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UCB, one of Switzerland's Best Employers, is an internationally active biopharmaceutical company specialising in the therapeutic areas of neurological disorders and immunology. The Bulle site is home to the company's Swiss sales subsidiary and primarily a biotechnological and chemical production platform for the manufacture and distribution of pharmaceutical specialities for the treatment of allergy, epilepsy and autoimmune diseases.
Job Responsibility:
Strengthen the compliance culture at Bulle site through UCB and GMP standards
Actively participate in projects relating to Quality strategies
Represent the Quality Systems team internally
Actively contribute to simplification and streamlining of processes and support continuous Quality improvement initiatives
Write / approve / authorize Quality documentation and maintain / improve quality system procedures
Organize and participate in Quality committees
Help in organizing the quality management review on a quarterly basis
Perform weekly and monthly quality systems KPIs
Oversee governance, training deployment, and compliance of the process with UCB and GMP standards
Monitor process performance, report issues to management, and track action plans to ensure continuous improvement
Be responsible for the local process for the main quality systems (deviations management, CAPA management, investigation root causes management, QMS-Lifecycle management)
Requirements:
Minimum 5 years of professional experience in GMP-regulated industry, preferably within Quality Assurance or operational department
Strong autonomy, agility, and flexibility to manage multiple tasks and complex projects while meeting critical deadlines
Excellent leadership, coordination, and communication skills for effective collaboration
High level of discretion, negotiation, and persuasion abilities
Solid understanding of the GxP environment and expertise in writing scientific/technical documents
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