You assist in managing master data and ensuring quality assurance for raw materials and consumables, maintaining compliance and supporting troubleshooting efforts across various projects and systems.
Anforderungen
- •QC/QA in pharmaceutical industry
- •Experience with GMP procedures
- •Technological expertise and intelligence
- •Dealing with ambiguity
- •Ability to learn continuously
- •Collaborating across boundaries
- •English and German language required
Deine Aufgaben
- •Support CP implementation in SAP and master data systems.
- •Assist with QA master data topics for raw materials and consumables.
- •Create master data sheets and collect information.
- •Participate in projects and troubleshoot master data issues.
- •Address master data non-conformities related to raw materials.
- •Evaluate changes and provide PEM support for master data.
- •Assist in creating and collecting CoA for raw materials.
- •Support stability studies and master data maintenance.
- •Troubleshoot master data issues with connected units.
Deine Vorteile
Market-competitive base salary
Attractive incentive program
Modern company pension scheme
Childcare facilities
Learning and development opportunities
Worldwide career possibilities
Original Beschreibung
# QA Specialist Operations
**Kundl** | **Full time**
**Job Description Summary**
Manages Quality aspects and projects within area of responsibility. Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.
**Job Description**
**Major accountabilities:**
* CP implementation support in SAP and other master data systems
* Support QA master data related topics with regards to raw material and consumables
* Master data sheet creation and information collection; project involvement and troubleshooting (special focus on raw material and consumables topics around master data)
* Support of master data related non-conformities (DEV, QEs, complaints) affiliated to raw materials and consumables; change evaluations, PEM support in regard to master data related topics (focus on raw materials and consumables)
* CoA creation and collection support (focus on raw materials and consumables); support of stability studies; support of master data maintenance; support master data associated troubleshooting with connected units (sampling & printer issues etc.)
**Minimum Requirements:**
* QC/ QA in pharmaceutical ind./ biotech with environmental monitoring
* Experience with GMP Procedures, Quality Assurance (QA) and Quality Control (QC) testing, Quality standards
* Technological Expertise and technological Intelligence
* Required skills: Dealing with ambiguity, able to learn continuously, collaborating across boundaries
* English and German language required
**Skills Desired**
Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence