Technical Project Manager Zurich

We are looking for a Technical Project Manager to join our established team in Zurich, Switzerland.

Reporting to the Head of Technical Project Management, you will be responsible for planning and executing projects related to CMC Development, optimization, and Technology Transfer of pharmaceutical products and manufacturing processes. 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

• Facilitate effective communication throughout projects by proactively engaging in periodic calls and meetings

• Prepare comprehensive project reports, including plans, status updates, presentations, and meeting minutes, while defining and visualizing relevant KPIs

• Build 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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