GlaxoSmithKline 1,067 reviews - Rockville, MD

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Basic qualifications:
  • 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.
Preferred qualifications:
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.
Contact information:
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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About this company
1,067 reviews
GlaxoSmithKline plc (GSK) is a global healthcare group, which is engaged in the creation and discovery, development, manufacture and...