Global Regulatory Submission Manager

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Kastrup, Syddjurs, Midtjylland, DNK
In-Office
Software • Biotech • Pharmaceutical
The Role
Job Description:

Do you have experience with Global Regulatory Submissions?
In this position as Global Submission Manager, you will play an active role throughout the entire submission lifecycle—from planning regulatory activities to final publishing.

Our International Pharma Science Center (IPC) in Denmark – Part of Ferring Pharmaceuticals
Ferring Pharmaceuticals is a global biopharmaceutical leader in reproductive medicine, maternal health, and key areas within gastroenterology and urology.
By joining our International Pharma Science Center (IPC) in Kastrup, you become part of Ferring’s global network—collaborating across functions in a state-of-the-art waterfront building with stunning views of Sweden and easy access to Copenhagen Airport. You’ll work on-site with 600 highly skilled colleagues in an international, dynamic, and collaborative environment.
 

Ferring +You – Our collaboration
You will join a small, dedicated Global Submission Management team of experienced colleagues. The team serves as a central function in Ferring, responsible for electronic regulatory submissions across the EU, CA, AU, EAEU and several other regions. We collaborate closely with Regulatory Affairs globally and work in a fast-paced environment where continuous improvement and cross‑-functional‑ partnership are key. The team reports to the Associate Director, Head of Global Submission Management.

Your day at Ferring- Tasks where you are accountable
As a Global Submission Manager, you will coordinate and execute global regulatory submissions across multiple regions and time zones. You will be involved in the full submission lifecycle—from planning regulatory activities to dossier publishing—requiring a solid understanding of end-to-end processes.
 

Your key responsibilities include:

  • Managing preparation, submission, publishing, and lifecycle management of eCTD and other regulatory formats dossiers.

  • Maintaining regulatory documentation and global applications, including variations and work-sharing procedures.

  • Collaborating closely with cross-functional teams to ensure high-quality and timely submissions.

  • Providing guidance on eCTD/non‑eCTD requirements and contributing to continuous optimization of submission processes.

  • Prioritizing and coordinating multiple projects, proactively addressing submission-related challenges.

  • Training global colleagues in regulatory processes, systems, and tools.

Behind our entrepreneurship … there´s your skills

To succeed in this position, you need technical flair and IT systems understanding, as well as the ability to bring structure and clarity to everything you do – also when you have tight deadlines.
 

We imagine you have:

  • Hands-on experience with a publishing system preferrable Lorenz and a document management system preferable Veeva.

  • Knowledge of eCTD requirements and electronic submission processes (highly desirable).

  • Proven experience in Regulatory Affairs with a solid understanding of end-to-end regulatory filing processes.

  • Excellent written and verbal communication skills, with the ability to convey complex information clearly to diverse stakeholders.

  • A relevant master’s degree, or relevant work experience

Become a part of Ferring – apply now
If our mission and your vision are aligned, apply via the link in the job ad and include a short motivation in your CV.
Please note that applications are reviewed continuously, and we close the process when we find the right match.
We are unable to offer relocation assistance for this position.
Candidates must be located in the Øresund region.

Note to agencies:
This search is being managed by Ferring’s Talent Acquisition team. Kindly do not send us unsolicited profiles.

About Ferring Pharmaceuticals.
At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused in the areas of reproductive and women’s health, gastroenterology, and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world. Read more at ferring.com.

Location:Ferring Denmark

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The Company
HQ: St-Prex
5,940 Employees
Year Founded: 1950

What We Do

Ferring Pharmaceuticals is a privately owned, research-driven, specialty biopharmaceutical group committed to building families and helping people live better lives. We are leaders in reproductive medicine and maternal health, and in areas of gastroenterology and urology. We are at the forefront of innovation in microbiome-based therapeutics and uro-oncology intravesical gene therapy. Ferring was founded in 1950 and employs more than 7,000 people worldwide. The company is headquartered in Saint-Prex, Switzerland, and has operating subsidiaries in more than 50 countries which markets its medicines in over 100 countries. Community guidelines available here: https://re.ferring.com/Ferring-LinkedIn-Community-Guidelines Social Media Privacy Notice available here: https://www.ferring.com/social-media-privacy-notice/

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