* Coordinate and ensure the preparation and maintenance of documentation (e.g., SOP / WI, protocols / reports) within your area of expertise.
* Support the scaling-up from 200L to 2000L of suitable purification processes for manufacturing operations (Pre-clinical and Clinical).
* Assist your manager in coordinating activities within your scope of responsibility.
* Produce large-scale NBEs for pre-clinical or clinical studies.
* Provide small-scale production and laboratory services.
* Maintain a close relationship with the local Engineering and Technology organization as needed.
* Support the implementation of roadmap strategies and / or global initiatives.
* Act as a Subject Matter Expert during audits related to large-scale manufacturing and technology transfer activities.
Your Profile
* Master's degree in science or engineering, or a technical diploma with a minimum of 5 years of experience
* Ensure quality by designing robust operations and conducting regular quality checks
* Collaborate with stakeholders to optimize products or services through new technologies
* Work with agility by flexibly assigning resources to adapt to changing business needs
* Be efficient by removing barriers and taking responsibility for outputs
* Present ideas clearly and assertively
* Ensure timely delivery of results in line with project plans
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