Remote CMC Regulatory Lead – Biologics

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 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 strategies...

Parexel in Italy (Catania area) is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biologics and vaccines.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...

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...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biological and vaccine products.Possiede le competenze, l'esperienza e la determinazione necessarie per avere successo in questo ruolo? Lo scopra qui sotto.This role involves post-approval regulatory activities, collaboration across manufacturing, QA, QC, and regulatory teams, and...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biologics and vaccines.Si assicuri che tutte le informazioni della sua candidatura siano aggiornate e corrette prima di cogliere questa opportunità.The role supports post-approval activities, variations, renewals, and market expansions, delivering timely regulatory assessments and...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics.È il candidato/la candidata ideale per questa opportunità? Lo scopra leggendo la panoramica del ruolo qui sotto.The role allows office or home-based work across Europe.You will develop submission strategies, assess...

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...

Overview In this role you drive analytical development for gene editing and nucleic acid-based therapeutics within the GRD CMC team. You lead method development and control strategies for complex modalities, including ATMPs and LNP-based products, collaborating across functions from candidate selection to clinical development and launch. You oversee...