Global Regulatory Affairs Specialist

Social network you want to login/join with: Global Regulatory Affairs Specialist, Modena This job posting is for a Global Regulatory Affairs Specialist position at Chiesi Farmaceutici , a top 50 pharmaceutical company with over 80 years of experience in the pharmaceutical and biotechnology industry. The role is based in Modena and requires an EU work permit. Job Details Client: Chiesi Farmaceutici Location: Modena Job Category: Other Job Reference: 8160257735766573056337112 Job Views: 1 Posted: 08.05.2025 Expiry Date: 22.06.2025 Job Description Our client, Chiesi Farmaceutici , is seeking a Global Regulatory Affairs Specialist to join their dynamic and international team. The role involves contributing to global regulatory strategies, ensuring alignment with product labelling, and managing interactions with health authorities. Responsibilities Serve as a regional/local regulatory lead and contact for health authorities. Develop and execute health authority engagement strategies. Lead regulatory submissions and ensure timely delivery. Prepare and review regulated documents. Support inspections and compliance activities. Provide updates on project statuses. Requirements Approximately 3 years of experience in Regulatory Affairs. Understanding of clinical development and LCM activities. Experience with electronic document management systems, e.g., Veeva Vault. Strong organizational and strategic skills. Skills Emerging understanding of drug development. Ability to handle multiple projects. Multicultural sensitivity. Soft Skills Stress and time management. Planning and organizational skills. Strategic thinking. What We Offer Competitive salary. Permanent contract. Chemical contract. Applicants must meet the specified requirements. Please provide consent for data processing as per GDPR. This opportunity is open to candidates of all genders. J-18808-Ljbffr

Location: provincia-di-modena, IT

Posted Date: 6/17/2025