Biotech Technical Writer — Hybrid, Documentation Lead

PE Global (UK); Cork; Hybrid; EUR 55,000 - 65,000; Full time

Job summary

PE Global are recruiting for a Technical Writer for our biotechnology client based in Ringaskiddy, Co. Cork. This is an initial 12-month contract role with hybrid working options.

Key duties include developing and driving the documentation management strategy, producing high-quality documents using ALCOA principles, and acting as SME for Veeva Quality Documents & Compliance Wire. Collaboration with technical SMEs and teams is essential to ensure accurate documentation across BPDs, SOPs,

Qualifications

• Third level qualification in a Science or Engineering discipline or extensive related experience in technical writing.
• Experience producing high-quality documentation with data integrity and ALCOA principles.
• Experience with documentation management systems (Veeva Quality Documents) is desirable.

Responsibilities

• Lead enhancement of the documentation management strategy.
• Produce high-quality, accurate documentation applying ALCOA principles and compliance best practices.
• Serve as SME for Veeva Quality Documents & Compliance Wire and guide colleagues.
• Draft, review, and approve BPDs, SOPs, technical protocols and reports.
• Collaborate with technical SMEs to gain deep product knowledge for documentation requirements.
• Demonstrate strong verbal and written communication to engage diverse audiences.
• Propose improvements to the technical writing process, including templates.
• Support Technical Writing activities across the site with SMEs.
• Manage the transition of documentation into Veeva Quality Documents and initiate Change Requests.
• Support training development programs and materials to address identified learning requirements.

Skills

Technical writing

Documentation management

Communication

Education

Science/Engineering degree or related experience

Tools

Veeva Quality Documents

Compliance Wire

Job description

PE Global are recruiting for a Technical Writer for our biotechnology client based in Ringaskiddy, Co. Cork. This is an initial 12-month contract role with hybrid working options.

Key duties include developing and driving the documentation management strategy, producing high-quality documents using ALCOA principles, and acting as SME for Veeva Quality Documents & Compliance Wire. Collaboration with technical SMEs and teams is essential to ensure accurate documentation across BPDs, SOPs,