Supplier Quality Engineer

Job Title

Job Description

Job Title : Supplier Quality Engineer

Job Responsibilities:

• Process Validation for FDA remediation, who has hands on experience on non-verifiable manufacturing processes, APQP, Process validations and good communication and negotiation skills.

. Evaluates potential new suppliers through technical capability assessments, ensuring they meet the company's rigorous standards and can deliver high-quality components and assists in the supplier selection.
. Executes DFMAT (Design for Manufacturing and Assembly Technique), SAF (Supplier Approval Form), MSA (Measurement System Analysis), PFMEA (Process Failure Mode and Effects Analysis), Control Plan, SPC (Statistical Process Control), PV&V (Process Validation and Verification), FAI (First Article Inspection), LRA (Logistics Risk Assessment), and SICR (Supplier Initiated Change Request).
. Executes, monitors, and controls APQP (Advanced Product Quality Planning) processes during NPI projects to maintain consistent quality and adherence to project timelines.
. Contributes to the Supplier Project Book by documenting detailed quality requirements and expectations for suppliers, ensuring clear communication and compliance.
. Facilitates Design for Excellence (DfX) collaboration between R&D and suppliers to enhance product design quality, leveraging supplier expertise for better design outcomes.
. Ensures Critical to Quality (CtQ) characteristics are clearly communicated to suppliers and rigorously maintained throughout the production process, securing consistent product quality.
. Executes Part Submission Warrant plans, deliverables, line releases, and completion, ensuring that all parts meet specified quality standards before they are approved for use.
. Supports supplier improvement and development on APQP, providing guidance and resources to help suppliers enhance their quality processes and achieve compliance.
. Reviews Supplier Agreements, conducts thorough analysis of defects to determine if they are supplier-caused, and coordinates Supplier Corrective Action Requests to address and resolve quality issues effectively.

Minimum required Education:
Bachelor's Degree in Engineering Science, Supply Chain Management, Electrical Engineering, Electronic Engineering or equivalent.

Minimum required Experience:
Minimum 5-6 years of experience in Quality Engineering, Process Engineering, Continuous Improvement Techniques in a Medtech Industry

Preferred Education:

Bachelor's Degree in Engineering Science, Mechanical, Electrical Engineering, Electronic Engineering.

Preferred Experience:

5-6 years of experience

Preferred Skills:

Process Validation and Verification (PV&V)
. Supplier Quality Management
. Quality Management Procedures and Methodologies
. Supplier Evaluation Methodologies
. Data Analysis & Interpretation
. DfX Methodology
. Supply Chain Management (SCM)
. Quality Specifications
. CAPA Methodologies
. Statistical Process Control (SPC)
. Measurement Systems Analysis (MSA)
. First Article Inspections
. Documentation & Reporting
. Continuous Improvement

How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company's facilities.
Field roles are most effectively done outside of the company's main facilities, generally at the customers or suppliers locations.
Indicate if this role is an office/field/onsite role.

About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .