Offerte di lavoro cmc – Roma

Select how often (in days) to receive an alert: Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT 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,...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines, with remote options across Europe.Continui a leggere per comprendere appieno cosa richiede questo lavoro in termini di competenze ed esperienza. Se il suo profilo è in linea, invii la sua candidatura.You will collaborate with...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines.Scorra la pagina per visualizzare tutti i requisiti del lavoro e le responsabilità che i candidati selezionati dovranno assumersi.You will collaborate with manufacturing, QA, QC and regulatory teams to shape submission strategies and...

PQE Group ricerca un Regulatory Affairs CMC Expert Consultant con 2-6 anni di esperienza per guidare sottomissioni regolatorie e strategie CMC. Ruolo in ibrido con mobilità nazionale/international e possibilità di lavoro da home office o uffici PQE Group.Laurea in discipline scientifiche; buona conoscenza delle norme ICH; autonomia, gestione di più...

Thermo Fisher Scientific seeks an experienced Regulatory Affairs professional to support EU/EEA regulatory assessments of changes for clinical trial documentation and related CMC activities.Interessato/a a questo ruolo? Può trovare tutte le informazioni pertinenti nella descrizione qui sotto.The role focuses on coordinating regulatory change control, SoC...

Parexel is seeking a Regulatory Affairs ConsultantÈ questo il ruolo che sta cercando? Se sì, continui a leggere per maggiori dettagli e si ricordi di candidarsi oggi stesso.- CMC vax/bio in Caserta, Italy, offering home or office based work.You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products...

Chiesi Farmaceutici S.p.A. in Parma, IT, seeks an experienced senior CMC leader for protein biologics drug substance development within GRD CMC. You will lead upstream/downstream development, analytical control strategies, comparability, and lifecycle management for recombinant protein therapeutics. The role requires deep CMC expertise, leadership of...

Parexel is seeking a Senior Regulatory Affairs Associate to lead post-approval CMC activities for biologics and vaccines.Le informazioni riportate di seguito illustrano i requisiti del ruolo, l'esperienza richiesta ai candidati e le qualifiche associate.You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biologics and vaccines. The role involves post-approval regulatory activities, worldwide submissions, and close collaboration with manufacturing, QA, QC, and regulatory teams to drive submission strategies and risk mitigation.This position supports variations, renewals, and market...

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 Regulatory Affairs 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 abbiamo la...

Parexel is seeking an Regulatory Affairs ConsultantScopra di più sui compiti quotidiani, le responsabilità generali e l'esperienza richiesta per questa opportunità scorrendo subito verso il basso.- CMC for post-approval activities related to vaccines or biological products.The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biological and vaccine products.È la persona giusta per questa opportunità? Si assicuri di leggere la descrizione completa qui sotto.You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies...

Chiesi Farmaceutici S.p.A. is seeking a GRD Technical Leader to manage budget, strategy, and execution for CMC development and IMP supply. The role directs ETT workstreams, collaborates with CT and product teams, and leads external partners to drive development milestones and regulatory approvals.The candidate will lead technical reviews, ensure...

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...

Work SchedulePotrebbe essere proprio lei il candidato/la candidata ideale per questo lavoro. Legga tutte le informazioni associate e invii la sua candidatura.Standard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin our global Regulatory Affairs team in a client-dedicated role supporting commercial medicinal products used in clinical trials,...

Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT 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...

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,...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biologics and vaccines. The role supports post-approval activities, variations, renewals, and market expansions, delivering timely regulatory assessments and risk mitigation. Remote options are available across several European locations, with collaboration across manufacturing, QA,...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biologics and vaccines. Vuole candidarsi? Legga tutte le informazioni su questa posizione qui sotto, poi prema il pulsante per candidarsi. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biological and vaccine products. This role involves post-approval regulatory activities, collaboration across manufacturing, QA, QC, and regulatory teams, and support for variations, renewals, and market expansions. Remote options in Europe are offered. The role emphasizes writing...