Du harmonisierst globale CSV-Prozesse, leitest Projekte aus der Qualitätsvalidierungs-Perspektive und schult das Team zur Verbesserung der technischen Expertise.
Anforderungen
- •Bachelor’s degree in life science or engineering
- •Over 10 years of experience in international quality engineering
- •More than a decade of expertise in medical devices
- •Deep understanding of leading QM processes and tools
- •Proven leadership abilities in strategic quality initiatives
- •Autonomy and proactive approach
- •Exposure to global companies and diverse cultures is advantageous
- •Proficient in English; additional languages are a plus
Deine Aufgaben
- •Globale CSV-Prozesse harmonisieren und optimieren
- •Globale CSV-Projekte aus der Qualitätsvalidierungs-Perspektive leiten
- •CSV-Teammitglieder schulen und weiterentwickeln
- •Cross-funktionale Projekte managen und mit Stakeholdern zusammenarbeiten
- •CSV-Dokumentation überprüfen und genehmigen
- •Risikomanagement in CSV-Projekten proaktiv vorantreiben
Deine Vorteile
Rolle im globalen QM-Umfeld
Viele soziale Vorteile
Jährliches Mindestgehalt in Österreich
Original Beschreibung
# Head of Computerized System Validation (CSV) (all genders)
Location:
Kremsmünster, AT, 4550
Monroe, US, 28110
Frickenhausen, DE, 72636
Travel activity:
10%
Job Type:
Permanent
## Your Challenge
We are looking for a skilled and driven leader to join our global quality team. As the Head of Computerized System Validation (CSV), you will lead and harmonize global CSV processes, ensuring their effectiveness and compliance. Your role will focus on driving validation activities, optimizing processes, and fostering collaboration across the organization.
**Your main responsibilities will include:**
* Harmonize and optimize the global CSV process, ensuring compliance and effectiveness.
* Lead global CSV projects from a Quality Validation perspective.
* Train and upskill CSV team members to maintain and improve technical expertise.
* Manage cross-functional projects and collaborate with key stakeholders.
* Review and approve CSV documentation to ensure regulatory compliance.
* Drive risk analysis in CSV projects, ensuring proactive risk management.
## Your profile
* Hold a Bachelor’s degree in a relevant life science or engineering discipline.
* Bring over 10 years of experience in international quality engineering with a focus on CSV.
* Have more than a decade of expertise in the medical device sector.
* Possess a deep understanding of leading QM processes and tools.
* Demonstrate proven leadership abilities in managing strategic quality initiatives.
* Showcase autonomy and a proactive approach to your work.
* Previous exposure to global companies and diverse cultures is advantageous.
* Be proficient in English; additional languages are considered a plus.
* Office location: any GBO site.
## Our Offer
We offer you a role in a global QM environment with the opportunity to further develop your existing qualifications. In addition to our many attractive social benefits, the minimum annual salary in Austria is based on employment group IV of the collective agreement for the chemical industry. In other countries, compensation may vary based on local market conditions and legal frameworks.
We provide equal opportunities for everyone and see diversity as our strength. Therefore, we welcome all applicants – regardless of characteristics such as gender, age, background, social status, sexual orientation, religion, or mental and physical abilities. We have set the goal of empowering women and increasing female leader representation. We foster an inclusive work environment and encourage all individuals to apply.
Job ID:
2686