Product Development Manufacturing Expert
Vor 3 Tagen
We are seeking a highly skilled Product Development Manufacturing Expert to lead our external manufacturing operations for drug products. This role will be responsible for providing process engineering support for all DP manufacturing conducted on behalf of CSL Behring Operations at contract manufacturing organizations (CMOs).
The ideal candidate will have significant international experience in aseptic/sterile processing and visual inspection of biopharmaceuticals, as well as excellent problem-solving skills and the ability to work effectively with cross-functional teams.
- Lead transition of technical oversight from project (tech transfer) to operations phases for DP external manufacturing
- Ensure key parameters for process monitoring are identified and charts (e.g. time series, control charts) are set up and maintained
- Ensure key process and asset attributes relevant to reducing variability are tracked, increasing performance of the process and visualizing in reporting
- Evaluate long-term trends, maintain log of loss drivers (e.g. performance, availability and quality losses), identify improvement levers, and plan robustness and continuous improvement initiatives
- Support deviations linked to process robustness, train and coach others on how to interpret robustness trends, actively liaise with other functions to identify loss drivers, including aseptic process/technology owner, QA specialist and broader Global Engineering
- Participate in cross-functional, external plant operations teams, act as single point of contact (SPOC) for Engineering in such teams, engage broader organization to drive problem solving capability and lead investigations through the use of problem-solving tools
- Provide technical person in plant (PIP) support for routine CMO operations as required and in conjunction with Quality PIP. Represent CSL Behring at technical interface with CMO partners
- University degree in engineering or science; higher degree preferred
- Aseptic/sterile processing and visual inspection of biopharmaceuticals in one or more of Operations, Process Engineering or Quality Assurance (5+ years post graduate experience)
- Fluency in German and English
- Experience in GMP, problem solving, continuous improvement, vendor relationships, data analysis & interpretation
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