GMP Process Improvement Associate

Novartis; Stein (AR); Hybrid; CHF 74.000 - 138.000; Vollzeit

Benefits dieser Stelle

Hybrid work options

Parental leave

Zusammenfassung

Novartis in Stein (AR) is seeking a Junior Process Expert to support the Production Unit in improving existing processes and introducing new ones, in line with cGMP and SOPs. The role focuses on deviations, CAPAs, and manufacturing instructions, ensuring compliant documentation and clean, orderly work environments.

Fluent in English and German, you will work independently in a GMP setting, contributing to quality improvements and process validations.

Qualifikationen

• Degree in Scientific disciplines is required.
• Ability to work independently.
• Proficiency in Microsoft Office applications.
• Fluent in English and German.

Aufgaben

• Supports handling of deviations, complaints, actions, and CAPAs.
• Provides support in decision-making related to production issues.
• Assists in creating and maintaining manufacturing instructions, BOMs, process sub-steps, and process steps.
• Supports processing of quality notifications, including external and internal complaints.
• Assists in development of specific SOPs.
• Ensures GMP-compliant documentation.
• Maintains cleanliness, hygiene, and order in the work area.
• Assists in implementing corrective measures for deviations.
• Supports process and cleaning validations and qualification activities.

Kenntnisse

Data Analytics

Independent work

MS Office

Fluent English

Fluent German

Ausbildung

Degree in Scientific disciplines

Master’s Degree

Tools

Microsoft Office

Jobbeschreibung

Novartis in Stein (AR) is seeking a Junior Process Expert to support the Production Unit in improving existing processes and introducing new ones, in line with cGMP and SOPs. The role focuses on deviations, CAPAs, and manufacturing instructions, ensuring compliant documentation and clean, orderly work environments.

Fluent in English and German, you will work independently in a GMP setting, contributing to quality improvements and process validations.