Junior GMP Process Specialist — Continuous Improvement

Novartis

Stein

Vor Ort

CHF 74.000 - 138.000

Vollzeit

Vor 12 Tagen
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Benefits dieser Stelle

Insurance plans
Retirement plans
Wellbeing resources
Global recognition programs
Flexible and hybrid working options
14 weeks paid parental leave

Zusammenfassung

Novartis in Stein is seeking a Junior Process Expert to support the Production Unit in improving processes and implementing new ones. The role requires adherence to cGMP, SOPs and guidelines, with emphasis on deviations, CAPAs, and manufacturing instructions.

The candidate should have a scientific degree, strong independence, MS Office skills, and fluency in English and German. A 12-month temporary contract is offered with flexible/hybrid benefits where applicable.

Qualifikationen

  • Bachelor-level or higher degree in scientific disciplines.
  • Ability to work independently.
  • Proficiency in Microsoft Office applications.
  • Fluent English and German.

Aufgaben

  • Supports the handling of deviations, complaints, actions, and CAPAs.
  • Provides support in decision‑making related to production issues.
  • Assists in the creation and maintenance of manufacturing instructions, including bills of materials, process sub‑steps, and process steps.
  • Supports the processing of quality notifications, including external and internal complaints.
  • Assists in the development of specific SOPs.
  • Ensures GMP‑compliant documentation.
  • Consistently adheres to GSU guidelines.
  • Ensures cleanliness, hygiene, and order within the work environment.
  • Assists in implementing corrective measures for deviations.
  • Supports process and cleaning validations and assists with qualification activities (e.g., thermal requalification).

Kenntnisse

MS Office
Independent work
English
German

Ausbildung

Degree in Scientific disciplines
Master's Degree

Jobbeschreibung

Novartis in Stein is seeking a Junior Process Expert to support the Production Unit in improving processes and implementing new ones. The role requires adherence to cGMP, SOPs and guidelines, with emphasis on deviations, CAPAs, and manufacturing instructions.

The candidate should have a scientific degree, strong independence, MS Office skills, and fluency in English and German. A 12-month temporary contract is offered with flexible/hybrid benefits where applicable.

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