Description
Reference Nr.: 915538NC
Sector: Pharmaceutical
Location: Limerick
Start: ASAP
Duration: 2 months ++
Job Type: Contract
Initial Assignment:
- Complete a retrospective review of software components to update existing trace Matrix to have full URS/FDS/Test case reference coverage
- Identify gaps in the light of the current usage of this component
- Complete a full review of existing documentation relating to a 3rd party system supporting regulated and nonregulated systems.
Skills/Experience:
- 2-3 years' experience in validation and support of pharmaceutical laboratory instrumentation and systems
- Knowledge of GMP compliance as applied in the pharmaceutical industry, especially those related to document control, deviations/CAPA, training, and complaints.
- Experience in writing validation protocols and reports for software of GxP systems
- Strong project lead skills to develop clear project plans and to complete projects within agreed timelines.
- Good team player, organised, accurate, have strong documentation skills
- Passionate about quality and client service
- Good communication skills both internally and externally.