QA Mgr Computerized System Validation

Job description

Stellenbeschreibung

Ensure that all aspects of Computerized Systems Validation (CSV) comply with GxP and Novartis requirements throughout the life cycle of systems

Facilitate implementation of global initiatives related to CSV and data management

QA contact between IT, business functions and other QA departments for quality related topics regarding CSV

Provide guidance to internal stakeholders within the CSV framework

Support regulatory inspections and responses to observations, including preparatory activities related to CSV for upcoming inspections
Positionsbezeichnung

QA Mgr Computerized System Validation

Desired profile

Mindestanforderungen

University degree in natural / technical sciences or equivalent education

Fluency in English, fluency in German not required but of advantage

Min. 3 years of experience in pharmaceutical industry related to e-compliance / CSV

- Conceptual / analytical thinking
- Good and open interpersonal communication skills
- Solution oriented work style
- Focus on implementation of assigned tasks

We offer a market-competitive base salary in line with your qualification, experience and individual competencies. Additionally we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning & development options and worldwide career opportunities within the Novartis group. The base pay is composed of a market oriented excess payment and the respective amount according to the Austrian collective agreement (at least € 54000,- per year)
Art der Stelle

Vollzeit
Land

Österreich
Standort

Kundl
Funktionsbereich

Quality
Division

Novartis Technical Operations
Geschäftseinheit

NTO QUALITY
Anstellungsverhältnis

Unbefristet
Unternehmen/Rechtsträger

Sandoz GmbH