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Senior Supplier Quality Engineer

DBV Technologies
Posted 3 months ago, valid for 12 days
Location

Rocky Mount, VA 24151, US

Salary

$125,000 - $150,000 per year

Contract type

Full Time

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Sonic Summary

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  • The position is for a Supplier Quality Lead in Warren, New Jersey, requiring 5-8 years of experience in Supplier Quality or Quality Engineering within the medical device or pharmaceutical industry.
  • The role involves leading supplier quality activities, supporting audits, managing CAPA, and ensuring compliance with GMP, ISO 13485, and internal standards.
  • Candidates must hold a Bachelor's degree in Engineering, Life Sciences, Pharmacy, or a related field, with a Master's preferred and formal auditor training required.
  • The salary range for this position is between $125,000 and $150,000, with a hybrid work schedule of 3 days on-site and 2 days remote.
  • Key behavioral skills sought include curiosity, courage, collaboration, and credibility to foster a positive and accountable work environment.

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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