Director of Regulatory Affairs

Nova Pneuma, Inc., a wholly owned subsidiary of Lee’s Pharmaceutical Holdings Limited
, is a clinical-stage biotechnology company focused on developing and commercializing innovative therapies for the acute treatment of serious medical conditions—where rapid therapeutic effect can make a meaningful difference for patients.

Our team is driven by urgency, scientific rigor, and the conviction that innovation must translate into real-world benefit—simple, fast, and patient-friendly solutions that redefine how acute conditions are treated.

Manages all regulatory activities for the company. Develops and implements regulatory strategies for internal product development. Works with partners representing company’s interests and support partners’ filing and regulatory activities. Provides counsel to other R&D and Commercial product team members. Ensures timely preparation of organized and scientifically valid regulatory documents and submissions. Provides expertise in translating regulatory requirements into practical, workable plans.

Contact person for regulatory agencies. Manages regulatory document system, including the archival storage and protection of regulatory filings.

• Develop and implement regulatory strategies for successful submission of product candidates from pre-IND stage through the product approval process.
• Collaborate with project teams to ensure regulatory compliance throughout the product development and product lifecycle.
• Direct regulatory activities for maintenance and continued compliance of commercial product(s).
• Serve as the liaison for regulatory authorities.
• Work with partners on their regulatory submissions, including attendance of recurring meetings and document preparation for sections that the company is responsible for
• Act as company PV/Drug Safety representative and point of contact with external partners.
• Provide leadership to direct report(s) and regulatory guidance to project teams
• Prepare regulatory submissions (e.g. IND, NDA, Technical File) by coordinating work cross functionally on data requirements to create content with in a timely manner.
• Develop sound internal policies, standards and strategies related to submissions and identify risks associated with that strategy.
• Review and approve regulatory submission documents to ensure compliance with industry and regulatory standards.
• Maintain IND, NDA, and other regulatory submission documents including tracking of all regulatory interactions.
• Manage and prepare post-market filings and product safety reports (e.g., Annual Reports, DSUR, PSUR, REMS Annual Report, Supplements, Technical Documentation File lifecycle maintenance, responses to regulatory information requests).
• Provide regular updates and progress reports to the Executive Team and project teams.
• Establish and maintain regulatory SOPs.
• Regulatory surveillance and monitoring to ensure compliance with current regulations. Work with SMEs to assess impact of new or revised regulations to procedures and programs.

• Previous work with FDA on regulatory submissions (work with EMA, CDE, Notified Body, etc. is a plus)
• Must have IND filing experience and regulatory submissions related to clinical studies; direct regulatory experience supporting commercial products (NDA experience) is a plus
• Experience with drug safety and pharmacovigilance is preferred
• Hands-on experience preparing domestic and international regulatory submissions, ideally for both pharmaceutical drug-device combination products and medical devices.
• Excellent written and verbal communication skills for effective communication of complex regulatory issues.
• Effectively communicate risks/benefits of available options to address such complex issues.
• Excellent organizational…