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GSK

MSAT Product Owner Associate Director

GSK, King Of Prussia, Pennsylvania, United States, 19406

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Overview

Site Name: USA - Pennsylvania - King of Prussia Posted Date: Sep 25 2025 At GSK, we manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is vital to bringing our innovations to patients quickly, efficiently and effectively. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. We are looking to hire an

MSAT Product Owner Associate Director

to join the Manufacturing Science and Technology (MSAT) organization in Upper Merion. This is a site-based team, providing technical support to ensure Upper Merion Biopharm site goals and objectives are reached. The primary objective of MSAT is to ensure manufacturing processes are capable, compliant and productive while ensuring product quality. The site MSAT team is responsible for delivering continuous improvements to the existing supply chains supported by UM Biopharm and working with global MSAT to execute technology transfers and implement process-related improvement programs across the product lifecycle. The

MSAT Product Owner Associate Director

will lead a team of product owners to support the portfolio of clinical and commercial programs for Upper Merion. Product Owners are the single point of accountability for technology transfer, product lifecycle, CMC strategy, and technical execution for the biopharmaceutical assets manufactured at Upper Merion. The role supports the team to manage new product introductions, QbD, control strategy, and CPV development and maintenance, CMC dossier authoring and health authority questions, and technical product strategy and process efficiency / continuous improvements. The individual is also expected to drive continuous improvement in these spaces, aligning with platform standards and integrating digital solutions. In addition, this role requires working in a cross-functional matrix environment, including stakeholders in other departments within UM Biopharm (e.g., production, quality, engineering), and global MSAT, R&D, global regulatory, and global quality. This role will provide you the opportunity to lead key activities to progress your career; responsibilities include some of the following:

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