Quality Management Systems Engineer

Key Responsibilities

• Ensure QMS processes such as deviation, CAPA, change control, document control, and training are maintained in compliance with regulatory requirements and internal procedures, including management of associated electronic systems.
• Maintain and update QMS documentation, including SOPs, work instructions, and policies, ensuring they remain accurate, current, and compliant.
• Maintain control documents in eDMS, ensuring they follow the approved lifecycle and comply with established procedures.
• Serve as the business administrator for the eQMS, eDMS, and eLMS.
• Provide training and guidance to QMS end-users.
• Act as a key liaison between the QMS team and other departments to ensure on-time closure of QMS records.
• Participate in internal and external audits and support the preparation of regulatory inspection activities.
• Contribute to continuous improvement initiatives to optimize the efficiency and effectiveness of the QMS.
• Carry out other QMS responsibilities as assigned by management.

Qualifications

• Minimum of a BS, preferably in science or engineering.
• A quality assurance certification is preferred.
• Minimum 4 years of QMS activities in a bio/pharmaceutical, GxP-related Quality & Compliance environment. Device and/or biologics experience is preferred.
• Experience in GxP documentation (policies, procedures, records, etc.) and training processes.
• Experience in maintaining QMS processes (electronic & manual).
• Knowledge of computerized systems validation/ compliance.
• Proficiency with Veeva or similar electronic document management system.
• Working knowledge of learning management systems (ComplianceWire preferred).
• Proficiency in QMS platforms (Ennov preferred).
• Proficiency with data analysis tools for quality metrics (e.g., Excel, PowerBI).
• Excellent written and verbal communication skills.
• Effective organization and planning skills.

About the Role

The Quality Management Systems (QMS) Engineer is responsible for maintaining and supporting quality management systems and ensuring compliance with regulatory requirements. This role analyzes QMS data, supports audits and inspections, and collaborates with cross-functional teams to drive continuous improvement and enhance overall process effectiveness. The QMS Engineer will report directly to the Director, Quality Management Systems.

Location

Warren, New Jersey - Minimum 3 days a week on site

Pay

Salary Range: $100k - $120k

Schedule

Hybrid

Employment Type

Full-time

About DBV Technologies

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. We are on a mission to advance epicutaneous immunotherapy using our innovative technology platform, Viaskin™, to develop treatment options for immunologic diseases with significant unmet medical need. This mission drives our commitment to the advancement of treatments for patients and their families. That is why we are investigating a potential new class of immunotherapy, epicutaneous immunotherapy (EPIT), that aims to re-educate the immune system of patients through the skin. Today, we are focused on exploring the use of Viaskin to address food allergies, a devastating condition that afflicts millions of patients. As an important milestone in our journey, we hope to offer the first epicutaneous immunotherapy treatment for peanut allergy. Tomorrow, as pioneers, we will continue to explore the broad applications of this potential new class of immunotherapy, including treatments for patients suffering from inflammatory and autoimmune diseases.