At GSK, we are ambitious for patients. As the healthcare landscape continues to evolve—bringing new stakeholders, data sources, and expectations—we are committed to ensuring that the patient voice meaningfully informs how medicines are developed, evaluated, launched, and delivered to patients. This includes patient engagement across drug development, regulatory decision-making, health technology assessment, launch planning, and patient care.
This role is responsible for the manufacture of biopharmaceutical analytical reference materials and supports the R&D biopharmaceutical critical reagents program in line with regulatory and business requirements.
This role will provide you the opportunity to lead key activities to progress your career. These responsibilities include some of the following:
Why you?
Basic Qualifications:
Preferred Qualifications:
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Tagged as: Life Sciences
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