About us The Clinical Trial Manager (CTM) is responsible for supporting the planning, set-up, conduct and close-out of one or more assigned clinical trials within CatalYm’s clinical development team. The CTM works closely with internal team members (including Sr. CTMs and CTAs), external vendors, collaboration partners and clinical trial personnel to ensure successful trial execution. The CTM is part of the Clinical Sub-team and reports to the Director Clinical Operations responsible for the respective program. Head of Quality Assurance (m/f/d) Festanstellung, Vollzeit · CatalYm GmbH As the Head of Quality Assurance at CatalYm, you will oversee all Quality Assurance activities in clinical development comprising all aspects of GxP governed processes with a main focus on GMP and GCP including Clinical Safety. You will be responsible for establishing and maintaining a strong Quality Management System and implementing quality oversight strategies ensuringe regulatory compliance and at the same time fostering a culture of quality and continuous improvement. Your tasks and responsibilities Lead the QA department and take ownership of the quality management system (QMS) covering all GxP areas Exploring the needs for a transition to an electronic QMS solution and driving the decision making process Develop risk-based approaches to quality management in the GxP environment Oversee the planning and execution of internal and external audits across all GxP areas Ensure inspection readiness across all departments governed by GMP and GCP Primary addressee for managing regulatory GxP inspections Align with C-level executives on quality initiatives required for inspection readiness Manage relationships with regulatory agencies and represent the company in quality-related matters Advanced degree in life sciences, pharmacy or medicine with 10 years of experience in pharmaceutical/biotech at least 5 years of those in Quality Assurance or Compliance A clinical development background is required Experience in preparing for and managing regulatory inspections Comprehensive knowledge of global GxP regulations, with main expertise in GCP Strong leadership skills with the ability to to work in a matrix setting Excellent analytical and problem-solving skills Fluent in English with excellent oral and written skills; good command of German. Flexibility for travel on an as needed basis Contribute directly to the success of cutting-edge oncology programs. Be part of an agile, collaborative biotech environment with visible impact. Enjoy flexibility, ownership, and professional growth within a supportive culture. 1-2 days home office per week