Metered-Dose Inhalers (MDIs), supplies Group’s Affiliates and distributes directly to clients at a local level and in export markets.Who we are looking forPurposeThe Corporate Regulatory Compliance Senior Specialist will report to the Head of Global...
and accurate country internal and external reporting.
Main accountabilities of the role:
1. Maintain transaction processes and systems to ensure effective financial reporting and operational information;
2. Prepare journal entries, recurring and allocation...
regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D project and portfolio management. Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important...
cybersecurity and compliance, and enjoys constantly learning and sharing.
Your Key Responsibilities:
Reporting to the CRIF Cybersecurity Manager you will be responsible for the following:
• Assist in Vendor and Third-Party Cybersecurity Management through...
regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D project and portfolio management. Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important...
and regulatoryreporting
• Lean Finance: Improve efficiency through standardization, automation in the Finance function. Establish and improve manual and system internal controls, including segregation of duties, to ensure an effective and efficient internal...
Manager;
• participate in the periodical internal meeting and third parties meeting (client, local authority, etc..) issuing the necessary documents;
• issue the monthly HSE reports and final project report;
• evaluate the success of overall project HSE...
Head of Global Pharmacovigilance Center of Excellence
Date: 13 Feb 2025
Team: R&D, Pharmacovigilance & Regulatory Affairs
Job Type: Direct Employee
Contract Type: Permanent
Location: Parma, IT
About us
Based in Parma, Italy, Chiesi is an...
investigational product, questionnaires, etc.
• Trial status and trial team tracking and reporting
• Update of clinical trial registries
• May participate in co-monitoring visits to study sites
• Review of Monitoring Visit Reports
• May assist in review of study...
About the Role:
We are looking for a highly skilled Manufacturing Engineering Manager to play a key role in optimizing our manufacturing processes and driving continuous improvement initiatives. Reporting to the Plant Manager, you will lead the...
and explaining the interpretation of law or legal positions at internal meetings, Support the Transparency and Confidentiality Team Leader acting as central contact point at EFSA towards internal and external stakeholders for transversal reporting matters...
regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D project and portfolio management. Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important...
Maintain VAT registers, reconcile tax accounts, and ensure timely tax payments. Assist in audits and monitor regulatory changes.
2. Tax Compliance: Maintain tax calendar, manage tax obligations and respond to public authority requests, and handle claims...
and international regulatory safety reporting requirementsKnowledge of MedDRA coding dictionary and its principles Ability in managing performance and projectsUp-to-date knowledge of local/ global post-market regulations (e.g. Good Pharmacovigilance PracticesIT...
background in Pharmacovigilance will be considered as a plus.
Technical Skills
• Knowledge of national and international regulatory safety reporting requirements (post-marketing and clinical trials)
• Knowledge of MedDRA coding dictionary and its principles...
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