Manager, Regulatory Affairs Operations

DBV Technologies; New Jersey; On-site; USD 125,000 - 160,000; Full time

Job summary

DBV Technologies is seeking a Manager Regulatory Affairs Operations to support regulatory submissions to global health authorities, with a strong focus on U.S. FDA filings. The role collaborates cross-functionally to ensure timely, compliant submissions (BLA/IND) and maintains submission plans, timelines, and content.

Location is Warren, NJ (3 days on site) with a salary range of $125–160K. The incumbent will lead coordination, publishing, and quality control activities and help optimize RIMS

Qualifications

• Bachelor's degree in biochemistry, chemistry, biology, or a related pharmaceutical field is required.
• An advanced degree (PhD, PharmD, MS) is strongly preferred.
• Minimum of 3-5 years regulatory experience in biotech/pharma, with biologics focus preferred.
• Experience supporting U.S. FDA submissions (BLA/IND) and eCTD requirements.

Responsibilities

• Develop and manage submission content plans and timelines.
• Lead coordination of regulatory submissions including BLAs and INDs.
• Collaborate with cross-functional teams to align submission content.
• Oversee QC activities to ensure accuracy and regulatory compliance.
• Manage RIMS records and support Veeva RIM adoption.
• Monitor regulatory changes and communicate implications to stakeholders.
• Support vendor management and contract administration.

Skills

Attention to detail

Project management

Cross-functional collaboration

Regulatory knowledge

FDA submission expertise

Education

Bachelor's degree in biochemistry/related

Advanced degree preferred (PhD/PharmD/MS)

Tools

Veeva RIM

eCTD knowledge

ePublishing processes

Regulatory information systems

Job description

Description :

The Manager Regulatory Affairs Operations is responsible for supporting the preparation, coordination, and submission of regulatory filings to global health authorities, with a strong focus on U.S. FDA submissions. This role collaborates closely with Regulatory Affairs and cross-functional teams to ensure the timely and compliant delivery of high-quality regulatory submissions, including major marketing applications (e.g., BLAs) and investigational applications (e.g., INDs).

Key responsibilities include developing and managing submission content plans, preparing regulatory submission documents (e.g., cover letters, FDA Forms), overseeing submission timelines, and coordinating publishing activities. The role requires a highly detail-oriented, proactive individual who can effectively manage multiple priorities in a fast-paced environment.

Location :Warren, New Jersey - 3 days on site

Salary Range :$125-160K

Key Responsibilities :

Regulatory Submission Planning & Strategy

Collaborate with cross-functional teams to develop and maintain comprehensive global submission content plans, including dossier structure, key deliverables, timelines, and projected approval milestones.

Conduct scenario planning to evaluate alternative regulatory strategies and recommend approaches to optimize submission timelines and mitigate risks.

Regulatory Submissions Coordination

Lead the coordination and execution of regulatory submissions, including BLAs, INDs, and responses to Health Authority requests.

Partner with functional teams (CMC, Nonclinical, Clinical, Labeling, and others) to ensure alignment on submission content and timelines.

Support the preparation, submission, and defense of major U.S. marketing applications (e.g., BLA).

Submission Quality Control

Participate in and/or lead quality control (QC) activities for regulatory submissions to ensure accuracy, completeness, and compliance with regulatory requirements (e.g., eCTD standards).

Ensure all submission components meet internal quality standards and are delivered within established timelines.

Regulatory Information Management Systems (RIMS)

Manage regulatory submission records, documentation, and archiving within the Regulatory Information Management System (RIMS) for assigned programs.

Support the organization’s transition to and optimization of Veeva RIM, including process alignment and user adoption.

Regulatory Intelligence

Monitor evolving regulatory requirements and industry trends, particularly related to ePublishing and submission standards.

Assess potential impact of regulatory changes on ongoing and planned submissions and communicate implications to stakeholders.

Vendor & Contract Management

Support management of external vendors, including ePublishing providers and other regulatory service partners.

Assist with contract administration, including creation and tracking of purchase orders and budget monitoring.

Qualifications :

Bachelor’s degree in biochemistry, chemistry, biology, or a related pharmaceutical field is required; an advanced degree (PhD, PharmD, MS) is strongly preferred.

Minimum of 3-5 years of regulatory experience in the biotech or pharmaceutical industry, with a focus on biologics, is strongly preferred.

Experience supporting U.S. FDA submissions (e.g., BLA, IND) and strong understanding of eCTD requirements.

Demonstrated experience in submission planning, coordination, and lifecycle management.

Must have experience with Regulatory Information Management Systems Veeva RIM

Knowledgeable with ePublishing processes and vendor coordination.

Strong attention to detail, organization, and project management skills.

Ability to manage multiple complex projects with competing deadlines.

Proactive mindset with strong problem-solving capabilities.

Excellent communication and cross-functional collaboration 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.