Job Description

Akkodis is seeking a Sr. Supplier Quality Engineer for an on-site 12-month contract job with a medical device client in Jacksonville, FL. The Supplier Quality Engineer is responsible for developing and maintaining supplier quality systems, managing supplier qualifications, and supporting the approval of purchased components and materials. This role will heavily focus on PPAP (Production Part Approval Process) and other advanced quality planning tools to ensure reliable and compliant supply chain performance.

Rate Range: $52.00/hour to $55.07/hour; The rate may be negotiable based on experience, education, geographic location, and other factors.

Sr. Supplier Quality Engineer responsibilities include:

• Lead and execute PPAP submissions for new and existing components from suppliers.
• Evaluate and approve supplier processes through audits, assessments, and performance monitoring.
• Collaborate with R&D, Manufacturing, and Procurement teams during design transfer and product launch phases.
• Maintain Approved Supplier List (ASL) and supplier scorecards based on performance metrics.
• Develop and implement supplier quality agreements and corrective action plans (SCARs).
• Ensure compliance with applicable regulations (FDA, ISO 13485, MDSAP, etc.) and internal quality system requirements.
• Reviewing and assessing APQP documents including but not inclusive too: Process Flows, PFMEAs, Control Plans, Inspection Plans, MSA studies, Risk assessments, Capability, and statistical sampling plans
• Support non-conformance investigations and root cause analysis related to supplier-provided components.
• Conduct First Article Inspections (FAI) and review supplier documentation such as Certificates of Conformance, inspection reports, and process validation records.
• Drive continuous improvement initiatives within the supply chain using tools such as Six Sigma, SPC, and Lean methodologies.

Desired Qualifications:

• Bachelor’s degree in Engineering, Quality, or a related technical field.
• Minimum of 3–5 years of experience in Supplier Quality Engineering within a the medical device industry.
• Strong hands-on experience with PPAP, including understanding of all elements (e.g., PFMEA, Control Plans, MSA, Process Flow).
• Working knowledge of ISO 13485, 21 CFR Part 820, and other relevant regulatory requirements.
• Experience conducting supplier audits and performance evaluations.
• Strong problem-solving skills and familiarity with root cause analysis tools (e.g., 5 Whys, Fishbone, 8D).
• Excellent communication and interpersonal skills.

If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Stephanie.Lister@AkkodisGroup.com.

Equal Opportunity Employer/Veterans/Disabled

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client.

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

· The California Fair Chance Act

· Los Angeles City Fair Chance Ordinance

· Los Angeles County Fair Chance Ordinance for Employers

· San Francisco Fair Chance Ordinance

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