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 Communica
Benefits
Health insurance
Additional Information
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.
Gsk · US