C&Q Technical Writer.

C&Q Technical Writer

Contract Duration: Initial 12-month contract

Role Overview

We are seeking an experienced Commissioning & Qualification (C&Q) Technical Writer to support the delivery of C&Q activities across GMP-regulated facilities, equipment, instruments and utilities.

The successful candidate will be responsible for preparing, reviewing and maintaining high-quality C&Q documentation to ensure that new installations and modifications to existing facilities, equipment, instruments and utilities are appropriately documented, commissioned and qualified, and that existing systems remain in a qualified state.

The role will involve close collaboration with Project Engineering, Maintenance, Operations and external engineering contractors to ensure C&Q activities are completed in accordance with applicable regulatory requirements, site procedures and industry standards.

Key Responsibilities

• Prepare, review and update C&Q documentation in accordance with approved templates, site procedures and regulatory requirements.
• Develop and maintain C&Q procedures, templates, standards and documentation processes to ensure consistency and efficiency.
• Prepare demolition, mechanical completion, Installation Verification (IV) and Operational Verification (OV) documentation.
• Develop and maintain risk assessments, Commissioning & Qualification Plans, Verification Plans, summary reports and User Requirements (UR) documentation.
• Ensure all C&Q documentation complies with relevant local and global corporate procedures, GMP requirements and applicable industry standards, including ISPE guidelines.
• Ensure C&Q protocols are executed in the correct sequence and closed out within agreed timelines.
• Provide day-to-day technical guidance to protocol executors and support the resolution of protocol-related queries.
• Register, track and manage discrepancies, following up on outstanding items through to closure.
• Represent the C&Q function on project teams, advising on C&Q requirements, documentation standards and project deliverables.
• Review engineering and C&Q documentation, providing guidance and coaching to technical staff on C&Q processes and best practices.
• Ensure personnel involved in C&Q activities are appropriately trained in relevant procedures and documentation requirements.
• Support the delivery of C&Q training courses as required.
• Update and maintain technical data within the Engineering Data Management System (EDMS).
• Coordinate the transfer of completed C&Q documentation into the site document library.
• Maintain C&Q databases to ensure documentation and qualification status are accurate and up to date.
• Support other GMP activities as required, including requalification protocols and Performance Qualification (PQ).
• Participate in and support internal, corporate and third-party audits as assigned.

Essential Skills and Experience

• Proven experience in C&Q technical writing within a GMP-regulated environment.
• Track record of supporting the delivery of GMP facilities and Commissioning & Qualification projects.
• Strong technical writing, documentation and computer skills.
• Excellent organisational skills and attention to detail, with a strong focus on accuracy.
• Ability to manage multiple tasks, prioritise workload and meet project deadlines.
• Strong interpersonal and communication skills, with the ability to work effectively across multidisciplinary teams.
• Ability to work independently and collaboratively within a project environment.
• Understanding of GMP requirements, C&Q documentation practices and applicable industry standards.

Desirable Skills

• Experience using the Regulus system.
• Familiarity with Engineering Data Management Systems and electronic documentation databases.
• Experience supporting C&Q audits, training activities and discrepancy management.
• Experience reviewing engineering documentation and supporting technical teams with C&Q processes.

Education and Qualifications

• Third-level qualification in Engineering, Science or a related discipline, or equivalent relevant industry experience.

Additional Requirements

• Flexibility to travel occasionally within Ireland or internationally for short periods to attend meetings, visit vendor facilities or undertake training.
• Ability to work closely with site teams, project engineering resources, contractors and operational stakeholders to support the successful delivery of C&Q activities.

Key Objective

To ensure that all Commissioning & Qualification documentation is accurate, compliant, appropriately executed and maintained, supporting the successful delivery of GMP projects and the continued qualified state of site facilities, equipment, instruments and utilities.