#R-251501
ld and manage high-performing, crossfunctional teams, implementing complex projects and initiatives at external and internal manufacturing sites
Serve as the key technical interface for external partners and contract manufacturing organizations on allocated projects/brands
Support and drive the evaluation of alternative, cost-effective sourcing strategies for API, DP, starting and raw materials by coordinating technical development work, vendor evaluation
Ensure proposed and established sourcing strategies align with corporate and brand strategies as set forth by governing bodies
Conduct due diligence visits at potential future contract manufacturing organizations
Travel to contract manufacturers to monitor project progress, support implementation, and troubleshoot as needed
Provide adequate background information, documentation, and technical advice to decision bodies and negotiation teams to ensure timely decision-making
Support the achievement of goals and targets for the respective brand organization
Skills & Experience
Minimum Requirements
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
High Flexibility and willingness to travel
Experience in sterile and aseptic fill & finish CMC development, Equipment -/Process Qualification & Validation, Manufacturing
Preferred Requirements
Familiarity with GMP requirements and Guidelines related CMC LCM activities
Experience in Drug Product and Finished Product manufacturing & Technology Transfer
Know-how across various parenteral product primary packaging solutions (vials, Ampoules, Bags)
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
This is a hybrid role based in Zurich, Switzerland
Closing date for Applications Monday 26th May 2025
About CSL Vifor
CSL Vifor aims to become the global leader in iron deficiency and nephrology.
The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care.
For more information, please visit viforpharma.com
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