• Bachelor’s or Master’s degree (or higher) in Biotechnology, Pharmaceutical Sciences, Engineering, or related field.• 12+ years of progressive experience in Quality Control, Analytical Operations, or Technical Operations within a biotechnology or pharmaceutical company.• Demonstrated leadership in developing and managing operational systems in GMP-regulated environments.• Strong understanding of cGMP, global regulatory requirements, and analytical testing operations.• Proven ability to design and implement business processes, governance models, and performance management systems.• Experience with vendor management and collaboration with CDMOs/CROs on analytical testing and QC operations.• Exceptional communication, negotiation, and relationship-building skills with internal and external stakeholders.• Strong analytical, organizational, and problem-solving skills; adept at data-driven decision-making.• Demonstrated passion for process improvement, operational efficiency, and automation
• Reports to: Head of Quality Control
• Reports to:
• Location: Visp, Switzerland
• Location:
• Compensation:The compensation package will be competitive and includes an equity component.