• Senior Manager, Regional Regulatory Affairs State Line
  • CSL in State Line, PA, United States
  • jobs
  • 1 week ago

jobs description

CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives.

With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies... to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions.

Could you be our next Senior Manager of Regional Regulatory Affairs? This position is located in our King of Prussia PA office. It is a Hybrid role. You will report to the Director, Regional Regulatory TA Lead.

• You will be the primary CSL representative to regional health authorities for assigned products.
• Develop the establishment and maintenance of high quality relationships with regional health authorities and collaborating with respective GRA Global Regulatory Leads (GRLs) (Global Product Strategy or CMC) and team members to enhance these relationships.
• Contribute to regulatory and account for changes in relevant regulations / laws helping CSL’s business within the Region North America and providing regulatory assessment of these changes.
• Assure a productive collaboration with important company partners, such as Regional commercial operations, to ensure successful development, strategic agreement and execution of regional regulatory strategies that result in successful applications for assigned products, from early development to Marketing Authorization (MA), and for any post MA submissions.
• You will contribute regional regulatory perspective to the global regulatory strategy and aligning regional strategies with the global strategy throughout the product lifecycle for assigned products.
• Guide. facilitate comprehensive, commercially and globally aligned regulatory activities within GRA NA for assigned products throughout development and after commercialization.
• Be a GRA NA representative for assigned projects to the Global Regulatory Affairs Strategy Team (GRAST) to provide regional input into the delivery of science-based and globally aligned regulatory strategy with GRL.

Your Experience
• A bachelor’s degree in Science or Pharmacy.
• 7+ years of experience in the pharmaceutical industry in Biologics/Research & Development, some experience may be accounted for with advanced degree.
• 3+ years of experience in regulatory, supported by additional pharmaceutical /industry experience. Direct regulatory-facing experience
• Working knowledge of regulatory guidelines and legislative requirements for US FDA regulations.
• Experience in negotiations and facilitating resolution of issues with regulatory agencies and with positive outcomes.
• Driving complex projects throughout a product’s lifecycle utilizing broad experience with health authorities or project teams

• Medical, Dental, Vision
• 401k

State Line PA USA


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