08 set - Parma
Gsk
Site Name: Italy - Parma
Posted Date: Feb 23 2026
- We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual premio based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme._
- We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work._
- Discover more about our company wide benefits and life at GSK on our webpage _Life at GSK | GSK_
Scope
The Established Sterile Investigation Team Coordinator assures an effective management of the team to assure the overall quality and effectiveness of the deviation, CAPA and complaints within established sterile department (FD, SHCF, FD Inspection) and ensures best practices are in place and in use, seeks for continuous improvement. Ensures capabilities buildup within the team through effective coaching and monitoring.
Direct Reports: 8 people
_ In this role,
You will:_
- Ensure suitable management of deviation and investigation and adherence to due date
- Responsible to guarantee management of deviations through adequate root cause analysis and identification of effective CAPAs
- Focus on people development within the team
- Ensure effective collaboration with all parties involved in Deviation and CAPA management (Msat, maintenance, engineering, operations)
- Responsible for the effectiveness of Deviation and CAPA end to end process and customer complain investigation
- Co-responsible with Production Departments for the progressive reduction of deviation through adequate root cause analysis and implementation of effective CAPA
- Ensure adequate KPI and governance are in place and in use to monitor, track and drive progress (i.e. human errors, recurrent deviations, deviation overdue, CAPA overdue, CAPA effectiveness checks)
- Escalate risks, issues and p
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