Offerte di lavoro cmc – Torino

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.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...

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...

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 Consultant - 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 within a regulatory team.You will collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant...

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...

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...

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 an Regulatory Affairs Consultant - CMC for post-approval activities related to vaccines or biological products. The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely regulatory outcomes.You will support worldwide regulatory activities, manage regulatory information systems, and...

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...

Parexel is seeking a Senior Regulatory Affairs Associate to 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. Responsibilities include developing post-approval CMC submission...

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...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biologics and vaccines. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. The role supports variations, renewals, market expansions, and annual reports,...

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,...

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,...

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 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...

Nouryon, a global leader in sustainable chemical solutions, seeks a Business Development Manager Textile EMEA to drive growth across Surfactants, CMC, and Chelates. You will manage key customer and distributor relationships, identify new opportunities, and execute initiatives to increase market share and profitability.You will combine technical expertise...

Parexel seeks a Regulatory Affairs Consultant Faccia ora il prossimo passo nella sua carriera: scorra verso il basso per leggere la descrizione completa del ruolo e invii la sua candidatura. - CMC vax/bio to support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to...