Tax Manager natürliche Personen 80%-100%

Deloris AG; Zürich; Vor Ort; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

An established industry player in pharmaceuticals is looking for a Technical Project Manager to join their dynamic team in Zurich. This hybrid role involves planning and executing critical projects related to CMC Development and Technology Transfer. You will lead cross-functional teams, ensure project deliverables are met, and facilitate effective communication with stakeholders. The position offers significant opportunities for professional growth and requires a strong background in project management within the pharmaceutical sector. If you are adaptable, have excellent communication skills, and are ready to make an impact, this is the perfect opportunity for you.

Qualifikationen

• Qualification in natural/life sciences or associated engineering degree.
• Experience in Project Management in the pharmaceutical industry.

Aufgaben

• Plan and monitor projects for allocated brands, ensuring deliverables are met.
• Build and manage cross-functional teams for project implementation.
• Prepare project reports and define KPIs for stakeholders.

Kenntnisse

Project Management

Communication Skills

Analytical Thinking

Problem-Solving Skills

Stakeholder Engagement

Flexibility and Willingness to Travel

Ausbildung

Bachelor in Natural Sciences

Master in Life Sciences

Jobbeschreibung

We are seeking 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 diverse responsibilities and opportunities for professional growth.

Key Responsibilities

1. Plan, implement, drive, and monitor projects for allocated brands / CMOs, ensuring deliverables, timelines, and budgets are met.
2. Facilitate effective communication throughout projects by proactively engaging in periodic calls and meetings.
3. Prepare comprehensive project reports, including plans, status updates, presentations, and meeting minutes, while defining and visualizing relevant KPIs.
4. Build and manage high-performing, cross-functional teams, implementing complex projects and initiatives at external and internal manufacturing sites.
5. Serve as the key technical interface for external partners and contract manufacturing organizations on allocated projects / brands.
6. Support and drive the evaluation of alternative, cost-effective sourcing strategies for API, DP, starting and raw materials by coordinating technical development work and vendor evaluation.
7. Ensure proposed and established sourcing strategies align with corporate and brand strategies as set forth by governing bodies.
8. Conduct due diligence visits at potential future contract manufacturing organizations.
9. Travel to contract manufacturers to monitor project progress, support implementation, and troubleshoot as needed.
10. Provide background information, documentation, and technical advice to decision bodies and negotiation teams to facilitate timely decisions.
11. Support the achievement of goals and targets for the respective brand organization.

Skills & Experience

• Qualification in natural / life sciences or associated engineering degree (e.g., Biology, Biochemistry, Chemistry, Pharmaceutics), Bachelor / Master level or equivalent.
• Experience in Project Management and Delivery in the 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 to CMC LCM activities.
• Experience in Drug Product and Finished Product manufacturing & Technology Transfer.
• Knowledge of 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 skills.
• Excellent communication and negotiation skills.
• Analytical thinking & problem-solving skills.
• Ability to adapt to changing project requirements.

Languages: Fluent English; German is an advantage.

This is a hybrid role based in Zurich, Switzerland.

Application deadline: 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 worldwide with severe, chronic, and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing, development, manufacturing, and marketing of pharmaceutical products for precision patient care.

For more information, please visit viforpharma.com.

We want CSL to reflect the world around us

As a global organization with employees in over 35 countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.