- M.S. or PhD in Chemical engineering, Biochemistry, Biology, or related discipline with > 8 years of relevant experience in pharmaceutical or biologics process development.
- Strong technical knowledge and proven experience in protein or monoclonal antibody downstream process development.
- Must have excellent verbal and written communication skills and be able to work effectively in a team and independently under general supervision.
Prior experience in process characterization and/or process validation is highly desirable.
- Prior experience with cGMP and/or pilot scale production is a plus.
- Prior experience with use of statistical tools such as JMP software or equivalent is highly desirable
- Develop, optimize and scale up downstream process involving chromatography and filtration steps for the production of clinical and commercial supplies.
- Design and execute scale-down experiments for trouble shooting of development and manufacturing problems.
- Involvement in design experiments (DOE) leading to process characterization and validation.
- Support product scale-up and technology transfer to manufacturing facilities
- Prepare technical reports and protocols.
- Present data at relevant forums across multiple levels of the organization.
- Maintain accurate laboratory notebooks and relevant documentation.
You may apply for this position online by selecting the Apply now button.
GlaxoSmithKline is an equal opportunity employer, M/F/D/V - and we are proudly committed to diversity in our workforce.
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GlaxoSmithKline - 17 months ago
GlaxoSmithKline plc (GSK) is a global healthcare group, which is engaged in the creation and discovery, development, manufacture and...