Biopharm Manufacturing Associate II

Overview

Site Name: USA - Pennsylvania - King of Prussia

Posted Date:
Jan 26 2026

We make and supply medicines and vaccines around the globe. 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 scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021. We continue to modernize to launch more products quickly and to turbo-charge delivery across our portfolio with a focus on quality, safety, and service.

We aim to harness automation and robotics for smarter work and faster innovation in our R&D pipeline.

As a Biopharm Manufacturing Associate II, you will 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. You will complete daily manufacturing tasks and increase competency across production areas over time. You will participate in safety and compliance initiatives, as well as investigations, and engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance.

The purpose of this role is to be part of a dynamic, multi-tiered operations team that brings life-changing and life-saving medicine to patients. You will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) daily by engaging positively with team members and production support groups. Under the direction of senior personnel, you will perform a variety of large scale production operations, interact with automated equipment, and monitor/process data.

You will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. You will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts. You will work with these teams to continuously improve safety, quality, and schedule/cost performance.

This role will provide you the opportunity to lead key activities to progress your career. Responsibilities include some of the following:

• Demonstrate GSK Values – Patient Focus, Transparency, Respect, and Integrity – in every interaction and task, and 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 to execution. These activities are primarily within the production suite, but may require out-of-suite or off-site work (e.g., FAT support).
• Monitor equipment and critical process parameters, escalate issues or abnormalities, and participate in troubleshooting activities.
• Strive to maintain a high level of competency with current and emerging digital platforms (SAP, E , AR/VR, etc.).
• By learning the production schedule and assessing it daily, proactively ensure all processing equipment and necessary materials are adequate and available to set the team up for success.
• Transparently participate in investigations that result from safety or compliance issues.

Basic qualifications:

• BS/BA degree, with cGMP manufacturing experience
• Or an Associate’s degree from Montgomery County Community College in Biotechnology or related technical field with cGMP manufacturing experience
• Or High School degree, 1+ years of cGMP manufacturing experience

Preferred Qualifications:

• Demonstrated level of high performance
• Strong verbal and written skills
• The ability to work well in a…