Senior Regulatory Affairs, CMC

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. 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 and...

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,...

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...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe.You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join our global Regulatory Affairs team in a client-dedicated role supporting commercial medicinal products used in clinical trials, including comparator and auxiliary medicinal products. This highly client-facing position combines EU/EEA regulatory assessment, CMC and labelling...

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 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,...

Parexel seeks a Regulatory Affairs Consultant - 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 shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers.The role emphasizes...