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Senior Supplier Quality Engineer

Job in Bernards Township, Somerset County, New Jersey, USA
Listing for: DBV Technologies
Full Time position
Listed on 2026-05-21
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Description:

Lead supplier quality activities to ensure externally supplied materials, components, and services meet GMP, ISO 13485, and internal standards. Support the audit program, CAPA follow-up, and Quality Technical Agreements (QTAs) in partnership with Supplier Owner and cross-functional teams.

Location: Warren, New Jersey - 3 days on site & 2 days remote

Salary Range
: 125k-150k

Key Responsibilities:
  • Support the audit program: annual plan, execution, reporting, and follow-up of CAPA effectiveness.
  • Maintain supplier risk assessment, segmentation, and performance reviews; drive improvement actions with suppliers.
  • Lead QTA lifecycle: creation, review, negotiation support with Procurement, and periodic updates; ensure RACI is defined and applied.
  • Support SOPs for Supplier Management and ensure alignment with global procedures, coach teams on process adherence.
  • Ensure readiness for inspections (e.g., FDA, EU) and PAI: maintain supplier files GMP certificates, monitor expirations, and prepare audit/inspection evidence.
  • Provide quality engineering support (incoming controls, sampling plans, problem solving 8D/5

    Why, data analysis) to prevent recurrence of issues.
Qualifications:
  • Bachelor’s degree in Engineering, Life Sciences, Pharmacy or related field (Master’s preferred).
  • Formal auditor training (ISO 13485, GMP) required or equivalent experience;
    Lead Auditor certification preferred.
  • 5–8 years in Supplier Quality/Quality Engineering in medical device and/or pharma.
    Pharma/Biologics preferred.
  • Proven experience leading supplier audits, managing CAPA, and implementing QTAs.
  • Working knowledge of FDA 21 CFR Parts 820/210/211/600/610/680, EU GMP, ISO 13485, ISO 14971.
  • Experience with eQMS (Veeva or ENNOV is a +), supplier performance dashboards, and RACI implementation.
  • Fluent in English; strong communication and stakeholder influencing skills.
Behavioral

Skills:
  • Curiosity:
    Keep on exploring uncharted territories. Always ask “why?” and more importantly “why not?”
  • Courage:
    Take smart risks, mentor each other to always do better & be accountable for our choices, our opinions, and our actions.
  • Collaboration:

    Teamwork and spirit. Support each other and be equally involved in the achievement of our common goals.
  • Credibility:
    Be transparent, follow through and build trust. Educate ourselves about our unique technology.
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Position Requirements
10+ Years work experience
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