Senior Scientist, Drug Substance and Product Analysis

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Job description

We are building a state-of-the-art end to end Biopharm capability which delivers efficient discovery of antibody molecules that are selected and engineered for rapid development so that, together with our therapy area partners, we discover, develop and manufacture novel portfolio of exciting medicines to benefit patients around the world. If you aim to be part of a global cutting edge drug development and discovery organization and are motivated to contribute towards bringing lifesaving drugs to patients, join us!

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#GSKBiopharm_Development

Are you looking for a collaborative analytical chemist role that allows you to contribute to scientific strategy and accelerate Pharmaceutical Research and Development? If so, this role could be an ideal opportunity to explore.

GlaxoSmithKline (GSK) is a world leading research-based pharmaceutical company that combines both individual talent and technical resources to create a platform for the delivery of strong growth in a rapidly changing healthcare market. Our mission is to improve the quality of human life by enabling people to do more, feel better, and live longer.

Product Development and Supply is a highly experienced Chemistry, Manufacturing and Controls (CMC) organization accountable for delivering robust, cost effective and competitive products and manufacturing processes spanning the fulllife-cycleof asset development from Discovery through commercialization. These activities are delivered through state-of-the-art internal facilities as well as strategic external partners. Collectively, the team is accountable for CMC activities encompassing cell line development, cell culture/ microbial fermentation, purification development, and drug product/ device development. We also pioneer innovative technologies to improve robustness, reduce cost of goods, and improve the patient experience.

AsanSenior Scientist, you will design and performexperiments thatdevelop, qualify, and implementvarious analytical methods and state-of-the art analytical technologies that focus on product quality and/or process-specific analytes and support various aspects of biopharmaceutical process development and manufacturing. You will be involved in all aspects of the biopharmaceutical development, including engagement with project teams and other stakeholders for various projects in different stages of development.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Develop andperformassays thatsupport thedevelopment,release and stability testing ofBiopharmaceuticaldrug substance and drug product.
• Review of experiments, stability protocols, and other key documents
• Influence the direction of associatedanalytical control strategies across the biopharm process.

• Contribute and support departmental cross-training activities on analytical techniques used for analysis of biopharm molecules.
• Contribute tosections for patents or regulatory submissions, as well asscientific papers and internal reports.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• BS with3+ years' experience
• Experience in analytical separations methods such as HPLC,uHPLC, cIEF, or CGE.
• Experience with assay development/qualification/validation, pharmacopeia compliance, and analytical life cycle management.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

• Understandingofthe biopharmaceutical product lifecycle.
• Experience with analytical support of challenging biopharmaceutical formulations
• Knowledgeofprotein analytical & biochemical techniques such as HPLC, UPLC, capillary electrophoresis, LC-MSor 2D-HPLC.

*LI-GSK

GSKBiopharm_Development

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