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Synthetic Molecules Technical Development Specialist
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Company Overview
Roche is a leading research-focused healthcare group with over 100,000 employees across 100 countries. We strive to create innovative solutions that improve lives worldwide.
The Role
We are seeking a highly skilled GMP Compliance Specialist to join our Synthetic Molecules Technical Development team. As a key member, you will provide expertise and support in GMP compliance for IMP manufacturing and technical development.
Your Responsibilities:
- Facilitating GMP compliance processes for PTDC in collaboration with the global PQS network.
- Participating in global PQS document lifecycle processes and influencing authoring communities.
- Managing and tracking local impact assessments and implementation of current PQS requirements.
- Serving as an expert and first-level support for quality systems and their respective business processes.
- Optimizing and standardizing GMP-related processes and the existing document landscape.
Your Qualifications:
- A Master's degree or equivalent in chemistry, pharmaceutical sciences, or exceptional experience in a GMP environment within the pharmaceutical industry.
- Experience in synthetic molecule manufacturing and/or quality control is beneficial.
- Fluency in German and English, with excellent communication skills.
- An ability to collaborate effectively with diverse international teams.
