Denmark Job Openings
Ferring Pharmaceuticals, Inc.
Global Regulatory Affairs Manager - CMC (18 months Fixed term position)
Kastrup
FULL TIME
October 4, 2024
Would you like to join an international company with excellent development opportunities and an open work environment where your contributions will make a difference, as you take on CMC responsibility for one of our products and a development projects?
Would you like to join us in a challenging position in our regulatory CMC department? We are looking for a new colleague to our team who will be responsible for one of our well-stablished products supporting the lifecycle projects.
The positions will be placed in Ferring’s spectacular brand-new facility located close to Copenhagen airport. Here you will be surrounded by highly skilled and equally dedicated colleagues including various experts and specialists that you will collaborate with as part of your project execution.
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Responsible for the CMC part of regulatory submissions and approvals for worldwide market expansions and approvals
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Provide regulatory CMC strategy and expertise to cross-functional teams such as the Global Regulatory Project Teams, CMC Teams, Product Teams and Launch Teams
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Perform regulatory impact assessment of CMC changes for the development projects and established product and drug substance, ensure that adequate documentation is generated, submitted and approved timely worldwide.
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Drive and execute Scientific Advice with national Competent Authorities in relation to CMC activities.
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Participate actively in development and optimization of departmental and working processes.
Behind our innovation – There’s you
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Experience in global regulatory affairs preferably within regulatory CMC activities.
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M.Sc. in a life science or pharmacy.
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Facilitation of risk management discussions is an asset.
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A desire to find innovative solutions to regulatory challenges and a proactive mindset.
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Well-organized and can plan, execute and meet deadlines.
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True team player.
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Good negotiation skills and the ability to deal with ambiguity.
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Experienced use of IT (including MS Office).
The Global Regulatory Affairs CMC department consists of approximately 30 global regulatory product/project managers, regulatory product leads, and medical device managers split in three teams all based in Copenhagen. You will be part of the Small Molecule team who are responsible for the small molecules and peptides products. 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 for products and medical devices. The CMC department has a robust expertise with small molecules, peptides, biologics, recombinant products and are expanding to also excel in other modalities incl. gene therapy.
Behind our Purpose... There’s you
If you have questions about the recruitment process, please contact Senior Talent Acquisition Sourcer, Patricia Martins <Patricia.Martins@ferring.com>
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 on scientific advances 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.
Note to agencies: this search is being managed by Ferring’s Talent Acquisition team. Kindly do not send us spontaneous profiles.
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