Job ID REQ-10068587
Verantwortlich für das Management von Qualitätsaspekten innerhalb des Verantwortungsbereichs und um sicherzustellen, dass das operative Geschäft in Übereinstimmung mit cGMP (Current Good Manufacturing Practices), der Qualitätssicherungsvereinbarung, den regulatorischen Anforderungen und dem Novartis Qualitätshandbuch erfolgt und nach den entsprechenden Standardarbeitsanweisungen durchgeführt wird  About the RoleKey Responsibilities:

* Oversight of GxP functions across site and ensure product quality. Implement, comply with, and govern practices prescribed in the Novartis Manufacturing Manual
* Act as release responsible person; ensure regulatory compliance and implementation of corporate quality standards and regulations. Ensure status of local HA registration and qualified state of facilities and utilities
* Review and approval of PQR / APQR; ensure exception (deviation and OOX) and complaint management and investigation as well as proper definition and implementation of CAPAs
* Ensure DI, eCompliance and compliance with all cGxP and all regulatory requirements for manufacturing, control and distribution operations; ensure adherence to HSE guidelines and requirements
* Collaboration in internal and external audits; ensure any collaborations with 3rd parties are performed with adequate Quality Assurance Agreements in place
* MBR review and approval; approval of specifications, sampling instructions, test methods and other quality control procedures
* Participation in the compilation, revision and approval of validations, transfers, SOPs and other GxP related documents as applicable
* Support transfer projects & validation studies; Author of SOPs and other GxP documents as applicable





Essential Requirements:

* University Degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology or equivalent
* Professional experience in pharmaceutical industry, with direct experience with Pharmaceuticals, Biopharmaceutical or API products and at least 2 years within QA
* Thorough knowledge of cGMP requirements as well as proven track record with FDA / EMA and other Health Authorities
* Knowledge of GMP and Management of Quality Audits
* Flexibility to work in a fast paced, quickly changing work environment
* Knowledge of Manufacturing Process/ Product Expertise
* Fluent knowledge of English and German (written and spoken)





You'll receive:
In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 65.605,54 year (on a full-time basis). In most cases, the actual salary will be higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies.
We are open for part-time and job-sharing models and support flexible and remote working where possible. For this position we are not offering relocation package.



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


Wir freuen uns über Ihre vollständigen und aussagekräftigen Bewerbungsunterlagen über das BrassRing Novartis Recruiting System unter https://www.novartis.com/careers (Job ID siehe oben )

https://www.novartis.com/careers/career-search/job/details/req-10068587-qa-operations-expert-dmf-de-de