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Global Regulatory Affairs Associate

Pubblicato il 16-10-2026 - We make it in Siena

Global Regulatory Affairs Associate 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: 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

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