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
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
Data Management Specialist Overview The Data Management Specialist will join Global Clinical Science department of Menarini Stemline, the R&D organisation of the Menarini Group. As a Data Management Specialist, you will develop and maintain the eCRF and other data collection
About Camlin Group: Camlin is a global technology leader with a bold vision: to bring revolutionary products to life across diverse industries like power and rail. Our passion extends to pioneering R&D projects in various scientific
Select how often (in days) to receive an alert: QA Validation & Equipment Compliance Manager Date: May 30, 2026 Department: Quality Operations Italy, Parma Site Job Type: Direct Employee Business Area: Quality Contract Type: Permanent Location: Parma,
This is what you will do We are seeking a skilled Process Engineer to oversee and optimize pharmaceutical manufacturing processes. This role is responsible for ensuring process efficiency, robustness, and compliance with GMP and regulatory standards,
Teoresi S.p.A. - 35+ years of history, 8 companies across Italy, the United States, Germany, and Switzerland, 1200+ professionals, 4 acquisitions in a single year, 1 partner, and one comprehensive solution. We are always looking for
Who we are looking for The R&D Bioinformatician Lead drives and executes hands‑on bioinformatics analyses in support of target identification and translational research across programs. The role includes full methodological ownership, with responsibility for shaping and
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:
Disclaimer: To be eligible, you’ll need to be based in the UK, France, Germany, Italy, or Luxembourg. The role will also involve regular travel across our sites in EMEA. Who We Are: At CloudHQ, our mission
This is what you will do The R&D Bioinformatician Lead drives and executes hands-on bioinformatics analyses in support of target identification and translational research across programs. The role includes full methodological ownership, with responsibility for shaping
Company Description NowVision is redefining construction payments through its AI-native validation platform, ensuring progress payments are released based on verified, completed work. By eliminating ambiguity, reducing disputes, and protecting capital, the company streamlines collaboration across owners, EPMs,
Select how often (in days) to receive an alert: Business Area: Industrial Operations & HSE Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90
Omnichannel Engagement & Marketing Automation Platforms Manager - Fixed term contract About Barilla At Barilla, we believe that every great journey begins with passion and a bold vision. From our humble beginnings in 1877 in a
Chiesi Research & Development Our R&D team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology,
Toyota Material Handling Europe is expanding its R&D team and is looking for a Normative Requirements & Regulatory Compliance Engineer. In this role, you will ensure the normative, regulatory, and documentation compliance of products and machines
Corporate Quality Auditing Senior Specialist Date: 10 Apr 2026 Department: Corporate Quality Operations Business Area: Quality Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT This is what you will do Carrying out GMP/ISO audits
Experteer OverviewIn this role you will optimize pharmaceutical manufacturing processes to ensure efficiency, robustness and GMP/regulatory compliance. You will support production, technology transfer and continuous improvement within Global TechOps & Supply. You will analyze process data, drive
Experteer OverviewIn this role you drive hands‑on bioinformatics analyses to support target identification and translational research. You will own methodological strategy, shape pipelines, and ensure rigor across data‑driven outputs. You’ll collaborate with translational leads and cross‑functional teams