Regulatory Affairs Associate: EU Submissions & Publishing

Xeolas; Dublin; On-site; EUR 40,000 - 50,000; Full time

Job summary

A pharmaceutical company based in Dublin is seeking a Regulatory Affairs Associate to support regulatory publishing and submission activities. This role involves compiling regulatory dossiers, preparing and submitting documentation, and conducting quality reviews. The ideal candidate will have a Bachelor's degree in Health Sciences and 1-3 years of experience in the regulatory field. Strong attention to detail and organizational skills are essential. This permanent full-time position offers the opportunity to grow within a dynamic regulatory function.

Qualifications

• 1-3 years of experience in the pharmaceutical regulatory industry.
• Solid understanding of applicable regulations and guidance documents.

Responsibilities

• Support the compilation of regulatory dossiers for submissions.
• Assist in the preparation and submission of regulatory documentation.
• Conduct quality reviews of submission documents.
• Manage project workflows throughout the submission lifecycle.

Skills

Regulatory affairs principles

Attention to detail

Organizational skills

Ability to manage multiple priorities

Education

Bachelor's degree in Health Sciences or a related field

Job description

A pharmaceutical company based in Dublin is seeking a Regulatory Affairs Associate to support regulatory publishing and submission activities. This role involves compiling regulatory dossiers, preparing and submitting documentation, and conducting quality reviews. The ideal candidate will have a Bachelor's degree in Health Sciences and 1-3 years of experience in the regulatory field. Strong attention to detail and organizational skills are essential. This permanent full-time position offers the opportunity to grow within a dynamic regulatory function.