Contract start date: As soon as possible
Contract end date: ..6
Location: Visp
Responsibilities:
1. Answering customer requests for audit dates
2. Planning audits together with project teams, based on the customers’ agendas
3. Organising the required infrastructure (meeting rooms etc.)
4. Accompanying the customer throughout the audit (plant tours, documentation review etc.)
5. Presenting Quality systems to the customer
6. Coordinating with the project teams to ensure that all SMEs and documents requested by the customer are available in a timely manner
7. Documenting the audits in TrackWise
8. Coordinating the responses to audit observations with the project team and ensuring that the customer receives the responses within the given timelines
9. Work closely within different teams and with other departments
10. Must interpret and maintain proficiency in regulations, standards, guidelines and trends in cGMP.
Requirements:
11. Experience in pharma/biotech industry
12. Auditing experience
13. Understanding of the applicable cGMP regulations
14. General knowledge of manufacturing processes and analytical methods
15. Competent level of general IT skill is required
16. Ability to align cross functional stakeholders
17. Provide exceptional customer service by developing excellent working relationships with both external and internal customers