GMP Operations Support (m/f/d)

Location: Visp

Workload: 100%

Contract duration: 6 months

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
• 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)