Junior Process Expert - GMP Manufacturing, Hybrid Work

Novartis Farmacéutica; Stein; Vor Ort; CHF 74.000 - 138.000; Vollzeit

Benefits dieser Stelle

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Flexible and hybrid working options

14 weeks of paid parental leave

Zusammenfassung

Novartis is seeking a Junior Process Expert at our Stein site. The role focuses on supporting the Production Unit in improving processes, both qualitatively and quantitatively, while complying with cGMP and SOP guidelines.

Major responsibilities include handling deviations and CAPAs, assisting in manufacturing instructions, quality notifications, and SOP development. The position requires a Master’s degree in a scientific discipline, GMP experience, and fluent English and German.

Qualifikationen

• Fluent in English and German.
• Degree in scientific disciplines.
• Master's degree.
• Initial GMP manufacturing experience.
• Proficient with Microsoft Office applications.
• Ability to work independently.

Aufgaben

• Supports deviations, complaints, actions, and CAPAs.
• Supports decision-making related to production issues.
• Assists in creating and maintaining manufacturing instructions, including bills of materials, process sub-steps, and process steps.
• Supports processing of quality notifications, including external and internal complaints.
• Assists in developing specific SOPs.
• Ensures adherence to GSU guidelines.
• Ensures cleanliness, hygiene, and order in the workplace.
• Assists in implementing corrective measures for deviations.
• Supports process and cleaning validations and assists with qualification activities.

Kenntnisse

Fluent English & German

Independent work

Ausbildung

Master's Degree

Degree in Scientific disciplines

Tools

Microsoft Office

Jobbeschreibung

Novartis is seeking a Junior Process Expert at our Stein site. The role focuses on supporting the Production Unit in improving processes, both qualitatively and quantitatively, while complying with cGMP and SOP guidelines.

Major responsibilities include handling deviations and CAPAs, assisting in manufacturing instructions, quality notifications, and SOP development. The position requires a Master’s degree in a scientific discipline, GMP experience, and fluent English and German.