Offerte di lavoro qc validation – Genova

Recordati cerca Analista Controllo Qualità per eseguire analisi chimiche, fisiche e microbiologiche su materie prime, semilavorati e prodotti finiti, garantendo conformità agli standard GMP e alle normative vigenti. Si richiede laurea in chimica o titolo equiparabile e esperienza in QC farmaceutico.La figura lavorerà nel laboratorio, gestirà strumenti...

Attività principali:Stesura e revisione documenti GMP per Process Validation, quali PPQ Master Plan, PPQ protocol e report, protocolli e report per studi supportivi alla validazione, gap e impact assessment report, analisi del rischio e identificazione parametri critici di processo, valutazione specifiche di processo e analitiche, raccolta e analisi dati....

Mansione Randstad Italia Spa, filiale di Mosciano Sant'Angelo, è alla ricerca per importante azienda farmaceutica di un analista chimico di laboratorio QC Impegno di lavoro full time, su due turni Iniziale inserimento in somministrazione di lavoro con livello D3 CCNL Chimico farmaceutico. Sede di lavoro: Teramo Responsabilità La risorsa si occuperà...

Job DescriptionJob descriptionAre you registered as a member of a protected category under Italian Law 68/99? Join our team as QC Chemistry 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.Your missionsPerform chemical analysis using HPLC with...

Job DescriptionJob descriptionAre you registered as a member of a protected category under Italian Law 68/99? Join our team as QC Chemistry 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.Your missionsPerform chemical analysis using HPLC with...

Overview As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. Your work supports variations, renewals, and market expansions,...

Overview In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across...

FILIALE: MONZASPECIALIZZAZIONE: CORE SKILL - Life ScienceGrafton LifeScience* is a dedicated team focused on enhancing the experiences, skills, and potential of candidates in Sales & Marketing, Clinical Research, Regulatory, and Operations within the Pharmaceutical and Medical sectors. We also specialize in roles related to customer support in the...

Milano, ITL’Analista Controllo Qualità è responsabile dell’esecuzione delle analisi chimiche, fisiche e/o microbiologiche su materie prime, semilavorati e prodotti finiti, al fine di garantire la conformità agli standard di qualità richiesti e alle normative vigenti (GMP, ISO, ecc.). La figura opera nel rispetto delle procedure aziendali e delle...

Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dell’industria farmaceutica e dei Medical Device?In PQE Group, la nostra divisione di Laboratory Excellence è sempre in una fase di grande crescita grazie ad un mercato in continua evoluzione che sempre più richiede la qualità dei nostri servizi. Per questo motivo...

Sei pronto ad entrare in una realtà internazionale che sta ridefinendo gli standard dell’industria farmaceutica e dei Medical Device?In PQE Group, la nostra divisione di Laboratory Excellence è sempre in una fase di grande crescita grazie ad un mercato in continua evoluzione che sempre più richiede la qualità dei nostri servizi. Per questo motivo...

Overview In this role, you will support quality control testing of raw materials, intermediates, and finished products to ensure compliant release and stability data. You will work within Sampling & Analysis to uphold cGLP, perform instrumental analyses (HPLC, GC, UV-Vis, etc.), and maintain rigorous documentation and audit readiness. You’ll contribute to...

Overview The role is a senior-level position within the Global Manufacturing Science & Technology (MS&T) department at the Menarini Group, based in Florence. Reporting directly to the Global MS&T Lead, the manager acts as a strategic technical bridge between R&D, Manufacturing, Quality, Regulatory Affairs, Supply Chain, and CMOs. The primary mission is to...

As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. Your work supports variations, renewals, and market expansions, delivering...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

Data Analysts, Data Quality & Business Data Review Specialists.Remote AI ProjectScorra verso il basso per una panoramica approfondita di questo lavoro e dei requisiti per i candidati.Invii la sua candidatura facendo clic sul pulsante "Candidati".We are seeking experienced Data Analysts, Business Data Analysts, Data Quality Specialists, Data Reviewers, and...

pbUnited States or Italy | Remote | Full-time /b /p h3About Valos /h3 pValos is an international biometrics CRO providing Biostatistics, Statistical Programming and Clinical Data Management services to pharmaceutical, biotechnology and medical device companies./p pWe are building the next stage of our Statistics organization and are looking for a bPrincipal...

As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. Your work supports variations, renewals, and market expansions, delivering...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...