Process Expert (m/f/d) - Halle (saale), Sachsen-anhalt
Stellen Nordrhein Westfalen
Halle (Saale), Germany
Hybrid
Gmp manufacturing experience
Process understanding
Quality issues awareness
The job posting is for a Process Expert at Novartis in Halle (Saale), Germany, focusing on providing front-line manufacturing support, ensuring compliance with quality requirements, and leading investigations into process issues. The ideal candidate should possess a relevant degree, at least three years of experience in GMP manufacturing, and strong technical writing skills in both German and English
Job Summary
As a Process Expert, you will provide front-line support to manufacturing, ensuring batches are manufactured safely and in compliance with instructions and quality requirements.
You will act as the Subject Matter Expert (SME) for product and process knowledge, driving investigations to root cause and implementing corrective actions.
Key responsibilities include managing manufacturing documentation, authoring investigations, supporting process optimization, and providing guidance to the production team through training and knowledge sharing.
Matching Summary
Match Score: 85
The job posting is for a Process Expert at Novartis in Halle (Saale), Germany, focusing on providing front-line manufacturing support, ensuring compliance with quality requirements, and leading investigations into process issues. The ideal candidate should possess a relevant degree, at least three years of experience in GMP manufacturing, and strong technical writing skills in both German and English.
Skills & Requirements
Must-have
GMP manufacturing experience
Process understanding
Quality issues awareness
Compliance investigations
Technical writing skills
Fluent in German and English
Nice-to-have
Radio pharma experience
Leadership experience
Cross-functional experience
Data Analytics
digital skills
General Hse Knowledge
process excellence
Resilience
Key Requirements
Bachelor’s degree in engineering, Pharmacy, Pharmaceutical Technology, Chemistry or relevant experience
3 years’ experience in GMP manufacturing or QA/QC
Proven process understanding (Pharma, GMP, Regulatory aspects)