Take a key role in GMP-regulated pharmaceutical manufacturing environments and actively shape how modern medicines are produced. In this position, you will work close to production, quality and decision-makers, contributing directly to high-impact manufacturing setups across Fill & Finish operations. The role offers a strong mix of technical ownership, responsibility and influence within complex production landscapes.
Key responsibilities
* Drive technical activities across pharmaceutical production and Fill & Finish operations
* Develop and implement production concepts and layouts in compliance with cGMP
* Ensure smooth coordination between production, quality and technical stakeholders
* Take ownership of technical topics and decision-making
* Provide hands-on expertise on process and GMP-related challenges
* Support cost estimations and technical input for production initiatives
* Actively contribute to knowledge sharing and continuous improvement
Your profile
* Degree or technical training in pharmaceutical technology, process or mechanical engineering
* Several years of experience in GMP-regulated pharmaceutical manufacturing
* Mandatory hands-on experience in Fill & Finish (liquid and/or solid dosage forms)
* Strong understanding of drug product manufacturing processes
* Confident working with GMP standards and regulatory expectations
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