Regulatory Affairs Specialist — EU/US Submissions (Dublin)

Xeolas Pharmaceuticals; Dublin; On-site; EUR 65,000 - 95,000; Full time

Job summary

Xeolas Pharmaceuticals, based in Dublin, Ireland, seeks a qualified Regulatory Affairs Specialist for a permanent full-time role. The position involves managing regulatory dossiers, submissions, and interactions with Health Authorities across EU/US/ROW regions.

You will coordinate with cross-functional teams and external partners, ensuring on-time submissions and regulatory compliance while staying current with evolving guidelines and industry best practices.

Qualifications

• Masters/ Bachelor’s degree or equivalent in Science/Technology/Pharmacy.
• Minimum 5 years of Experience in Regulatory.
• Capable of understanding health authority expectations for pharmaceuticals for EU/US/ROW regions.
• Must possess organization skills, time management skills and attention to detail.
• Excellent critical thinking and problem-solving abilities.
• Strong interpersonal and communication skills.
• Experience in dealing with multiple stakeholders, both internal and external.

Responsibilities

• Preparation and maintenance of high quality dossiers (marketing authorisation applications/ Response to Health authority questions/ post-approval submissions).
• Submission of CPP/ Manufacturing authorisation requests to HPRA/MHRA
• Review of data intended for submission and advise regarding any deficiencies or issues.
• Ensure on-time submissions for all quality/ safety related changes for assigned projects.
• Preparation and submission of translated texts to EU/Non-EU countries
• Update of databases and systems for all products (in-line with current SOPs)
• Liaise with 3rd parties (where required) to establish effective communication and relationships in order to progress regulatory activities.
• Liaise closely with Business Development, Product Launch, Artwork, Supply Chain and Quality colleagues to ensure alignment in all initiatives.
• Advise management of the status and progress of assigned projects identifying potential problems or delays, and possible solutions, as they occur and maintain a current status report for these projects.
• Maintain an awareness of regulatory requirements (including legislation, guidelines, industry best practice, and through liaison with competent Authorities) and use this information to optimise departmental procedures and processes and to ensure Health Authority requirements and Regulatory Compliance are maintained.

Skills

Regulatory Affairs

Project management

Communication

Attention to detail

Stakeholder management

Education

Master's or Bachelor's degree in Science/Technology/Pharmacy

Job description

Xeolas Pharmaceuticals, based in Dublin, Ireland, seeks a qualified Regulatory Affairs Specialist for a permanent full-time role. The position involves managing regulatory dossiers, submissions, and interactions with Health Authorities across EU/US/ROW regions.

You will coordinate with cross-functional teams and external partners, ensuring on-time submissions and regulatory compliance while staying current with evolving guidelines and industry best practices.