Project Director and Operations Head

Novartis Farmacéutica; Nürnberg; Vor Ort; EUR 100.000 - 125.000; Vollzeit

Zusammenfassung

Ein etabliertes Unternehmen sucht einen Projektleiter für eine hochmoderne Produktionsstätte im Bereich Radioligand-Therapien. Diese spannende Rolle umfasst die Verantwortung für die Einhaltung von Sicherheits- und Qualitätsstandards sowie die Führung eines engagierten Teams. Sie werden die strategische Planung leiten, um die Unternehmensziele zu erreichen und gleichzeitig die Effizienz und Compliance der Betriebsabläufe zu gewährleisten. Wenn Sie eine Leidenschaft für die pharmazeutische Industrie haben und in einem dynamischen Umfeld arbeiten möchten, ist dies die perfekte Gelegenheit für Sie.

Qualifikationen

• Mindestens 10 Jahre Erfahrung in der pharmazeutischen Industrie, davon 5 Jahre in Führungspositionen.
• Erfahrung als Projektleiter mit umfangreicher Projektmanagement-Hintergrund.

Aufgaben

• Leitung des Produktionsstandorts zur Erreichung von Sicherheits- und Qualitätszielen.
• Entwicklung und Kommunikation des strategischen Plans zur Erreichung der Unternehmensziele.

Kenntnisse

Strategisches Denken

Projektmanagement

Zusammenarbeit in Matrixorganisationen

Kommunikationsfähigkeiten

Kenntnis der cGMP-Vorschriften

Führungskompetenz

Ausbildung

Bachelor in Chemieingenieurwesen

Bachelor in Chemie

Bachelor in Pharmazie

Jobbeschreibung

The Project Director is responsible for leading a new state of the art manufacturing facility in achieving all objectives in key areas such as Safety, Supply, Cost, Quality, and People for a GMP Radioligand Therapies Production Site. The leader is responsible to translate Novartis Manufacturing and Supply and Country strategies into actionable action plans including preparation and execution of capital projects; constantly improve operational efficiencies at the site; ensuring the site has adequate resources and capabilities to ensure CGMP compliance, quality, service to patients, and people development.

About the Role

Possible locations: Halle, Dresden, Leipzig.

Major Accountabilities:

• Direct and manage Production, HSE (Safety), Engineering, Supply Chain and Manufacturing Science & Technology activities.
• Lead the site leadership team comprised of department heads from each function, monitoring team performance to company goals and objectives through use of established metrics, driving cross-site collaboration within their respective functions.
• Ensure the site, people, operations, and processes are compliant with cGMP, safety rules and other applicable regulations.
• Coordinate site activities through planning to ensure the overall manufacturing objectives are accomplished in a timely and cost-effective manner.
• Collaborate with other Site Heads to determine processes and procedures, which can be used across sites and where variances are needed to meet the unique needs of the site.
• Develop and communicate the site strategic plan to achieve company short-term and long-term objectives.
• Provide leadership to site employees including appropriate direction, mentoring and development opportunities. Maintain a positive work environment that supports positive team relations and teamwork.
• Plan and lead site meetings to ensure compliance with site policies, safety regulations, procedures, and processes. Also ensures compliance with company policies and provides a forum for questions and discussion about impact to the site of company initiatives.
• Investment projects and project management from construction to product launch.

Obligatory requirements:

• Bachelor's degree in chemical engineering, chemistry, pharmacy, or related field (or equivalent experience).
• Minimum 10 years of experience in the pharmaceutical industry, with at least 5 years in leadership roles, including experience with sterile manufacturing operations or relevant experience as site head or large scale PU.
• Experience as a Project Director / extensive project management background, especially in capital project execution.
• Strong strategic thinking with an enterprise focus.
• Excellent collaboration skills with experience working in a matrix organisation and solid communication skills.
• In-depth knowledge of cGMP regulations.
• Demonstrated ability to communicate effectively and inspire a large organization to achieve shared objectives.
• Fluent English and German, written and spoken.
• Experience with Health Authorities and inspections is highly desirable.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.