Senior Manager Quality Systems (f/m/d) - global QMS Business Process Owner

TN Germany; Starnberg; Vor Ort; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

Ein etabliertes Unternehmen in der Pharmaindustrie sucht einen Senior Manager für Qualitätsmanagement, der eine Schlüsselrolle in der Verbesserung der globalen Qualitätssysteme spielt. In dieser spannenden Position leiten Sie ein Team von Qualitätsmanagern und fördern eine Kultur der kontinuierlichen Verbesserung. Sie sind verantwortlich für die Entwicklung und Implementierung von Qualitätsprozessen und arbeiten eng mit verschiedenen Stakeholdern zusammen, um sicherzustellen, dass alle Qualitätsstandards eingehalten werden. Wenn Sie eine Leidenschaft für Qualität und Führung haben und in einem dynamischen Umfeld arbeiten möchten, ist dies die perfekte Gelegenheit für Sie.

Qualifikationen

• Mindestens 10 Jahre Erfahrung im Qualitätsmanagement in der Pharmaindustrie.
• Erfahrung in der Führung von internationalen Teams und Matrixorganisationen.

Aufgaben

• Leitung eines Teams von Qualitätsmanagern und Unterstützung bei digitalen Initiativen.
• Definition und Standardisierung von Qualitätsprozessen im gQMS-Rahmen.

Kenntnisse

Qualitätsmanagement

Führungskompetenz

Regulatorische Kenntnisse

Analytische Fähigkeiten

Kommunikationsfähigkeiten

Verhandlungsgeschick

Ausbildung

PhD in Pharmazie

Master in Chemie

Master in Biologie

Tools

MS Office

eQMS

Jobbeschreibung

Senior Manager Quality Systems (f/m/d) - Global QMS Business Process Owner, Starnberg

Are you ready to make a meaningful contribution to patients' health and take on responsibilities in a dynamic environment? Join Aenova, a leading contract manufacturer and developer for the pharmaceutical industry, with 4,000 employees across 15 sites. Our headquarters in Starnberg, Germany, is seeking a Senior Manager Quality Systems.

Key Responsibilities

1. Lead and manage a team of Quality Managers overseeing their respective business process areas (documentation, training, eQMS, etc.) in collaboration with teams responsible for CSV, supplier qualification, audits, inspections, and regulatory surveillance.
2. Support the deployment of digitalization initiatives aligned with the overall Quality strategy and operational objectives.
3. Define and standardize Quality processes across the organization, ensuring site and department alignment within the gQMS framework.
4. Provide technical and regulatory guidance, develop training plans, and coach teams on gQMS deployment, promoting system usage.
5. Manage the creation and revision of global quality documents, including policies, SOPs, and guidelines, in collaboration with stakeholders.
6. Foster a holistic Quality culture promoting a collaborative environment for continuous improvement and the 'One Quality' mindset.

Your Profile

1. Minimum of 10 years of professional experience in Quality within the pharmaceutical, biotech, or medical device sectors, with senior management responsibilities (e.g., Department Head).
2. Advanced degree (e.g., PhD) in Pharmacy, Chemistry, Biology, or related fields such as IT or engineering.
3. Proven leadership skills, with experience in Quality System Management and implementation.
4. Ability to analyze, plan, and manage in a fast-paced, dynamic environment.
5. Experience working within a matrix organization, with strong negotiation, leadership, and communication skills to lead international teams.
6. Proficiency in MS Office and other information systems tools.
7. Excellent language skills; additional languages are a plus.

Your Motivation

If you seek new challenges in a competitive environment and prefer a solutions-oriented, proactive culture, we would love to discuss our corporate benefits with you. For inquiries, contact Melanie Rümmele, Human Resources.