Job Description

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 Build and manage high-performing, cross functional 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 for assigned projects and brands, as well as for defined topics in routine manufacturing, including coordination and support in case of technical issues, process changes, deviations, and improvement initiatives 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 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
Preferred Requirements


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
Are you interested? We are looking forward to receiving your online application.

About CSL Vifor

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CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency and nephrology. We specialize in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL , headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries.

We want CSL to reflect the world around us

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL .

Do work that matters at CSL Vifor!

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