Senior Regulatory Affairs – CMC Biologics

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 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,...

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...

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,...

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 Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines, with remote options across Europe. You will collaborate with manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance across variations, renewals, and market expansions.The role...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines. You will collaborate with manufacturing, QA, QC and regulatory teams to shape submission strategies and support variations, renewals and market expansions, with remote options across Europe.Responsibilities include developing...

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...