MSAT Technology SME
Job in
Marietta, Lancaster County, Pennsylvania, 17547, USA
Listed on 2026-06-03
Listing for:
GSK
Full Time
position Listed on 2026-06-03
Job specializations:
-
Engineering
Validation Engineer, Manufacturing Engineer, Process Engineer, Quality Engineering
Job Description & How to Apply Below
Business Introduction
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 not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. 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.
Position Summary
You will join Manufacturing Science & Technology (MSAT) as a Technology Subject Matter Expert (SME) in the United States. You will work across technical, quality and other partners to support commercial Drug Substance and Drug Product Vaccine manufacture with technical lifecycle ownership in your area of expertise (i.e. mixing/homogeneity, ultrafiltration/diafiltration, chromatography, formulation, aseptic filling and AVI). You will support technical strategy, troubleshooting, manufacturing scale-up activities, process robustness initiatives, and technology transfers from donor sites for new and established products.
We value clear problem solvers who communicate well, act with integrity, and who want to grow while making a real impact on patient supply.
This role offers growth, visible impact across global supply, and the chance to help GSK unite science, technology and talent to get ahead of disease together.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Support technical strategy, troubleshooting, manufacturing scale-up activities, process robustness initiatives, technology transfers., lifecycle changes and technical reviews.
- Support cross functional teams for investigations, root cause analysis, corrective and preventive actions, and regulatory responses.
- Translate lab and development knowledge into robust, scalable manufacturing processes.
- Design and run experiments for process characterization, optimization and validation.
- Support inspection readiness and audit activities.
- Support the deployment of process control strategies, performance standards, and lifecycle monitoring for manufacturing processes.
- Provide technical input to change controls, risk assessments and corrective actions.
- Train, coach, and mentor cross-functional teams to build skills.
- Support continuous improvement by identifying technical improvements and supporting implementation.
Work arrangement
This role is hybrid. You will be expected to be on-site regularly to support manufacturing and operational readiness activities as well as technical transfer work. Exact on-site vs remote days will be agreed with your manager based on project needs.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelor's degree in a relevant scientific or engineering discipline such as Pharmaceutical Sciences, Chemical Engineering, Biology, or Chemistry.
- 2+ years' experience in pharmaceutical vaccines or biologics manufacturing technical operations.
- Hands-on experience with technology transfers, scale-up, process validation, and lifecycle management in a regulated environment.
- Practical knowledge of unit operations such as mixing/homogeneity, chromatography, filtration, ultrafiltration/diafiltration, and aseptic processing.
- Experience using data analysis and basic statistical methods for process understanding.
- Knowledge of GMP and regulatory expectations relevant to manufacturing and quality systems.
If you have the following characteristics, it would be a plus:
- Master's degree or PhD in a relevant scientific or engineering field.
- Experience with sterile manufacturing and aseptic processing.
- Familiarity with process control systems, manufacturing informatics or data historians.
- Knowledge of regulatory expectations for process validation and continued process verification.
- Proven track record of delivering continuous improvement or yield enhancement projects.
- Strong written and verbal communication skills and experience preparing technical reports and protocols.
- You explain technical ideas clearly and help others learn.
- You take ownership and act with integrity.
- You welcome different perspectives and support inclusion.
- You balance quality, speed and risk when deciding.
- You stay curious and seek opportunities to grow.
If this role fits your experience and ambitions, we want to hear from you. Please submit your application and tell us…
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