Director, CMC Regulatory Affairs

Antwerp - Belgium

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

People Leader

All Job Posting Locations:

Beerse Antwerp Belgium Warsaw Masovian Poland

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at are searching for the best talent for Director CMC Regulatory Affairs. This hybrid work position will be located in Beerse Belgium Warsaw Poland Allschwil Switzerland or our East Coast USA location (Horsham PA Spring House PA Titusville NJ and Raritan NJ)

Director CMC Regulatory Affairs Synthetics New Modalities

As Director CMC Regulatory Affairs Synthetics New Modalities you will lead a team of experts and develop implement and maintain the global CMC strategy for our most innovative synthetic product this role you will combine in-depth technical expertise with strategic insight to navigate complex regulatory landscapes and drive innovation within Johnson & Johnson.

What you will do:

Leadership:Coach and inspire a high-performing team of CMC professionals fostering a culture of continuous improvement and scientific excellence.
Execution:Translate complex objectives into measurable results and projects.
Collaboration:Act as the bridge between CMC RA and senior leadership to ensure an agile and competitive organization. Represents CMC RA on cross-functional teams
Compliance & Ethics:Ensure the highest regulatory standards while promoting a culture of innovation.

Qualifications & Skills

Education:BS in Biological Pharmaceutical Chemical Sciences or Engineering.MS Ph.D. or Pharm.D. preferred.
Experience:12 years of experience within the pharmaceutical/healthcare industry with a focus on CMC Regulatory Affairs.
Expertise:Deep knowledge of global regulatory laws guidance and submission routes (ICH FDA EMA).
Technical Understanding:Strong background in chemistry biology or engineering relevant to product development.
Leadership & Communication:Proven ability to communicate effectively and to lead cross-functional teams.
Strategic Mindset:Ability to identify priorities drive results and act as a model of leadership.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to follow local requirements. While you are welcome to apply to any or all of the postings we recommend focusing on the specific country(s) that align with your preferred location(s).

United States - Requisition Number: R-060742
Switzerland - Requisition Number: R-060740

Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.

Required Skills:

Preferred Skills:

Required Experience:

Director