Chiesi Farmaceutici S.p.A. is seeking a Subject Matter Expert for Process Validation in Parma, Italy. In this role, you will support industrialization and lifecycle management for various pharmaceutical products. The successful candidate will need a Bachelors degree in
This is what you will do You will act as Subject Matter Expert for Process Validation and technical maintenance activities, supporting industrialization, product technology transfer and life cycle management for Respiratory, Orals & Small Molecules products. You will
Chiesi Farmaceutici S.p.A. is seeking a Subject Matter Expert for Process Validation and technical maintenance activities in Parma, Italy. Youll support industrialization and technology transfer for respiratory, oral, and small molecule products, ensuring compliant manufacturing processes. The ideal
Experteer Overview In this role you act as the global technical reference for Respiratory, Orals & Small Molecules, ensuring robust, compliant manufacturing tech throughout the product lifecycle. You’ll contribute to industrialization strategies within R&D Product Teams
Application close date:Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We’re working to
Application close date:Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We’re working to
Application close date:Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We’re working to
JOIN THE TEAM THAT’S POWERING PROGRESS Building cities. Driving commerce. Fueling Progress. For over 100 years, Allison has powered the vehicles and technology that move our world forward. What powers us? Our employees. From the first
JOIN THE TEAM THAT’S POWERING PROGRESS Building cities. Driving commerce. Fueling Progress. For over 100 years, Allison has powered the vehicles and technology that move our world forward. What powers us? Our employees. From the first
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,
Head of Biologic Drug Substance - Process & Analytical Development Date: 30 Apr 2026 Department: GTD Global Technical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About
Questa posizione è in Chiesi Group Riassunto dellopportunità da parte della Joinrs AI : Chiesi Group cerca un QA Validation & Equipment Compliance Manager con laurea in discipline scientifiche o ingegneristiche. Il ruolo prevede la supervisione delle
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, while supporting
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, while supporting
Experteer Overview As Head of Biologic Drug Substance Process and Analytical Development, you will define and drive the CMC strategy for biologics from research to launch. You will lead the Drug Substance process and analytical development, ensuring compliance,
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
Experteer Overview In 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,
# Senior Process EngineerCollecchio, ItalyApply NowFind out how well you match with this jobJob ID81156Senior Process Engineer Collecchio (PR), Italy Nestled in the picturesque surroundings of Collecchio, near the vibrant city of Parma, dsm-firmenich is proud to announce
Experteer Italy is searching for an experienced professional to optimize pharmaceutical manufacturing processes in Parma. The role requires thorough knowledge of GMP compliance and process validation, alongside 8+ years in pharmaceutical manufacturing or engineering. You will work on
Come join us and shape the technological future of Digital Payments ! You’ll be part of an international agile team that delivers state-of-the-art Digital Solutions to facilitate and enhance payment experience . Data & Analytics represent