IMP Quality Clinical Packaging Specialist (m/f/d)

Location: Kaiseraugst

Start date: Immediately

End date: 31.05.2026/possible extension

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 of manufacturing specifications and Batch Records (BR) of finished and semi-finished goods
• Manage actively Deviations and Changes
• Collaboration through to the management of local and global projects
• Actively 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)
• Joy in a human-centered and self-managed way of working based on NewWork, with a key focus to support the ongoing cultural and organizational change towards collaboration, agility and innovation mindset

Requirements:

• Min. Master Degree preferably in Life Sciences or Engineering or similar degree
• Fluent in both German and English is mandatory
• Min. 3 years of experience in the pharmaceutical industry in a quality manager role
• Knowledge of cGMP and quality requirements for clinical development phases
• Experience in the area of pharmaceutical development such as packaging lines or materials, master data management, quality control or quality assurance is an advantage