Your Key Responsibilities: Plan and design new, especially modular production systems for the continuous manufacturing of drug substance intermediatesAnalyze and assess technologies and systems to ensure GMP complianceDefine qualification strategies and ensure GMP-compliant implementation in collaboration with Quality AssuranceCreate technical specifications (URS) and work closely with suppliers and external partnersCoordinate technical risk analyses and contribute to safe plant operationsProvide technical expertise in investment projects – ensuring timelines, budgets, and quality targets are metBuild, consolidate and provide process-related knowledge globally across the organizationYour Profile:
Master's degree or PhD in Chemical Engineering, Process Engineering, Pharmaceutical Engineering, or a related field3–5 years of relevant experience in the pharmaceutical or chemical industry, ideally in GMP-regulated drug substance productionStrong analytical and problem-solving skills combined with a self-driven and solution-oriented mindsetExcellent communication and team collaboration skills
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