QC Specialist II — Pharma Quality & Compliance

AT33 (FCRS = AT033) Novartis Pharmaceutical Manufacturing GmbH; Österreich; On-site; EUR 54,000 - 66,000; Full time

Benefits offered by this job

Incentive program

Company pension

Childcare facilities

Learning & development opportunities

Global career possibilities

Job summary

AT33 (FCRS = AT033) Novartis Pharmaceutical Manufacturing GmbH in Schaftenau, Austria, seeks a QC Specialist II for a 2-year contract. You will manage analytical equipment, ensure GMP compliance, and support continuous improvement. Fluency in German and English is required, with a strong quality control background.

The role emphasizes collaboration across teams, documentation accuracy, and regulatory readiness to ensure each batch meets the highest standards before reaching patients worldwide.

Qualifications

• University degree in natural sciences or relevant vocational training.
• Three to five years of experience in a pharmaceutical or manufacturing quality environment.
• Experience in a Good Manufacturing Practice regulated laboratory.
• Strong knowledge of quality control processes and compliance.

Responsibilities

• Manage analytical equipment lifecycle while ensuring compliance.
• Execute laboratory activities and documentation per GMP standards.
• Review, compile, and approve quality records and technical documentation.
• Maintain and improve SOPs, analytical methods, and lab processes.
• Investigate deviations and support timely resolution.
• Coordinate quality control activities with internal teams and external labs.
• Support inspections, audits, change controls, and continuous improvement initiatives.

Skills

Quality control

German language

English language

Education

University degree in natural sciences

Job description

AT33 (FCRS = AT033) Novartis Pharmaceutical Manufacturing GmbH in Schaftenau, Austria, seeks a QC Specialist II for a 2-year contract. You will manage analytical equipment, ensure GMP compliance, and support continuous improvement. Fluency in German and English is required, with a strong quality control background.

The role emphasizes collaboration across teams, documentation accuracy, and regulatory readiness to ensure each batch meets the highest standards before reaching patients worldwide.