Contract start date: As soon as possible
Contract end date: 31.03.2026
Location: Visp
Responsibilities:
* Answering customer requests for audit dates
* Planning audits together with project teams, based on the customers’ agendas
* Organising the required infrastructure (meeting rooms etc.)
* Accompanying the customer throughout the audit (plant tours, documentation review etc.)
* Presenting Quality systems to the customer
* Coordinating with the project teams to ensure that all SMEs and documents requested by the customer are available in a timely manner
* Documenting the audits in TrackWise
* Coordinating the responses to audit observations with the project team and ensuring that the customer receives the responses within the given timelines
* Work closely within different teams and with other departments
* Must interpret and maintain proficiency in regulations, standards, guidelines and trends in cGMP.
Requirements:
* Experience in pharma/biotech industry
* Auditing experience
* Understanding of the applicable cGMP regulations
* General knowledge of manufacturing processes and analytical methods
* Competent level of general IT skill is required
* Ability to align cross functional stakeholders
* Provide exceptional customer service by developing excellent working relationships with both external and internal customers
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