's technique for investigations, Process Modeling, Design of Experiments, Mold Flow, SPC, etc.) during investigation and/or during process improvement process.
- Implement Value Improvement Projects by analyzing specific processes and supporting the Aibonito plant VIP program.
- Perform statistical and analytical analysis on process or product related conditions.
- Use Six-sigma engineering tools.
- Interact under minimal supervision with Divisional groups as well as other international facilities.
- Promote a zero-harm workplace, and assure that required EHS resources are available and that all applicable EHS practices and rules are being followed by supervised employees.
- Observe confidentiality and data privacy rules.
What You'll Bring
- Bachelor's degree in mechanical, Industrial, Electrical or Chemical Engineering.
- Three to Five (3-5) years related experience in manufacturing or project engineer in a closely related industry.
- Good project management and communication skills.
- Prefer experience with TQM methods (e.g. "six sigma")
- Display a solid technical understanding of engineering principles and procedures (e.g. CAD and its application or scheduling a series of technical tasks utilizing software-based tools.
- Understand and articulate how own role ties within function or discipline.
- Demonstration application of engineering principles on individual/small projects.
- Uses computer applications to do process analysis.
- Excellent problem-solving techniques.
- Excellent interpersonal skills.
- Six-sigma Engineering considered a plus.
- Knowledge of Design Control Requirements.
- Knowledge of GMP, FDA, OSHA, QLP.
- Some traveling required.
- Bilingual (Spanish and English) Oral and Writing.
- Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
Requirements
- Bachelor's degree in mechanical, Industrial, Electrical or Chemical Engineering
- Three to Five (3-5) years related experience in manufacturing or project engineer in a closely related industry
- Good project management and communication skills
- Prefer experience with TQM methods (e.g. "six sigma")
- Display a solid technical understanding of engineering principles and procedures (e.g. CAD and its application or scheduling a series of technical tasks utilizing software-based tools
- Understand and articulate how own role ties within function or discipline
- Demonstration application of engineering principles on individual/small projects
- Uses computer applications to do process analysis
- Excellent problem-solving techniques
- Excellent interpersonal skills
- Six-sigma Engineering considered a plus
- Knowledge of Design Control Requirements
- Knowledge of GMP, FDA, OSHA, QLP
- Some traveling required
- Bilingual (Spanish and English) Oral and Writing
- Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time
Benefits
- Medical, Dental & Vision
- Basic Life Insurance
- Accident Insurance
- Short-Term Disability
- Long-Term Disability
- Business Travel Accident Insurance
- Employee Stock Purchase Plan
- 401(k) Matching
- Flexible Spending Accounts
- Educational Assistance
- Paid Holidays
- Paid Time Off
- Family & Medical Leave
- Paid Parental Leave
- Commuting Benefits
- Employee Discount Program
- Employee Assistance Program
- Childcare Benefits
Company overview
Baxter International Inc. is an American multinational healthcare company headquartered in Deerfield, Illinois, founded in 1931. As a leading global medical device manufacturer, Baxter specializes in developing and producing essential medical products for treating chronic and acute medical conditions. The company operates across three primary business segments: Medical Products and Therapies, Healthcare Systems and Technologies, and Pharmaceuticals. Baxter's extensive product portfolio includes intravenous (IV) solutions, infusion pumps, dialysis equipment for kidney disease treatment, surgical technologies, and hospital pharmaceuticals. With approximately 38,000 employees worldwide and annual revenues exceeding $10 billion, Baxter plays a critical role in global healthcare infrastructure. The company is particularly known for its leadership in IV fluid production, manufacturing approximately 60% of the intravenous fluids used in the United States. Baxter's innovations include pioneering developments in artificial kidney technology and advanced surgical products, serving healthcare providers across more than 100 countries. The company maintains a strong commitment to research and development, investing significantly in medical technology advancements that improve patient outcomes and healthcare delivery efficiency.