Dein Alltag dreht sich um die Planung und Umsetzung von Projekten für Marken. Du förderst die Kommunikation, erstellst umfassende Berichte und baust leistungsstarke Teams auf. Außerdem fungierst du als technischer Ansprechpartner für externe Partner und unterstützt die Evaluierung von Beschaffungsstrategien.
Anforderungen
- •Bachelor/Master degree in natural/life sciences
- •Project Management experience in pharmaceuticals
- •High flexibility and willingness to travel
- •Experience in sterile and aseptic CMC development
- •Knowledge of GMP requirements for CMC LCM activities
- •Experience in Drug Product manufacturing
- •Know-how in parenteral product primary packaging solutions
- •Effective multicultural work skills
- •Strong stakeholder engagement
- •Strong communication and negotiation skills
- •Analytical thinking and problem-solving skills
- •Adaptability to changing project requirements
- •Fluent in English, German is advantageous
Deine Aufgaben
- •Projekte für Marken planen und umsetzen
- •Effektive Kommunikation während der Projekte fördern
- •Umfassende Projektberichte erstellen und visualisieren
- •Hochleistungsfähige, funktionsübergreifende Teams aufbauen
- •Technischer Kontakt für externe Partner sein
- •Alternative Beschaffungsstrategien evaluieren und unterstützen
- •Sicherstellen, dass Beschaffungsstrategien übereinstimmen
- •Due-Diligence-Besuche bei potenziellen Auftragnehmern durchführen
- •Zu Vertragsherstellern reisen und Fortschritt überwachen
- •Hintergrundinformationen für Entscheidungsträger bereitstellen
- •Ziele und Vorgaben der Markenorganisation unterstützen
Original Beschreibung
# Technical Project Manager, CSL Vifor - Zurich
**EMEA, CH, Kanton Zurich, Opfikon, CSL Vifor** | **Full time**
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