RA Principal Associate
1 giorno fa
Sassari, Sardegna, Italia
K-Recruiting GmbH
Tempo pieno
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RA Principal Associate (M/F/X) Tasks:
* Lead and execute regulatory strategies for assigned products and projects.
* Prepare, compile, and submit high-quality 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. Qualification:
* Degree in Biological Sciences, Pharmacy, Allied Medical Discipline, or related field (advanced degree preferred).
* Minimum 5+ years of Regulatory Affairs experience within the pharmaceutical or biotechnology industry.
* Strong experience with regulatory submissions and registrations in the EU, UK, and Switzerland.
* Experience managing regulatory applications, variations, renewals, and health authority interactions.
* Exposure to Veeva and regulatory application management systems is highly desirable.
* Experience in vaccines and/or biologics is advantageous.
* Strong project management, stakeholder management, and communication skills.
* English proficiency is required as all Seqirus business is conducted in English
Requirements:
Start: Within the next four weeks Duration: 6 months Capacity: 5 days per week
Location:
Tuscany (IT) #J-18808-Ljbffr
* Lead and execute regulatory strategies for assigned products and projects.
* Prepare, compile, and submit high-quality 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. Qualification:
* Degree in Biological Sciences, Pharmacy, Allied Medical Discipline, or related field (advanced degree preferred).
* Minimum 5+ years of Regulatory Affairs experience within the pharmaceutical or biotechnology industry.
* Strong experience with regulatory submissions and registrations in the EU, UK, and Switzerland.
* Experience managing regulatory applications, variations, renewals, and health authority interactions.
* Exposure to Veeva and regulatory application management systems is highly desirable.
* Experience in vaccines and/or biologics is advantageous.
* Strong project management, stakeholder management, and communication skills.
* English proficiency is required as all Seqirus business is conducted in English
Requirements:
Start: Within the next four weeks Duration: 6 months Capacity: 5 days per week
Location:
Tuscany (IT) #J-18808-Ljbffr