Senior Technical Writer
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| Job Type | Contractor |
| Location | Dublin |
| Area | Dublin, Ireland |
| Sector | EngineeringOperations & Manufacturing |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | +353 1 574 6266 |
| Job Ref | 1002867 |
| Job Views | 41 |
- Description
- Team Horizon is seeking a Senior Technical Writer (initial 12-month contract) for our client who are a global leader in the biopharmaceutical industry based in Dublin.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
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.
Any other duties as assigned.
What you need to apply:
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.
