- Subject matter expert (SME) in sterile manufacturing processes
- Support the process capability analysis and Continuous Process Verification of key quality attributes and parameters at the different CMOs
- Provide Impact assessments of change requests
- Manage manufacturing or complaint investigations on product impact, including root cause analysis, CAPA generation, and impact assessment
- Able to work within and lead cross-functional technical teams, across multiple cultures
- Experienced in deviation investigator and GMP change management in sterile commerical production of drug product
- scientific or engineering degree
- 2-4 y experience in commercial manufacturing of sterile drug products
- Experience in parenteral compounding and filling
- Involvement in deviations, CAPA's and risk assessmets (FMEA)
- Understanding of process, engineering, analytical and regulatory aspects of sterile drug product manufacturing
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Parenterals Tech Transfer Manager - Yverdon-les-Bains, Schweiz - gloor&lang AG
Beschreibung
Corporate Role MS&T CMO Management
Our customer is a major player in the biopharmaceutical industry, offering a wide range of globally established and recognized products. The new position of a Manager for Sterile Drug Product requires significant experience in manufacturing, compounding and filling of sterile drug products in vials, pre-filled syringes and cartridges.
Support the young team of Global External Manufacturing in this challenging corporate role
Your expertise:
You have in depth technical knowledge of sterile manufacturing technology and processing techniques.
Your abilities:
You identify and execute process robustness improvement projects, where required. Using this information and knowledge to contribute to comprehensive and accurate annual product reviews, as well as performance assessment of CMOs.
Your skill profile:
Your solution-oriented approach allows you to communicate and negotiate in an effective way. Your English is fluent. The position requires occasional level of travel.