Associate Global Labelling Manager
Job Description
Job Description:
Would you like to join us in a challenging position as Associate Global Labelling Manager in the Global Regulatory Compliance Excellence department at Ferring? We offer an exciting job in an international company with great opportunities to learn and make an impact.
Ferring +You – Our collaboration
The Global Regulatory Compliance Excellence team enables GRA to deliver compliant, high‑quality and strategically aligned outcomes by transforming regulatory intelligence into actionable insights, strengthening quality systems and processes, and driving performance through collaboration and continuous improvement. The team consists of 6 full-time employees and 4 students, reporting to the Head of Global Regulatory Compliance Excellence.
Your day at Ferring- Tasks where you are accountable
As Associate Global Labelling Manager, you will coordinate and execute global regulatory labelling and compliance activities across multiple regions and time zones.
Your main responsibilities will be as follows:
- Contribute to the regulatory expertise in global labelling processes, providing labelling advice, training, and coordinating global labelling changes and activities, including review and quality control of labelling documents;
- Compliance responsibilities include adhering to SOPs and training requirements, authoring and reviewing related documents, managing safety variation monitoring;
- Maintaining oversight of Company Core Data Sheets (CCDS);
- Provide input to Pharmacovigilance System Master File(PSMF) Annexes F and H to support PSMF updates related to Periodic Safety Update Report (PSUR) Submission, Safety Variation and Risk Minimisation Measure compliance;
- Supporting regulatory Labelling, Non-Clinical & Clinical documentation for all market expansions, including the EU SmPC/PIL for CP, MRP/DCP as well as the English common mock-ups and artworks;
- Conduct linguistic review of Central Procedure (CP) documentation to ensure compliance with EU language requirements, coordinate translation of labelling documents and ensure readability testing of labelling documents are included in the submission in due time, when required;
- Document handling in the regulatory electronic document management system and overview of data in the regulatory information management system.
Behind our entrepreneurship … there’s you
The ideal candidate holds a degree in Life Science or Pharmacy and has some previous experience with managing global regulatory activities - preferably within labelling, and other clinical and non-clinical regulatory activities.
You must have a proactive, collaborative, detailed-oriented mind-set combined with the ability to plan and execute regulatory objectives in a timely manner. You have good judgment and decision-making skills. You are a true team player with a positive mindset and a constructive attitude to drive results, and you are keen on working in an international corporate environment.
Fluency in English, both spoken and in writing, is required.
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.
If you have any questions, you are welcome to contact Ruth Greisiger, Associate Director at +45 2878 7210.
We are unable to offer relocation assistance for this position. Candidates must be located in the Øresund region.
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.