Siemens Manufacturing Industrial Engineer, Sr in Mishawaka, Indiana

Manufacturing Industrial Engineer, Sr

Locations:Mishawaka, Indiana

Job Family: Manufacturing

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Job Description

Division: Siemens Healthineers

Business Unit: Point of Care

Requisition Number: 200116

Assignment Category: Full-time regular

Experience Level: Senior level

Education Required Level: Bachelor's Degree

Travel Required: 5%

Division Description:

Siemens is a global technology powerhouse that has stood for engineering excellence, innovation, quality, reliability and internationality for more than 165 years. As a global technology company, Siemens is rigorously leveraging the advantages that this setup provides. To tap business opportunities in both new and established markets, the Company is organized in nine Divisions: Power and Gas, Wind Power and Renewables, Energy Management, Building Technologies, Mobility, Digital Factory, Process Industries and Drives, Healthineers and Financial Services.

With 45,000 employees Siemens Healthineers is one of the world’s largest suppliers of technology to the healthcare industry and a leader in medical imaging, laboratory diagnostics and healthcare IT. All supported by a comprehensive portfolio of clinical consulting, training, and services available across the globe and tailored to customers’ needs. So that more people can have a life that is longer, richer, and more filled with happiness.

For more information, please visit: http://www.usa.siemens.com/healthineers

Job Description:

Supports the plant manufacturing effort, with proven ability to identify problems and pursue plans toward their resolution. Specific focus will be in areas of improving chronic issues related to quality, waste and equipment efficiency

• Technical work may be complex and difficult to relate to existing technologies, requiring broad application of knowledge and principles

• Demonstrated innovation, creativity and problem solving skills in a fast paced, global environment.

• Experience with multiple manufacturing processes (i.e. PLC Automated Equipment, Thermal Heat Sealing, Ultrasonic Welding, Dispense System, Pneumatics etc.)

• Capable creating designs of parts and mechanical subassemblies using in-depth knowledge of materials and processes to meet extremely challenging technical requirements.

• Responsible for the Environmental and Health & Safety effects of the work performed

• Keep up to date on new developments and technologies in assigned disciplines and present on new ‘Best Practice’ methodologies, procedures, processes and equipment to the company in a proactive manner.

• Engage with the appropriate personnel in the identification and resolution of Corrective/Preventative actions to address Quality, Technical, and Manufacturing issues (Audit Actions, NCR’s, CAPA’s, etc).

• Responsible for identification and implementation of equipment related continuous improvement activities to improve product quality and increase Overall Equipment Effectiveness.

• Responsible for all associated documentation, including but not limited to, the following: Validations, Standard Operating Procedures, Preventive Maintenance Schedules, Engineering Change Notifications, Spare Parts Listings, etc. in line with FDA regulations.

Required Knowledge/Skills, Education, and Experience

  • BS degree or equivalent experience (i.e. Electrical, Software discplines)

  • 5 - 8 years of relevant experience

  • Experience with multiple manufacturing processes (i.e. PLC Automated Equipment, Thermal Heat Sealing, Ultrasonic Welding, Dispense System, Pneumatics etc.)

  • Strong trouble-shooting , design and programming skills for PLC's

  • Experience troubleshooting automated industrial production equipment

Preferred Knowledge/ Skills, Education and Experience

  • Experience with vision systems(i.e.Cognex)

  • Previous work experience in IQ/OQ/PQ and Process Validation protocols for Quality System (QS) Regulation/Medical Device Good Manufacturing Practices within an FDA regulated environment that is ISO certified.

Required Knowledge/Skills, Education, and Experience

  • BS degree in Engineering (i.e. Mechanical; Industrial Automation Engineering, etc.) or equivalent education & experience

  • 5 - 8 years of relevant experience

  • Experience troubleshooting automated industrial production equipment

  • Experience supporting highly automated production lines

  • CAD experience

Preferred Knowledge/ Skills, Education and Experience

  • Experience with vision systems(i.e.Cognex)

  • Previous work experience in IQ/OQ/PQ and Process Validation protocols for Quality System (QS) Regulation/Medical Device /Good Manufacturing Practices within an FDA regulated environment

*LI-EMM

Equal Employment Opportunity Statement

Siemens is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, protected veteran or military status, and other categories protected by federal, state or local law.

EEO is the Law

Applicants and employees are protected under Federal law from discrimination. To learn more, Click here at https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm .

Pay Transparency Non-Discrimination Provision

Siemens follows Executive Order 11246, including the Pay Transparency Nondiscrimination Provision. To learn more, Click here at https://www.dol.gov/ofccp/pdf/PayTransparencyNotice_JRFQA508c.pdf .