Director, Regulatory Affairs, US

Come and Save Lives with Us!

SERB Pharmaceuticals is a growing international specialty pharmaceutical group that is a dedicated ally to healthcare providers treating patients with critical conditions, focusing on emergency care and rare diseases.  We have over 470 employees in 16 countries and a group revenue in excess of €350m.

Our portfolio 80+ rescue medicines make a real difference in the lives of patients and their caregivers and that gives every one of our employees a sense of purpose.

Our Purpose is supported by our 4 key values:

• We make patients our priority
• We act with integrity and accountability        
• We work together as one team         
• We look for better ways forward       

Broad Overview

The Director of Regulatory Affairs (U.S.) will be responsible for leading the regulatory strategy and overseeing all regulatory activities for the company's U.S. operations. This individual will lead US regulatory affairs professionals and work closely with the Global Regulatory Affairs team and cross functionally teams. This individual will report into our Head of Global Regulatory Affairs offering a range of support as required with a focus on Regulatory Advertising, Promotion and labeling activities.

 

In this role, the individual will drive regulatory strategies and labelling product compliance initiatives to support FDA approvals and maintain regulatory compliance across our product portfolio.

 

As the Director of Regulatory Affairs, your responsibilities will include:

Regulatory Strategy

Develop and implement the U.S. regulatory strategy aligned with the company’s business goals and objectives

Lead and execute U.S. regulatory activities, ensuring compliance for product marketing

Serve as key regulatory team leader for business development activities (due diligence)

Provide regulatory expertise and guidance to senior management and cross-functional teams.

Lead the preparation and submission of regulatory filings (e.g., 510(k), PMA, NDA, BLA) for new products, product modifications, and renewals

Advise on regulatory risks and offer strategies for risk mitigation throughout the product development lifecycle

 

Regulatory Advertising, Promotion and Labelling:

Serve as the company subject matter expert for regulatory review of advertising and promotion materials and provide regulatory leadership to the respective cross-functional teams, providing direction and regulatory expertise for promotional materials

Contributes to promotional review committee for all company products and medical device

Responsible for regulatory product/promotional review for drug and medical device products

Provides regulatory review for labelling submissions.

Ensures regulatory requirements are met for promotional materials submissions and labeling submissions (annotations, Structured Product Labeling (SPL) documents).

Leads process to update PI or labeling components including managing meetings, timelines, and review process.

Ensures labeling is consistent with core company position.

 

Compliance:

Assures product compliance with applicable regulations throughout the lifecycle of the product

Identifies and communicates the impact of new regulations on company products.

Develops and maintains current regulatory knowledge in the areas of advertising and promotion and CCDS and advises management of significant developments

Maintains regulatory and technical sections of CTD filings to ensure compliance with global filings in line with company scientific data