Director, Global Product Monitoring – Post-Market Surveillance

DBV Technologies

Director of Product Monitoring & Post-Market Surveillance leading global strategy for DBV Technologies. Overseeing compliance and safety for biologics-device combination products.

Posted 5/19/2026full-timeWarren • New Jersey • 🇺🇸 United StatesLead💰 $200,000 - $235,000 per yearWebsite

Tech Stack

Tools & technologies

Assembly

About the role

Key responsibilities & impact

Develop and execute global product monitoring and PMS strategy for combination products.
Lead post-market professionals responsible for the timely and effective handling, management, preparation, and assembly of information for complaint determination, complaint evaluation, vigilance reporting, field action/recall executions and APQR management.
Comply with established global regulations and procedures for complaint and reportable event handling (post-market vigilance) to ensure timely, uniform, and accurate complaint processing and issuance of initial, supplemental, and final reports to regulatory agencies for reportable events.
Lead Annual Product Quality Reviews (APQR) and ensure integration of complaint trends, field performance, CAPA effectiveness, and stability data.
Ensure compliance with 21 CFR Part 4, 820, 211, 6xx, ISO 13485 & ISO 14971.
Collaborate cross‑functionally with Medical Affairs, Regulatory, Quality Engineering, Quality Risk Management, Operations, and other functional areas to enable and continuously improve customer experience and support improvements throughout the product lifecycle.
Conduct signal detection and trending analysis for emerging risks and ensure escalation and cross-functional engagement with stakeholders around the world to enable rapid response to emerging issues and opportunities.
This position will require approximately 20% travel to France.

Requirements

What you’ll need

Bachelor’s degree in a relevant field (e.g., engineering, life sciences, quality management) with an advanced degree preferred.
Regulatory and/or Quality Assurance certifications are a plus.
Minimum of 10 -12 years of increasing responsibility in a biotechnology/pharmaceutical, GxP-related Quality & Compliance environment.
Combination product, medical device, drug, and/or biologics experience is preferred.
Minimum 7 - 10 years direct and indirect management level experience, including senior-level project planning and working/managing in a global environment.
Experience leading complaint handling and regulatory reporting programs.
Experience in leading/managing field actions/recalls.
Deep expertise in global PMS and APQR requirements.
Strong knowledge of ISO 14971, root cause tools, and regulatory compliance.
Experience working with global teams.
Experience within 1 or more eQMS platforms for 5+ years (Veeva/ENNOV desired).

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account DBV Technologies Website LinkedIn All Job Openings 51 - 200 employees 🧬 Biotechnology 💊 Pharmaceuticals 🔥 Funding within the last year 💰 $30M Post-IPO Secondary - DBV Technologies on 2025-10 Biotechnology
Pharmaceuticals DBV Technologies is a global clinical-stage biopharmaceutical company developing epicutaneous immunotherapy to treat food allergies and other immune-mediated diseases. Founded by pediatricians, the company is advancing its proprietary VIASKIN® patch technology through clinical trials—including Phase 3 studies for a peanut allergy patch (DBV712) and earlier-stage programs for milk allergy (DBV135)—with the goal of re-educating the immune system using controlled skin exposure to antigens. Director, Global Product Monitoring – Post-Market Surveillance 🔥 0 minutes ago 🏢🏡 Warren – Hybrid 💵 $200k - $235k / year ⏰ Full Time 🔴 Lead 👔 Director Apply Now Find Hiring Managers Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
Develop and execute global product monitoring and PMS strategy for combination products.
Lead post-market professionals responsible for the timely and effective handling, management, preparation, and assembly of information for complaint determination, complaint evaluation, vigilance reporting, field action/recall executions and APQR management.
Comply with established global regulations and procedures for complaint and reportable event handling (post-market vigilance) to ensure timely, uniform, and accurate complaint processing and issuance of initial, supplemental, and final reports to regulatory agencies for reportable events.
Lead Annual Product Quality Reviews (APQR) and ensure integration of complaint trends, field performance, CAPA effectiveness, and stability data.
Ensure compliance with 21 CFR Part 4, 820, 211, 6xx, ISO 13485 & ISO 14971.
Collaborate cross‑functionally with Medical Affairs, Regulatory, Quality Engineering, Quality Risk Management, Operations, and other functional areas to enable and continuously improve customer experience and support improvements throughout the product lifecycle.
Conduct signal detection and trending analysis for emerging risks and ensure escalation and cross-functional engagement with stakeholders around the world to enable rapid response to emerging issues and opportunities.
This position will require approximately 20% travel to France. 🎯 Requirements
Bachelor’s degree in a relevant field (e.g., engineering, life sciences, quality management) with an advanced degree preferred.
Regulatory and/or Quality Assurance certifications are a plus.
Minimum of 10 -12 years of increasing responsibility in a biotechnology/pharmaceutical, GxP-related Quality & Compliance environment.
Combination product, medical device, drug, and/or biologics experience is preferred.
Minimum 7 - 10 years direct and indirect management level experience, including senior-level project planning and working/managing in a global environment.
Experience leading complaint handling and regulatory reporting programs.
Experience in leading/managing field actions/recalls.
Deep expertise in global PMS and APQR requirements.
Strong knowledge of ISO 14971, root cause tools, and regulatory compliance.
Experience working with global teams.
Experience within 1 or more eQMS platforms for 5+ years (Veeva/ENNOV desired). Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

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Hard Skills & Tools

global product monitoringpost-market vigilancecomplaint handlingregulatory reportingsignal detectiontrending analysisCAPA effectivenessPMS strategyAPQR managementroot cause analysis

Soft Skills

leadershipcross-functional collaborationproject planningcustomer experience improvementstakeholder engagementcommunicationproblem-solvingteam managementstrategic thinkingadaptability

Certifications

Regulatory certificationsQuality Assurance certifications