Technical Project Manager, CSL Vifor - Zurich

We are looking for a Senior Technical Project Manager to join our established team in Zurich, Switzerland. Reporting to the Head of Technical Project Management, you will be responsible for initiating, planning and executing strategic projects related to CMC Development, Continuous improvement, and Technology Transfer of parenteral pharmaceutical products and manufacturing processes. As Technical project manager for parenteral products, your responsibility includes the role of the manufacturing process subject matter expert. This role offers a diverse range of responsibilities and opportunities for professional growth.

Key Responsibilities

• Plan, implement, drive, and monitor projects for allocated brands/CMOs, ensuring deliverables, timelines, and budgets are met
  
• Support project work packages and tasks as subject matter expert for aseptic and terminal sterilized parenteral products manufacturing
  
• Facilitate effective communication throughout projects by proactively engaging in periodic calls and meetings
  
• Prepare comprehensive project as well as technical transfer plans, protocols and reports, including status updates, presentations, and meeting minutes, while defining and visualizing relevant KPIs

• Qualification in natural/life sciences or associated engineering degree (i.e. Biology, Biochemistry, Chemistry, Pharmaceutics, etc.), Bachelor/Master level or equivalent
  
• Experience in Project Management and Delivery in pharmaceutical, chemical or related industry
  
• Self-driven and fast learner with the ability to take ownership and lead projects independently
  
• Confident and proactive team player who collaborates effectively while working autonomously.
  
• Solid expert knowledge in sterile and aseptic fill & finish CMC development, Equipment -/Process Qualification & Validation, Manufacturing
  
• High Flexibility and willingness to travel & Experience in External Manufacturing Environment
  

• Familiarity with GMP requirements and Guidelines related CMC LCM activities, including Annex 1
  
• Know-how across various parenteral product primary packaging solutions (vials, ampoules, infusion bags)
  
• Experience in other Drug Product and Finished Product manufacturing & Technology Transfer, e.g. oral solid dosage forms
  
• Ability to work effectively in a multicultural and international environment
  
• Strong stakeholder engagement and cross-functional communication
  
• Strong communication and negotiation skills.
  
• Analytical thinking & problem-solving skills
  
• Ability to adapt to changing project requirements.
  
• Languages: English fluently, German is an advantage