Job Responsibilities Support all quality-relevant packaging processes and collaborate with packaging operations and all relevant interfaces with regard to GMP topics. Partner with stakeholders and provide GMP support to ensure successful delivery of the company goals. Review and release manufacturing specifications and Batch Records (BR) of finished and semi-finished goods. Manage actively Deviations and Changes. Collaborate on the management of local and global projects and engage in optimization activities and improvements within IMP Quality Clinical Packaging Switzerland. Coordinate improvement projects and engage in corrective and preventive measures (CAPA). Build, verify, and implement standard documents (SOPs). Promote a human-centered and self-managed way of working based on New Work, focusing on supporting ongoing cultural and organizational changes towards collaboration, agility, and an innovation mindset. Minimum Qualifications Min. Master Degree preferably in Life Sciences or Engineering or similar degree. Solid experience in the pharmaceutical industry in a quality manager role. Knowledge of c GMP and quality requirements for clinical development phases. Experience in pharmaceutical development such as packaging lines or materials, master data management, quality control, or quality assurance is an advantage. Proven track record of working towards outcomes and an innovative manner of solving problems. Strong team player with a high level of self-motivation and the ability to inspire others. Ability to work in a purpose-driven organization, taking full ownership of assigned roles and tasks, continuously willing to improve individual and team effectiveness. Ability to communicate clearly and professionally verbally and in writing in BOTH German and English is necessary. Experience with SAP and Veeva is an advantage. Company Overview A very renowned company where you will work in an international environment.
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