Biopharmaceutical Manufacturing Associate II

About the role

We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021. We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. As a Biopharm Manufacturing Associate II, you will be part of a dynamic, multi‑tiered operations team that brings life‑changing and life‑saving medicine to patients around the world, demonstrating GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) daily.

Responsibilities

• Perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep.
• Complete daily manufacturing tasks and increase competency in different production areas over time.
• Participate in safety and compliance initiatives and investigations.
• Engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance.
• Demonstrate GSK Values (Patient Focus, Transparency, Respect, Integrity) in every interaction and work task.
• Live GSK’s Expectations of Courage, Accountability, Development, and Teamwork to achieve high‑performing behaviors.
• With good documentation and data integrity practices, safely and compliantly complete and document daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks.
• Proactively work with senior staff to achieve competency in production operations.
• Support cross‑functional activities such as engineering actions, validation actions, and Tech Transfer actions, including proactive safety and compliance input prior