Job Description
A leading Biotech company in Dublin seeks an experienced Technical Writer for a 12-month hourly contract.
Main Responsibilities:
* Generate, review and update Standard Operating Procedures (SOPs).
* Collaborate with Manufacturing/Inspection/Engineering teams on documentation changes and updates.
* Develop protocols for execution in Manufacturing & Inspection to support change controls, deviations, and troubleshooting investigations.
* Manage change controls for Manufacturing/Inspection/Engineering.
* Liaise with Quality Assurance to ensure GMP standards are upheld at all times.
* Use specified software packages and standard procedures to compile and maintain relevant documentation, including SOPs.
* Provide technical and clerical support to the manufacturing, inspection, and engineering teams in documentation preparation, data collation, and SOP tracking.
* Owning minor deviations as required.
Basic Qualifications:
* Degree in Science or Engineering discipline.
* Significant experience in Chemistry/Microbiology/Engineering/Validation within a Biotech or Pharma industry.
* Experience working in a GMP environment.
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