Senior Scientist, Technical Project Lead

Key Responsibilities

• Lead end-to-end technical projects across technology transfers product lifecycle management and continuous improvement initiatives for assigned products and external manufacturing partners.
• Develop and execute robust Project Execution Plans by translating technical implementation strategies into actionable project plans with clear milestones timelines resource requirements and deliverables.
• Lead cross-functional project teams consisting of technical experts from multiple disciplines and external manufacturing partners to ensure successful project execution.
• Support project governance by proactively managing timelines budgets risks issues dependencies KPIs and project reporting.
• Prepare governance documentation business cases decision papers and escalation packages to support timely and effective decision-making.
• Act as the primary technical interface towards Contract Manufacturing Organizations (CMOs) and external partners throughout project execution.
• Foster strong collaboration through proactive stakeholder engagement effective communication and alignment across internal functions and external partners.
• Support technical due diligence activities manufacturing site assessments and the evaluation of alternative manufacturing and sourcing strategies for APIs drug products starting materials and raw materials.
• Provide on-site support at manufacturing facilities during key project phases to monitor progress facilitate implementation and resolve technical challenges.

Skills & Experience

Minimum Requirements

• Bachelors or Masters degree (or equivalent) in Life Sciences Pharmacy Chemistry Chemical Engineering Biotechnology Pharmaceutical Sciences or a related discipline.
• Demonstrated experience leading technical projects within the pharmaceutical biotechnology chemical or related industry.
• Experience in leading technology transfers product/process transfers lifecycle management and/or continuous improvement initiatives.
• Strong project management capabilities with the ability to independently lead complex cross-functional projects from initiation through completion.
• Self-driven proactive and able to take ownership in a dynamic environment.
• Excellent collaboration communication and stakeholder management skills.
• Experience working with external manufacturing organizations (CMOs/CDMOs).
• Willingness to travel internationally as required.

Preferred Requirements

• Solid understanding of GMP requirements and CMC lifecycle management
• Technical Background in CMC Development Technical Transfer Process Development Manufacturing Science or Commercial Manufacturing.
• Strong analytical thinking problem-solving and decision-making capabilities.
• Demonstrated ability to influence stakeholders and navigate complex matrix organizations.
• Experience working in an international multicultural environment.
• Fluent in English; German is considered an advantage.

CSL Vifor is a global partner of choice for pharmaceuticals and innovative leading therapies in irondeficiency 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 companyCSL headquartered in Melbourne Australia employs 32000 people and delivers its lifesaving therapies to people in more than 100 countries.

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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.

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