QC Specialist II

Job SummaryThe Technical Specialist II will be responsible for ensuring the smooth flow of samples produced in the Rieti plant, including products intermediates, critical fluids, stability, and raw materials, to perform testing for batch release.Key Responsibilities• Raw material sampling and testing (NIR)• Receiving and storage of product intermediates,...

Job Title: Technical Specialist IILocation: Rieti Responsabilità: Il dipendente esegue test microbiologici su materie prime, intermedi di processo, bulk product, verifica delle cleaning e campioni di monitoraggio ambientale. Inoltre, partecipa ad attività di validazione e contribuisce al mantenimento delle attività LeanLab e 5S.Richieste: Buona conoscenza...

Role:**  Proactive Quality Assurance Specialist with expertise in quality control, possessing knowledge of welding/fabrication, and experience with the application of relevant EN and ASME standards and NDT techniques.Responsibilities:  Preparation and sign-off of project final inspection release certificates, inspection test plans, and inspection and...

A proactive and results-driven Quality Assurance Specialist with a strong background in quality control and a passion for ensuring the highest standards of quality in welding and fabrication processes.The ideal candidate will have a deep understanding of EN and ASME standards, as well as NDT techniques, and be able to effectively communicate with suppliers...

Job Summary:We are seeking a highly skilled Quality Control Technician II to join our team at Takeda Pharmaceutical. As a key member of our laboratory team, you will be responsible for ensuring the quality of our products by performing various testing and sampling procedures.Key Responsibilities:Conduct raw material sampling and testing, as well as receiving...

Key Responsibilities:The Quality Assurance Specialist will be responsible for managing quality aspects and projects within their area of responsibility. They will ensure overall GxP conformity and compliance with the Novartis Quality Management Systems. This includes preparing documentation for batch release of commercial pharmaceuticals.Main...

TÜV SÜD è alla ricerca di un professionista qualificato per ricoprire il ruolo di Ispettore in ambito PED.La posizione è dedicata alla Divisione Industry Service, Real Estate & Infrastructure.Il candidato ideale dovrebbe avere esperienza nella gestione della qualità e nelle attività di progettazione e/o fabbricazione (industriale, apparecchiature in...

Sinergidea s.r.l. è un'azienda italiana specializzata nel settore IT/ICT, con competenza ed esperienza acquisite grazie a collaborazioni instaurate con realtà attive in diversi settori, come Banking, Finance, Industry, Automotive, Utilities, Energy. Ci distinguiamo sul mercato per i nostri servizi di consulenza e per le nostre soluzioni IT in area Digital...

Job Title: QC Clinical GCP SpecialistJefferson Wells is seeking a QC Clinical GCP Specialist on behalf of a pharmaceutical company based in Lombardia. The successful candidate will ensure that clinical trials are conducted in accordance with current national and international legislation, relevant guidelines, and the company's standard operating...

Main ResponsibilitiesAs a Quality Assurance Specialist at Novartis Farmacéutica, you will be responsible for overseeing all production and testing activities to ensure compliance with cGxP regulations, including data integrity and eCompliance.Key Accountabilities- Oversight of production and testing activities- Ensure compliance with cGxP regulations-...

Job Description:As a Quality Vendor Management Specialist at Thermo Fisher Scientific, you will play a crucial role in ensuring the general compliance of the mRNA site by providing strategic advice on licensing strategies applicable to the innovative mRNA product. Collaborate with our Customers, Quality, Supply Chain, Production, and QC teams to drive...

Job Summary-We are seeking a highly skilled Quality Assurance Specialist to manage quality aspects and projects within their area of responsibility. -The ideal candidate will ensure and support overall GxP conformity and compliance with the Novartis Quality Management Systems. About the Role Major accountabilities: Oversight of all production and testing...

Role OverviewWe are seeking a highly skilled Clinical Research Associate II to join our team at PSI CRO. As a Clinical Research Associate II, you will be responsible for conducting onsite monitoring visits, ensuring the highest quality standards in clinical research.Job DescriptionThis role offers an exciting opportunity to work on clinical studies in...

Job OverviewAllucent is a leading biopharmaceutical company that specializes in helping small-medium companies navigate the complex world of clinical trials. We are seeking an experienced Clinical Research Associate II to join our team and play a crucial role in ensuring the success of our clinical studies.

Job Title: Technical Completions SpecialistAs a Technical Completions Specialist, you will be part of a quality-focused team, ensuring projects are coordinated and managed through mechanical completion, pre-commissioning, and handover phases.Key Responsibilities:Manage the end-to-end commissioning process for mission-critical electrical, mechanical, and...

About Us:PSI CRO Ag is a leading Contract Research Organization with over 28 years of experience in the industry, offering a perfect balance between stability and innovation to clients and employees alike.We focus on delivering high-quality, timely services across various therapeutic indications, ensuring our clients receive exceptional results.Your Role:As...

Job OverviewA career-defining opportunity has emerged at the Healthcare Businesswomen's Association for a seasoned Quality Assurance Specialist with a deep understanding of environmental monitoring in the pharmaceutical industry/biotech sector. As we continue to drive excellence in quality management systems, we seek an individual who can effectively oversee...

About Agc IncAgc Inc is a global Contract Development Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way.Job OverviewWe are seeking an experienced Biopharmaceutical Quality Control Specialist to join our team in Copenhagen,...

**Ruolo**La nostra azienda, Istituto Geriatrico Milanese S.P.A., cerca un Specialista Contabilità Generale per affiancare la nostra squadra di professionisti.Compiti principali:• Gestione della partita doppia e contabilità clienti/fornitori;• Riconciliazione bancaria e gestione dei pagamenti;• Utilizzo del pacchetto Office per la gestione dei...

Job Summary:Adecco Italia S.P.A. is seeking a skilled Technical Commissioning Specialist to join our team. In this role, you will be responsible for managing the full commissioning process for mission-critical projects in electrical, mechanical, and control systems.Key Responsibilities:Manage the commissioning process from planning to handover, ensuring...