Regulatory Technical Writer & Training Liaison

BioMarin Pharmaceutical Inc.; Cork; On-site; EUR 45,000 - 65,000; Full time

Job summary

BioMarin Pharmaceutical Inc. is seeking a Biologics Centre of Excellence Technical Writer to support regulatory documentation and training administration at Cork, Ireland.

The role requires writing high‑quality documentation in line with compliance standards and coordinating with technical SMEs to ensure accuracy and cross‑training. The ideal candidate will have a science/engineering background and proven experience in technical writing within regulated environments, contributing to inspection

Qualifications

• Third level qualification in a Science or an Engineering discipline.
• Proven experience in technical document writing.
• Familiarity with regulatory documentation and quality systems is advantageous.

Responsibilities

• Lead the ongoing enhancement of the documentation management strategy.
• Draft, review, and approve BPDs, SOPs, technical protocols & reports.
• Collaborate with SMEs to gain deep product knowledge for accurate documentation.

Skills

Technical writing

Regulatory documentation

Veeva systems

Education

Science or Engineering degree

Tools

Veeva Quality Documents

Compliance Wire

Job description

BioMarin Pharmaceutical Inc. is seeking a Biologics Centre of Excellence Technical Writer to support regulatory documentation and training administration at Cork, Ireland.

The role requires writing high‑quality documentation in line with compliance standards and coordinating with technical SMEs to ensure accuracy and cross‑training. The ideal candidate will have a science/engineering background and proven experience in technical writing within regulated environments, contributing to inspection