GMP Quality Control Specialist II

Novartis AG; Tirol; Sur place; EUR 61 000 - 96 000; Plein temps

Avantages offerts par ce poste

Modern company pension scheme

Childcare facilities

Learning and development opportunities

Worldwide career possibilities

Résumé du poste

Novartis AG in Austria seeks a quality-focused professional to oversee production and testing, ensuring GMP and quality standards across records and releases. You will investigate deviations, approve data, and support audits within QC, contributing to lifecycle documentation and site-wide improvements.

The role requires life sciences expertise, QA experience, and fluency in German and English, with hybrid opportunities and a market-aware compensation package.

Qualifications

• Degree in life sciences or related field.
• Experience in pharmaceutical quality control or quality assurance.
• Good Manufacturing Practice knowledge and regulated quality standards.
• Experience with environmental monitoring and controlled cleanliness zones.

Responsabilités

• Oversee production and testing activities, ensuring GMP & quality standards.
• Review and approve production, quality control and analytical records.
• Evaluate deviations and corrective actions, change requests.
• Support investigations into exceptions, identify risks and resolutions.
• Approve QC and release data, ensuring accuracy and data integrity.
• Prepare for and support audits within QC area.
• Maintain lifecycle documentation per quality requirements.
• Contribute to continuous improvement projects across the site.

Connaissances

GMP knowledge

Quality assurance

German & English

Cross-functional collaboration

Digital skills

Formation

Life sciences degree

Outils

Quality information systems

Description du poste

Novartis AG in Austria seeks a quality-focused professional to oversee production and testing, ensuring GMP and quality standards across records and releases. You will investigate deviations, approve data, and support audits within QC, contributing to lifecycle documentation and site-wide improvements.

The role requires life sciences expertise, QA experience, and fluency in German and English, with hybrid opportunities and a market-aware compensation package.