MSAT Digital and Data Specialist

Site Name: USA - Pennsylvania - Marietta
Posted Date: Jun 5 2026

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 lead design, qualification, validation and troubleshooting of single use systems for drug substance manufacturing. You will work closely with manufacturing, quality, engineering, supply chain and external suppliers. We value clear problem solving, practical technical skills and collaboration. This role offers visible impact, technical ownership and opportunities to grow across projects and teams while helping GSK get ahead of disease together.

Responsibilities

The Digital and Data Analyst will support the MSAT organization by leveraging digital tools and data analytics to optimize manufacturing processes, improve product quality, and ensure regulatory compliance within the vaccine manufacturing site.

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:

• Develop and Implement Data Analytics Solutions: Design and deploy data analytics models to monitor and enhance manufacturing processes, ensuring data-driven decision-making.

• Collaborate with Cross-Functional Teams: Work closely with departments such as Quality, Operations, and IT to identify data needs, integrate data sources, and develop comprehensive analytics solutions.

• Utilize Digital Tools: Implement and manage digital tools for automated data collection, real-time monitoring, and advanced analytics to streamline manufacturing operations.

• Ensure Data Integrity and Accuracy: Maintain high standards of data quality by validating data sources, performing regular audits, and ensuring accurate data entry and processing.

• Support Digital Transformation Initiatives: Lead and participate in projects aimed at digitalizing manufacturing processes, enhancing data accessibility, and improving overall efficiency.

• Provide Training and Support: Educate team members on the use of data analytics tools and techniques, fostering a data-driven culture within the organization.

• Support Root Cause Analysis: Analyze process deviations and quality issues using data analytics to identify root causes and recommend corrective and preventive actions.

• Maintain Industry Knowledge: Stay updated with the latest trends, technologies, and best practices in data analytics and digital transformation to continuously improve processes.

• Ensure Regulatory Compliance: Adhere to regulatory requirements and company policies in all data-related activities, ensuring compliance with industry standards.

• Prepare and Present Insights: Compile and present data-driven insights and reports to stakeholders, supporting strategic decision-making and continuous improvement initiatives.

Why You?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• Bachelor's degree in engineering, pharmaceutical sciences, chemistry or related technical discipline.
• 3+ years' experience in pharmaceutical or biopharma manufacturing focused on single use systems or disposables.
• Experience in qualification, validation or technical transfer of single use systems.
• Experience preparing and executing technical protocols, reports and GMP documentation.

Preferred Qualification
If you have the following characteristics, it would be a plus:

• Advanced degree in engineering, pharmaceutical sciences or related field.
• Knowledge of regulatory guidance and industry standards for extractables, leachable and sterility.
• Experience working cross-functionally with operations, quality and suppliers.

• Proficiency in Data Analytics Software: Advanced skills in programming languages and tools such as Python, R, SQL, and data visualization tools like Power BI.

• Experience with Digital Tools and Platforms: Familiarity with Manufacturing Execution Systems (MES), Laboratory Information Management Systems (LIMS), and other digital platforms used in manufacturing environments like SAP.

• Strong Problem-Solving and Analytical Skills: Ability to analyze complex data sets, identify trends, and develop actionable insights to improve manufacturing processes.

• Excellent Communication and Collaboration Abilities: Strong verbal and written communication skills to effectively convey data-driven insights to stakeholders and collaborate with cross-functional teams.

• Knowledge of Regulatory Requirements: Understanding of regulatory standards and compliance requirements in the pharmaceutical and vaccine manufacturing industry.

• Project Management Skills: Ability to manage multiple projects simultaneously, prioritize tasks, and meet deadlines.

• Attention to Detail: High level of accuracy and attention to detail in data analysis and reporting.

• Continuous Learning and Adaptability: Willingness to stay updated with the latest industry trends, technologies, and best practices in data analytics and digital transformation.

• Critical Thinking: Ability to think critically and independently to solve problems and make data-driven decisions.

• Technical Writing: Proficiency in documenting processes, creating standard operating procedures (SOPs), and preparing technical reports.

What we value in you
We put safety and quality first. We seek people who are practical, curious and open to learning. You will join a team that collaborates across roles and improves how we work. We welcome applicants from all backgrounds and encourage people who bring different perspectives to apply.

Work arrangement
This position is on-site in the United States. Hybrid or remote work may not be available for this role.

Ready to apply?
If this role fits your skills and ambition, we want to hear from you. Please submit your resume and a short note describing a recent SUS qualification, validation or troubleshooting project you led or supported. We look forward to learning about you.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

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.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - View email address on click.appcast.io

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at