Technical Writer

PE Global (UK)

Cork

On-site

EUR 55,000 - 65,000

Full time

14 days+
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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

The Role

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. Hybrid working options.

Job Responsibilities
  • Lead, develop, and drive the ongoing enhancement of the documentation management strategy
  • Produce high-quality, accurate documentation by applying data integrity and ALCOA principles, adhering to compliance best practices, and ensuring all materials are appropriate for their intended audience
  • Serve as Subject Matter Expert (SME) for Veeva Quality Documents & Compliance Wire, offering guidance and support to colleagues in the use of these systems
  • Draft, review, and approve BPDs, SOPs, technical protocols & reports, forms, work instructions, and other document types
  • Collaborate closely with technical SMEs and teams to gain deep business and product knowledge for accurate documentation requirements
  • Demonstrate excellent verbal and written communication skills to engage and motivate diverse audiences
  • Propose and implement continuous improvements to the technical writing process, such as developing Advanced Templates
  • Support Technical Writing activities across the site and collaborate with various departmental SMEs
  • Manage the transition of documentation into Veeva Quality Documents and initiate Change Requests as necessary
  • Support Global Training &/or Bus Ops with BcoE training development programs and materials, guides, and e-learning modules to address identified learning requirements
Education and Experience
  • Third level qualification in a Science or an Engineering discipline, and/or extensive related proven experience in the required areas: technical document writing

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland****

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