The Role

PE Global are recruiting for a Technical Writer for our biopharmaceutical client based in Dun Laoghaire, Dublin. This is an 11-month contract role. Hybrid working options.

Job Responsibilities

Develop, review and update engineering, manufacturing, & inspection Standard Operating Procedures.
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, deviations & troubleshooting investigations with support from relevant SMEs.
Involvement in projects as part of continuous process improvement and / or troubleshooting,
Ownership of change controls for Manufacturing/Inspection/Engineering
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current OS
Support 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
Ownership of minor deviations as required

Education and Experience

Educated to degree level or equivalent.
Significant experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organisation.
Experience working in a GMP environment
Project management experience is desired

Interested candidates should submit an updated CV.

Please click the link below to apply or alternatively send an up-to-date CV to

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

Salary Criteria