Location: Visp
Workload: 100%
Contract end date: November 2025
Responsibilities:
* Provide a safe, controlled work environment in all areas of responsibility
* Work with Stakeholders to ensure cGMP compliance in all aspects of the GMP deliverables under its accountability
* Collaborate with stakeholders and SMEs e.g Ops BPEs, MSAT group, Engineering, QC to bring about process robustness/ improvements to routine manufacturing via CAPA strength
* Responsible for meeting assigned deviation investigations timelines, acting as investigation lead when required, to meet production and batch release schedules while ensuring appropriate level of investigation quality
* Create, review and approve deviation investigation reports, CAPAs etc. to ensure consistency and high standards in technical investigation and writing
* Change request manager for Mfg Operations when designed
* Support on GMP documentation management (review, DMS workflows) of Mfg Operations
* SME from Ops area during audits or customer meetings for the deliverables in scope of accountability
Requirements;
* 5-10 years in cGMP regulated environment, MFG
* Fluent German
* Excellent leadership skills in team based management
* Strong communication and interpersonal skills
* Analytical thinking and problem solving skills
* High adaptability in dynamic work environments
* Effective and efficient time management
* Knowledge of Microsoft Windows and Microsoft Office (Excel, Word, Project, PowerPoint)
#J-18808-Ljbffr