16 ott - Siena
We make it
We make it GmbH is a company operating nationally in Switzerland. Thanks to many years of successful experience, it has a high level of competence in the personnel services sector. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the highest demands on quality, ethics and discretion.
For our customer, the company CSL Seqirus, are we searching for:
Global Regulatory Affairs Associate
Description
CSL Seqirus is one of the world’s largest influenza vaccine companies, specializing in the development and manufacture of vaccines to help prevent influenza. The company uses both egg-based and cell-based technologies and has extensive research and production expertise. Its manufacturing facilities are located in the United States, the United Kingdom and Australia. CSL Seqirus is also a global leader in influenza prevention and a key partner in pandemic preparedness. Every year, its influenza vaccines help protect millions of people from seasonal influenza.
Work hours
Standard 41h / Week
Duration
6 Months
Tasks
Lead and execute regulatory strategies for assigned products and projects, Prepare, compile, and submit highquality regulatory applications, including variations, renewals, and responses to health authority questions, Ensure regulatory dossiers remain compliant and up to date for EU, UK, and Switzerland markets, Provide regional regulatory expertise to support global development, CMC, compliance, and labeling activities, Liaise with regulatory authorities and support regulatory agency interactions, Collaborate with cross-functional stakeholders including Regulatory Affairs, Quality, Medical, Pharmacovigilance, Commercial Operations, and Business Development teams
Qualifications
Degree in Biological Sciences, Pharmacy, Allied Medical Discipline, or related field (advanced degree preferred), Minimum 5+ years of Regulatory Affairs experience within the
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