Chiesi Farmaceutici S.p.A. is seeking a qualified lawyer to join its Global Legal, Compliance & IP team in Parma. The role provides legal support across staff functions with global responsibilities and Global R&D, including drafting and negotiating
Full time on site position offers great opportunities for career growth. Date: 13 Jul 2026 Department: Global Legal, Compliance & IP Business Area: Legal, Compliance & Internal Audit Job Type: Direct Employee Contract Type: Permanent Location:
Apply for Legal Counsel - Temporary Contract at Bormioli Pharma in Parma, EMI, IT. This Full time on site position offers great opportunities for career growth. The resource will be responsible for managing all the following
About Us ProductLife Group (PLG) is a dedicated life sciences and pharmaceutical outsourcing and consulting company providing expertise and services in areas such as Product Development, Market & Patient Access, Regulatory Affairs and Safety & Vigilance
Free day to volunteer Your responsibilities and tasks Design and configure homogenizers according to customer specifications and project requirements. Provide technical support and expertise to internal departments throughout the project lifecycle. Collaborate with the Sales team
About us 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
About us 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
Specific activities and responsibilities: - Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment - Preparation of validation protocols, reports and related documentation. - knowledge of GMP regulations - Ensure compliance
Specific activities and responsibilities: - Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment - Preparation of validation protocols, reports and related documentation. - knowledge of GMP regulations - Ensure compliance