Key Responsibilities - Executes analyses on excipients, raw materials, finished products, and packaging per internal SOPs and applicable pharmacopeias. - Conducts stability studies, process and method validations, and activities related to tech transfer of pharmaceutical products. - Performs instrument qualification and re-qualification (IQ/OQ/PQ) according to internal procedures. - Records...
Job description Join our team as Process Validation Consultant and start a new adventure in an international and dynamic environment where you will be able to fulfil your career expectations in a fast-growing organization.Being a consultant at Amaris Consulting means positioning yourself as a technical and functional expert in an industrial field but above all being an ambassador of our...
Who are we? Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different...
Summary Plan, perform and report scientific experiments with SME (subject matter expert) to support the innovation projects and/or advance the innovation technical platform of radiopharmaceutical parenteral dosage forms. Contribute to maintenance of laboratory instruments/infrastructure. About The Role Key responsibilities - Plan and execute characterization studies, analytical tests, and...
Summary The Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. About the Role Major accountabilities : - Support site validation planning by writing and...
A global healthcare company seeks a Regional Planning & Logistics Supervisor in Ivrea, Italy, to develop distribution plans for radiopharmaceuticals. This role involves managing supplier activities, ensuring compliance with GxP regulations, and collaborating with various stakeholders to maintain a continuous supply chain. The ideal candidate will have a degree in Science or Engineering, solid...
A global pharmaceutical company in Ivrea is seeking a Chemistry Laboratory professional. The role includes executing analyses on excipients, raw materials, and finished products while adhering to internal SOPs. Candidates must possess a Chemistry degree, solid knowledge of pharmaceutical quality control, and experience in a GMP environment. Fluency in Italian and English is required. Join us in...
RLT Systems Integration Governance Manager Join to apply for the RLT Systems Integration Governance Manager role at Novartis Italia This role is responsible for architecting the structure and governance of data across key domains of the RLT (Radio Ligand Therapy) Supply Chain, including Integrated Business Planning (IBP), Planning, Logistics, Product Lifecycle Management (PLM) and Artwork. It...
Regional Planning & Logistics Supervisor – EMEA Overview The Regional Planning & Logistics Supervisor – EMEA is responsible for generating optimal distribution plans for radiopharmaceutical (RLT) products across the EMEA Region. The role balances risk and cost while managing supplier activities, CAPA investigations, supplier risk assessments, qualifications, validations, and logistics projects...
A consultancy firm in Piemonte is seeking a Process Validation Consultant to support sterile production processes. The ideal candidate will have experience with CGMP environments, qualification protocols, and risk assessments. Fluency in Italian and English is required. The role includes responsibilities such as conducting risk assessments, reviewing qualification protocols, and providing...
A healthcare organization is seeking a Validation Expert in Ivrea, Italy. This full-time role involves managing process validation activities and ensuring compliance with cGMP requirements. The ideal candidate will hold a scientific degree and have prior experience in a sterile GMP environment, alongside fluency in Italian and English. Key responsibilities include supporting validation planning,...
A global pharmaceutical company is seeking a candidate in Ivrea, Italy, to execute analyses on excipients, raw materials, and finished products. The role involves conducting stability studies, performing instrument qualifications, reviewing GMP documentation, and collaborating with various departments. The ideal candidate will possess a degree in chemistry and have experience in the...
A consulting firm in Ivrea, Italy is seeking a Process Validation Consultant to join its dynamic team. This role involves conducting risk assessments, supporting external suppliers, and ensuring compliance with CGMP standards. Ideal candidates will have experience in sterile production, qualification protocols, and a degree in Life Sciences or Engineering. Fluency in both Italian and English is...
Job Description Summary The Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. Job Description Major accountabilities : Support site validation planning by...
A consultancy firm in Piemonte is seeking a Process Validation Consultant to support sterile production processes. The ideal candidate will have experience with CGMP environments, qualification protocols, and risk assessments. Fluency in Italian and English is required. The role includes responsibilities such as conducting risk assessments, reviewing qualification protocols, and providing...
A leading global pharmaceutical company in Italy is seeking a Validation Expert to manage primary packaging and cleaning validation activities to ensure compliance with regulatory requirements. The ideal candidate will have a scientific degree, experience in a sterile GMP environment, and be fluent in Italian and English. Key responsibilities include supporting validation activities, risk...
Job Description Summary This role is responsible for architecting the structure and governance of data across key domains of the RLT (Radio Ligand Therapy) Supply Chain including Integrated Business Planning (IBP), Planning Logistics, Product Lifecycle Management (PLM) and Artwork. It ensures that data and its supporting frameworks are designed and integrated to enable operational readiness...
A leading global healthcare company in Italy is seeking to fill a full-time position focusing on data governance and architecture within the Radio Ligand Therapy Supply Chain. This role involves designing data frameworks, leading integration initiatives, and ensuring data integrity across key operational domains. Candidates should have a degree in a relevant field and solid experience in similar...
Job Description SummaryThe Pilot Plant Manufacturing Technician performs end-to-end production of radiopharmaceuticals in strict adherence to current Good Manufacturing Practices and approved Standard Operating Procedures ensuring quality sterility and regulatory compliance at every stage. It prepares handles operates and documents materials and equipment according to validated procedures...
A global healthcare company seeks a Regional Planning & Logistics Supervisor in Ivrea, Italy, to develop distribution plans for radiopharmaceuticals. This role involves managing supplier activities, ensuring compliance with GxP regulations, and collaborating with various stakeholders to maintain a continuous supply chain. The ideal candidate will have a degree in Science or Engineering, solid...