Tech Writer

PE Global (UK); Dublin; On-site; EUR 55,000 - 85,000; Full time

Job summary

PE Global are recruiting for a Technical Writer for our biopharmaceutical client based in Dun Laoghaire, Dublin. This is a 12-month contract role with hybrid working options.

The role focuses on developing, updating and maintaining GMP documentation, SOPs and change controls, with collaboration across Manufacturing, QA and Engineering. Strong writing skills and cGMP knowledge are essential. You will own document control activities and support training materials to ensure regulatory readiness.

Qualifications

• Bachelor’s degree in science or engineering and 3+ years in biotech/pharma environments.
• Strong GMP documentation experience including investigations, procedures and change controls.
• Experience with regulatory compliance and cGMP manufacturing/testing is advantageous.
• Excellent written and verbal communication with ability to present technical data clearly.
• Ability to manage multiple tasks and deliver high-quality documentation on schedule.

Responsibilities

• Develop, update and maintain Operations procedures and SOPs; act as document owner.
• Liaise with Manufacturing, Inspection and Engineering on documentation changes in a timely manner.
• Develop protocols for manufacturing change controls and investigations with SMEs.
• Engage in continuous process improvement and troubleshooting projects.
• Own change controls and manage deviations and associated documentation.

Skills

Project management

Technical writing

Communication skills

Independent working

Cross-functional teamwork

Education

Bachelor’s degree in a Science or Engineering discipline

Job description

The Role

PE Global are recruiting for a Technical Writer for our biopharmaceutical client based in Dun Laoghaire, Dublin. This is a 12‑month contract role. Hybrid working options.

Job Responsibilities

• Develop, update and maintain Operations procedures in accordance with site and corporate requirements. Serve as a document owner. Assist in the generation of training materials and may assist in providing training on scientific or technical aspects of the process.
• Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner.
• Develop protocols for execution in Manufacturing & Inspection in support of change controls, non‑conformances & troubleshooting investigations with support from relevant SMEs.
• Involvement in projects as part of continuous process improvement and/or troubleshooting.
• Ownership and management of change controls as required.
• Issuance and updates of paper batch records in line with production schedule.
• Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current OS.
• Partner with Operations lead/appropriate SME to ensure updates are correct and aligned with project deliverables/ timelines.
• Perform document trending upon project completion to identify key issues/mistakes in document processing.
• Support data verification of Operations‑owned protocols, reports and risk assessments.
• Support the production support team in reducing document turnaround times.
• Use specified software packages and standard procedures, responsible for compiling and maintaining all relevant documentation including SOPs.
• Provide technical and clerical support to the manufacturing, inspection & engineering teams in the preparation of documentation, collation of data and tracking of SOPs.
• Ensure non‑conformances are triaged within the established goal and serve as a deviation owner for minor deviations.
• Own corrective/preventive actions and effectiveness verification.
• Support execution of C&Q, characterisation, functional testing protocols as required by project.

Education and Experience

• Bachelor’s degree in a Science or Engineering discipline.
• 3+ years of experience in Chemistry, Microbiology, Engineering or Validation gained within a biotech, pharma or healthcare organisation.
• Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products is an advantage.
• Strong project management and organisational skills, including the ability to follow assignments through to completion.
• Excellent verbal and written communication skills: strong technical writing skills for GMP documentation, such as investigations, procedures and change controls, and good presentation skills.
• Escalate issues professionally and in a timely manner.
• Ensure compliance within a regulatory environment.
• Demonstrated ability to work independently and deliver right‑first‑time results under minimal direction.
• Experience participating in and leading cross‑functional teams.
• Experience in managing multiple competing priorities in a fast‑paced environment.

Interested candidates should submit an updated CV.