Jr. Process Expert Cgt
vor 2 Wochen
385593BR
**Jr. Process Expert CGT (temp)**:
Switzerland
**About the role**
**Process Expert CGT (temp), Stein, Switzerland**
**43 million** the total no of patients we reached in 2022 through our collective efforts to reimagine medicine and make a real difference to the lives of patients around the world.
As a Jr Process Expert you will support PU by providing front line expert support for all process-specific issues to ensure execution of processes on time, continuously improving in quality and productivity, performed in compliance to cGMP, SOPs and applicable guidelines and functional standards.
**Your key responsibilities**:
Your responsibilities include, but are not limited to:
- Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements.
- Responsible for maintaining the master manufacturing documents of assigned products (e.g. Master Batch Record, Bill of Material (BOM) & Recipe, Quality Risk Assessment, Zurich Hazard Analysis).
- Ensure that all critical parameters are within written Instruction (i.e. Master Batch Record).
- Support steward for assessment of technical changes and process changes (task manager ACC/PCC).
- Ensure that all process changes are managed through appropriate change control procedure.
- Execute process improvements and scale-up.
- Ensure that technical batches generate sufficient process knowledge by thoroughly testing critical variables.
- Support technology trainings and education programs for production operators.
- Act as Subject Matter Expert for Audits.
We offer a temporary position with a max. 2 year duration.
**Commitment to Diversity & Inclusion**:
- We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._
**Role Requirements**
**What you’ll bring to the role**:
- Desirable BSc. in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy with further qualifications in Production Management or equivalent.
- Fluent in English/proficiency in German.
- Desirable: previous experience in process support role on the shop floor of GMP manufacturing and/or QA/QC.
**Why Novartis?**
**You will receive**:
**Division**
Operations
**Business Unit**
CELL & GENE THERAPY
**Work Location**
Stein (Säckingen)
**Company/Legal Entity**
Novartis Pharma AG
**Functional Area**
Technical Operations
**Job Type**
Full Time
**Employment Type**
Temporary
**Shift Work**
Yes
**Early Talent**
No
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