Experteer Overview In this role you will author, review, and manage regulatory documents that translate clinical, nonclinical, and CMC data into compliant submissions for global authorities. You will serve on cross‑functional teams to ensure scientific rigor and
API Industrial Manufacturing & LCM Sr Director Date: 2 Jul 2026 Business Area: Industrial Operations & HSE Job Type: Direct Employee Contract Type: Permanent Location: Parma, Italy. The role offers flexibility, combining on‑site presence with remote
This is what you will do An experienced Clinical Operations Lead with a strong background in global drug development, capable of providing strategic and operational leadership across complex clinical development programs. The Clinical Operations Lead (COL)
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose:
Experteer Overview In this role you will support Chiesi’s Global Rare Diseases portfolio by managing CMC regulatory activities across submissions and lifecycle. You will collaborate with Core teams, GCST, and external CMOs to ensure compliance and
R&D GRAPS Affiliate and Partnership Oversight Unit Head Location: Parma, IT Responsibilities Assure that relationships with Partners and Affiliates are duly managed in the light of patient safety related matters and regulations both at global and
Experteer Overview You will support Global Technical Operations & Supply by governing training and documentation systems. You’ll implement the new electronic document management project and ensure compliance with regulatory standards. The role sits at the crossroads
Experteer Overview In this role you will oversee external manufacturing partners to ensure reliable product availability for global markets while balancing service, inventory, and cost. You will lead a cross-functional team and act as the main interface
Experteer Overview In this role you will coordinate SDEA and related contracts to ensure patient safety and global regulatory compliance. You will partner with business development, alliance management and legal teams to identify contracts needing SDEA
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT (role can be based in one of
Experteer Overview In this role you will develop regulatory strategies for EU and international markets for Chiesi Global Rare Diseases. You will coordinate regulatory submissions and provide guidance on regional requirements to support product development and
Business Area R&D, Pharmacovigilance & Regulatory Affairs Job Type Direct Employee Contract Type Permanent Location Italy, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries,
Overview Experteer OverviewIn this role you will support GRAPS to ensure the pharmacovigilance system aligns with regulatory expectations. Based at the Parma headquarters with hybrid work, you will help maintain PSMF readiness, monitor PV KPIs, and