Global Supplier Quality ASL and Supplier Performance Manager

Job Title

Job Description

Global Supplier Quality ASL and Supplier Performance Manager

The Global Supplier Quality ASL and Supplier Performance Manager is responsible for global governance execution global process ownership and continuous improvement of supplier quality management activities within a regulated medical device environment. This role has end to end ownership of the Approved Supplier List (ASL) Supplier Performance Monitoring Supplier Corrective Action Requests (SCARs) and Supplier Quality Agreements.

Your role:

• Global Supplier Quality Governance & Operations: Manage the global Approved Supplier List (ASL) oversee supplier performance monitoring and drive corrective actions and continuous improvement with suppliers and stakeholders.
• Process Ownership & Continuous Improvement: Lead and enhance supplier quality processes standardize procedures and tools define KPIs and ensuring alignment with business needs and regulatory requirements.
• Supplier Quality Agreements: Develop negotiate and maintain Supplier Quality Agreements to clearly define quality roles regulatory expectations and ensure alignment with internal systems.
• Compliance Audits & Regulatory Support: Ensure supplier quality processes comply with FDA ISO and international standards support audits and inspections and serve as subject matter expert in supplier quality management.
• Cross-Functional & Global Collaboration: Collaborate with Procurement Regulatory Affairs and Quality teams providing training and support to regional and functional groups for effective supplier quality management.

Youre the right fit if:

• Youve acquired 10 years of experience with Bachelors or Minimum 7 years of experience with Masters in areas such as Quality Engineering Safety Engineering Process Engineering Continuous Improvement Techniques or equivalent. Demonstrated experience managing Approved Supplier Lists and supplier performance programs and proven experience owning and governing quality processes at a global or enterprise level required. Experience working in a global matrixed organization and experience with supplier risk management frameworks and performance analytics preferred.
• Your skills include strong working knowledge of FDA QSR ISO 13845 and global medical device regulatory requirements; and strong analytical problem-solving communication and stakeholder management skills.
• You have a bachelors degree in engineering Quality Supply Chain or a related discipline required masters degree preferred. ASQ CQE CQA CQM or equivalent certifications preferred.
• You must be able to successfully perform the following minimum Physical Cognitive and Environmental job requirements with or without accommodation for this position.
• You have a proven track record of Supplier Performance Management Cross-Functional Leadership Process Ownership & Standardization Global Supplier Quality Governance Regulatory & Compliance Expertise and Risk-Based Decision Making.

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 companys facilities. Field roles are most effectively done outside of the companys main facilities generally at the customers or suppliers locations.

This is an office-based role.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters and we wont stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
• Learn more about our culture.

Philips Transparency Details

The pay range for this position in Colorado Springs CO Latham NY Murrysville PA Nashville TN Orange Village OH and Reedsville PA is $117000 to $186000.

The pay range for this position in Malvern PA and Plymouth MN is $123000 to $195000.

The pay range for this position in Bothell WA Cambridge MA and San Diego CA is $131000 to $208000.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills experience business needs geographical location and internal equity.

In addition other compensation such as an annual incentive bonus sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program which includes a generous PTO 401k (up to 7% match) HSA (with company contribution) stock purchase plan education reimbursement and much more. Details about our benefits can be found here.

At Philips it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.

Additional Information

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa now or in the future.

Company relocation benefits will not be provided for this position. For this position you must reside in or within commuting distance to posted location.

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This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.