Supplier Quality Engineer

Philips Iberica SAU; Bedford (MA); On-site; USD 103,000 - 163,000; Full time

Job summary

Philips Iberica SAU is seeking a Supplier Quality Engineer in Bedford, MA. This role involves driving supplier performance and ensuring product quality. Candidates should have significant experience in FDA regulated environments, strong communication skills, and a Bachelor’s degree in Quality or Engineering.

The position offers a competitive salary range of $103,000 to $163,000 depending on experience and qualifications.

Qualifications

• 5+ years’ experience in Supplier Quality Engineering within FDA regulated environments.
• Detailed knowledge of medical device regulations and standards.
• Experience using data analytics to assess supplier performance.

Responsibilities

• Coordinate supplier improvement initiatives and manage Supplier Quality Agreements.
• Monitor product/process quality and troubleshoot production issues.
• Conduct audits and manage planning, execution, and reporting.

Skills

Supplier Quality Engineering

Data analytics

Communication skills

Process improvement

Education

Bachelor’s Degree in Quality, Engineering, or related disciplines

Tools

Data analytics tools

Job description

Job Title

Supplier Quality Engineer

Job Description

The Supplier Quality Engineer is a key member of Philips’ Image Guided Therapy Devices (IGTD) Quality team, responsible for driving supplier performance and continuous/process improvement, striving for continuous quality improvement throughout the product lifecycle, and ensuring regulatory compliance.

Your role:

• Coordinates and executes supplier improvement initiatives, managing the Approved Supplier List and negotiating Supplier Quality Agreements.
• Provide sustaining SQE activities in managing daily NCR's, SCAR's, SCN's, and the ASL. Manage APQP with selected suppliers.
• Facilitates technical capability assessments of potential new suppliers, ensuring they meet the company's quality standards, and contributes to the supplier selection.
• Proactively monitoring and measuring product/process quality and performance trends and troubleshooting of production/release issues.
• Assists with the process of making additions, changes, or deletions to the Approved Supplier List, ensuring that only qualified suppliers are retained.
• Supports in end-to-end performance management of suppliers, conducts detailed analysis of defects to determine if they are supplier-caused, and acts as an independent reviewer for Supplier Corrective Action Requests.
• Proactively monitoring and measuring product/process quality and performance trends and troubleshooting of production/release issues.
• Develop and oversee equipment qualification and process validation plans and lead continuous improvement projects based on process/product trends, customer complaints, industry standards and government regulations.
• Provide Quality oversight of product/process change requests from suppliers, ensuring appropriate regulatory review and adequate validation to support requested changes.
• Drive supplier improvement, corrective and corrective actions (SCARS).
• Serve as internal and supplier quality auditor, managing planning, execution, reporting and closure of audits and audit findings.

You're the right fit if:

• You have a minimum of 5+ years’ experience in Supplier Quality Engineering within FDA regulated medical device environments, with a focus on supplier selection, performance assessment, APQP, Risk Assessments/PFMEA’s, SPC, SCAR’s, SICR, CAPA, Remediation etc.
• You have detailed knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts 803, 806, and 820, ISO 13485, ISO 14971, European Medical Device Directive (93/42/EEC), EU Medical Device Regulation, Canadian Medical Devices Regulation (SOR/98-282). You have proven experience utilizing data analytics/KPI’s to assess supplier performance and identify/drive process improvement opportunities.
• You have strong communications skills and the proven ability to effectively communicate, influence and build relationships cross-functionally with a variety of internal/external stakeholders, suppliers, Regulatory Agencies, Notified Bodies etc.
• You have a minimum of a Bachelor’s Degree (Required) in Quality, Engineering, or related disciplines. ASQ and/or Six Sigma DfX Certifications-Desired.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

How we work together:

We believe that we are better together than a part. 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. This is an Office-based role.

Pay range

The pay range for this position in Bedford, MA is $103,000 to $163,000. 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.

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 Bedford, MA.
• This role may require travel up to 10%.

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