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...
SummaryLocation: Ivrea, Italy #onsiteRole PurposeThis role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia.About The RoleKey responsibilities:Executes analyses on excipients, raw materials, finished products, and packaging...
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...
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...
Chi siamo: BDO è una società di consulenza e servizi professionali che da oltre 50 anni affianca imprese di ogni dimensione, dalle piccole e medie aziende ai grandi gruppi internazionali, fino a investitori privati e istituzioni pubbliche. Con una forte presenza in 164 paesi e più di 1.300 professionisti in Italia, la nostra azienda offre soluzioni integrate e personalizzate per ottimizzare la...
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...
La divisione Permanent Recruitment di Adecco Italia SpA - dedicata alla Ricerca&, Selezione di profili specializzati - ricerca: Responsabile di Produzione. La figura selezionata sar il cuore pulsante della gestione produttiva, con un ruolo chiave nel garantire l'efficienza degli impianti e il rispetto degli standard aziendali. Sarai chiamat* a lavorare in stretta collaborazione con diverse...
At InnovHeart we are developing transcatheter mitral valve replacement (TMVR) systems to treat patients suffering from mitral valve disease. With a view to expanding the workforce and insourcing this role, we are looking for a Program manager who will be primarily responsible for the projects by integrating and coordinating the contributions of all the actors and stakeholders.Responsibilities-...
TEMPOR SPA, Agenzia per il Lavoro, Filiale di Ivrea, seleziona per importante azienda cliente del settore Elettronico:ADDETTO QUALITA' E AMBIENTE- Definizione della politica aziendale ed accertamento che questa sia compresa ed attuata a tutti i livelli e da tutto il personale dell'azienda;- Cura la distribuzione controllata del MGA a tutti i destinatari, interni ed esterni, individuati dalla...
Summary Location: Ivrea, Italy. Please note that you will need to be able to commute to Ivrea as no relocation is on offer for this role. Hybrid. Role Purpose Act as Isotope Project Lead (IPL) by providing specialist knowledge and expertise as a subject‑matter expert (SME) of radioisotope production and purification. Focus on assessing, developing, and optimizing new technologies that support...
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 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...
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...
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 in Ivrea is seeking a dedicated Pilot Plant Manufacturing Technician to oversee the end-to-end production of radiopharmaceuticals. The successful candidate will ensure compliance with Good Manufacturing Practices and manage documentation. Applicants should possess technical education, at least 2 years of relevant experience, and a strong understanding of production...
Summary:The QC Supervisor supports the QC Head to ensure that Quality Control processes for materials acceptance, batches quality control and QC equipment validation/qualification are executed and fully compliant to cGMPs regulation, corporate and national guidelines.About the Role:Major accountabilities:- Be the Deputy of QC Head in managing, coordinating and approving the execution of the...