Team: R&D, Pharmacovigilance & RegulatoryAffairs
Job Type: Direct Employee
Contract Type: Permanent
Location: Parma, IT
About us
Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over...
work in a multicultural and dynamic environment. We are looking for a Legal Confidentiality Assessment Assistant to work in the Legal Affairs Unit. EFSA is committed to supporting the careers of people with visible and invisible disabilities that are...
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Team: R&D, Pharmacovigilance & RegulatoryAffairs
Job Type: Direct Employee
Contract Type: Permanent
Location: Parma, IT
About us
Based in Parma, Italy, Chiesi is an international research...
manufacturing plants (internal and external) and Global RegulatoryAffairs.
Experience Required
At least 4-5 years of experience in Regulatory or Quality Assurance positions in the pharmaceutical industry.
Education
Degree in scientific disciplines (CTF...
Team: R&D, Pharmacovigilance & RegulatoryAffairs
Job Type: Direct Employee
Contract Type: Permanent
Location: Parma, IT
About us
Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over...
Select how often (in days) to receive an alert:
Team: R&D, Pharmacovigilance & RegulatoryAffairs
Job Type: Direct Employee
Contract Type: Permanent
Location:
Parma, IT
About us
Based in Parma, Italy, Chiesi is an international research...
Select how often (in days) to receive an alert:
R&D Scientific Information Specialist - Temporary
Date: 2 Jan 2025
Department: Strategy, Sustainability & Growth
Team: R&D, Pharmacovigilance & RegulatoryAffairs
Job Type: Direct Employee...
administrative tasks within the RegulatoryAffairs, Finance, Operations, and HR departments, as applicable.
• Manage the Cavriago reception desk, telephone/fax, internal distribution of mail & faxes, visitors’ reception, and registration.
• Organize general...
pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatoryaffairs, pharmacovigilance, intellectual property, quality assurance, R&D project and portfolio...