This is a fantastic opportunity to be part of a fast-paced, €700 million project; with lots of opportunities to work with and learn about cutting-edge technologies, in addition to developing your own skills.
This is a truly exciting project, which when complete will contribute to the manufacturing of a life changing treatment.
Essential Duties and Responsibilities for this Documentation Co-ordinator role include, but are not limited to, the following:
- Responsible for the scanning, uploading and management of documentation within the Documentation Management system (MIDAS/QualityDocs).
- To support document generation, review, approval of documentation within the Documentation Management system e.g., SOP's, WI's, and related GMP documentation
- Format, write, deliver and review necessary documentation in line with the standard approval process, and facilitate others to do so.
- Support site activities through documentation generation, filing, tracking, auditing and maintenance of associated logs/databases.
- Support QA department in generation of meeting Agendas and collation of meeting minutes actions and related duties.
- Presentation, compilation and review of Quality-related data as directed.
Desirable Experience for this Documentation Co-ordinator are:
- Experience in the Pharmaceutical or Biological industry.
- Highly motivated, and results focussed.
- Knowledge of GMPs
- Good presentation and social skills
- Previous experience working in a Documentation or Administration role.
- Experience with MIDAS/QualityDocs would be advantageous.
Job – Documentation Co-ordinator
Job type – Contract
Duration – 6 months (likely extension)
Start date – ASAP
Location - Dublin
If you’ve got the above experience and would like to be considered for this role, please apply now.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta Consultancy Services does not sponsor Visa applications.
As Dublin continues to embed itself as Irelands Pharmaceutical capital, we are seeking a QA Specialist to become part of a $500 million state of the art bio facility. Located 15 minutes from Dublin
As Dublin continues to embed itself as Irelands Pharmaceutical capital, we are seeking a Documentation Specialist to become part of a $500 million state of the art bio facility. Located 15 minutes
Ireland is a hive of activity for the Life Sciences Industry at present with many major pharmaceutical companies investment in new facilities here in recent years. We currently have a number of
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