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Hjem - Node - (Senior) Global Regulatory Affairs Managers, CMC

(Senior) Global Regulatory Affairs Managers, CMC

(Senior) Global Regulatory Affairs Managers, CMC
Engelsk

Driven by research and a passion for science, Ferring Pharmaceuticals is a biopharmaceutical company dedicated to the development of innovative treatments that make a real difference in people’s lives all over the world. Active in the areas of reproductive medicines & womens health, urology & uro-oncology and gastroenterology & liver diseases, we develop medicine on the body's own terms. We believe in the power of people and research - and go where ideas and research take us. 

We are seeking new colleagues with various degrees of seniority to a newly established Global Regulatory Affairs CMC department at Ferring. Joining the team now, you will be able to influence the future way of working in the department and you will be part of achieving our goal - building a department to be characterized by Regulatory Affairs CMC excellence. 

THE DEPARTMENT 

The Global Regulatory Affairs CMC department consists of 30 regulatory product/project managers and regulatory product leads split in four teams with three teams based in Copenhagen and one team based in Israel. The vacant positions are all in the Copenhagen teams. The department is responsible for all global regulatory CMC activities during development, registration and approval as well as for worldwide market expansions and CMC lifecycle activities. The department has a robust expertise with small molecules, peptides, biologics and recombinant products and are now expanding to also excel in other modalities.   

THE JOB 

Reporting to an Associate Director, Global Regulatory Affairs, CMC, your main responsibilities will be as listed below. You will be supporting or driving activities, depending on your level of experience: 

  • Formulate, lead and drive the global regulatory CMC strategy for development projects and marketed products with a focus on creativity and innovation, maximizing the business benefit balanced with regulatory compliance 
  • Lead all global CMC submission activities for assigned projects/products, while applying the global strategy into submissions  
  • Responsible for regulatory submissions and approvals for worldwide market expansions and renewals 
  • Provide regulatory CMC expertise to cross-functional teams such as the Global Regulatory Project Teams, CMC Teams, Product Teams and Launch Teams  
  • Perform regulatory impact assessment of CMC changes for established products and development projects, ensure that adequate documentation is generated to support the change and ensure that the variation is approved by regulators  
  • Plan and participate in Health Authority meetings in relation to CMC activities. In close collaboration with subject matter experts you will be responsible for setting objectives, preparing briefing books, coordinating and planning rehearsals and risk mitigation plans in relation to meetings with Health Authorities 

You will be working in an international environment and have interfaces with many different disciplines including other Regulatory disciplines, Global Pharmaceutical R&D, Product Supply, Ferring’s affiliates and development sites around the world. 

YOUR QUALIFICATIONS 

The ideal candidate holds a degree in life science or Pharmacy, with at least 3 years of experience in global regulatory affairs for a Global Regulatory Affairs Manager position and at least 7 years of experience for a Senior position. Preferably the working experience includes regulatory CMC activities and preferably with a variety of modalities. 

You have excellent administrative skills and are good at communicating verbally and in writing.  

You must have a proactive mindset and a desire to continuously develop and find innovative solutions to regulatory challenges. In addition, you are well-organized and have the ability to plan, execute and meet deadlines. You have good negotiation skills and can deal with ambiguity. You are a true team player, an experienced user of IT (including MS Office), and are keen on working in a multicultural corporate environment. 

ADDITIONAL INFORMATION 

Further information about the positions can be obtained by contacting any of the Associate Directors below heading up our different teams: 

Associate Director, Lena Høvring Von Grumbckow, Global Regulatory Affairs, CMC, Gastroenterology & Liver Diseases. Mobile: +45 28787561 

Associate Director, Pernille Maria Manuel, Global Regulatory Affairs, CMC, Reproductive Medicine & Women Health. Mobile: +45 28787170 

Associate Director, Katrine Rasmussen, Global Regulatory Affairs, CMC, Urology & Uro-oncology. Mobile: +45 28787674 

 

Your application and CV in English should be sent as soon as possible but no later than 10th of June 2018, as we will be reviewing incoming applications on an on-going basis. 

Apply

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