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Location
In office
Seniority
Senior · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Sep 29, 2026. First seen by Alion on May 13, 2026.

Overview
Company
Impact
Profile match
DBV Technologies is a global clinical stage biopharmaceutical company founded by pediatricians who believed that food allergies could one day be treated safely and effectively.

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 -Minimum 3 days a week on site

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/5Why, 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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