Philips
NL-MF
Posted
Feb 5, 2025
Project ID:
PHIAJP00001641
Location
Best
Hours/week
40 hrs/week
Timeline
1 year
Starts: Feb 1, 2025
Ends: Jan 31, 2026
Payrate range
Unknown
Application Deadline: Feb 1, 2025 12:00 PM
Manufacturing Engineer IGT Process Validation (m/f/d)
Environment:
The Manufacturing Engineer you responsible for giving support, improve and maintain the production process within the Manufacturing Department Factory Best.
This role is in the IGT Factory and will be responsible for raising the bar in our Quality journey.
Being part of Factory Best, one of the largest Medical Manufacturing Sites in Health Systems. Your part of Manufacturing Engineering, a team which is responsible for processes within: Imaging Guide Therapy (IGT); Magnetic resonance imaging (MR); Service, Parts & Repair (SP&R); Imaging Components (IC); Refurbishment System (RS); Digital X-Ray (DXR); Parts Recovery (PR). Working closely with operations, quality and development.
Responsibility:
within IGT:
- Analysis of performance data with respect to products and processes (Six-sigma, Statistical Process Control).
- Releases and validates new & existing processes.
- Provides structural solutions by initiating amendments like problem reports (PR) and/or 8D forms (Problem Solving methodology), including the required implementation of manufacturing process change.
- Participates as process validation expert in audits
Requirements:
- Typical bachelor or master in BioMedical Engineering, Applied Physics, or comparable.
- Proficient in documentation and natural inclination for accuracy.
- Be independent, pro-active, and not afraid to take ownership, including relevant stakeholders? management.
- A result & quality driven approach.
- Preferable experience with Process Validation or background in Quality.
- ? 2 years of experience within Manufacturing or Engineering within high tech industry.
- Comprehension skills and ability to analyze and summarize.
- Experience with quality management and quality systems. Preferably experience in the medical industry (ISO 9001, 13485, FDA requirements, audits, FMEA, 8D, SPC, etc.).
- Human & communication skills. Communication with operators up to developers & management
Working at Philips is more than a job. It?s a calling to create a healthier society through meaningful work, focused on innovative, customer-first health technology solutions. Help us improve the health and well-being of billions of people, every year. Ultimately creating a career that no one could have planned for.
Environment:
The Manufacturing Engineer you responsible for giving support, improve and maintain the production process within the Manufacturing Department Factory Best.
This role is in the IGT Factory and will be responsible for raising the bar in our Quality journey.
Being part of Factory Best, one of the largest Medical Manufacturing Sites in Health Systems. Your part of Manufacturing Engineering, a team which is responsible for processes within: Imaging Guide Therapy (IGT); Magnetic resonance imaging (MR); Service, Parts & Repair (SP&R); Imaging Components (IC); Refurbishment System (RS); Digital X-Ray (DXR); Parts Recovery (PR). Working closely with operations, quality and development.
Responsibility:
within IGT:
- Analysis of performance data with respect to products and processes (Six-sigma, Statistical Process Control).
- Releases and validates new & existing processes.
- Provides structural solutions by initiating amendments like problem reports (PR) and/or 8D forms (Problem Solving methodology), including the required implementation of manufacturing process change.
- Participates as process validation expert in audits
Requirements:
- Typical bachelor or master in BioMedical Engineering, Applied Physics, or comparable.
- Proficient in documentation and natural inclination for accuracy.
- Be independent, pro-active, and not afraid to take ownership, including relevant stakeholders? management.
- A result & quality driven approach.
- Preferable experience with Process Validation or background in Quality.
- ? 2 years of experience within Manufacturing or Engineering within high tech industry.
- Comprehension skills and ability to analyze and summarize.
- Experience with quality management and quality systems. Preferably experience in the medical industry (ISO 9001, 13485, FDA requirements, audits, FMEA, 8D, SPC, etc.).
- Human & communication skills. Communication with operators up to developers & management
Working at Philips is more than a job. It?s a calling to create a healthier society through meaningful work, focused on innovative, customer-first health technology solutions. Help us improve the health and well-being of billions of people, every year. Ultimately creating a career that no one could have planned for.
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