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MSAT Digital and Data Specialist

Job in Pittsburgh, Allegheny County, Pennsylvania, 15289, USA
Listing for: GlaxoSmithKline
Full Time position
Listed on 2026-06-11
Job specializations:
  • IT/Tech
    Data Analyst
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Site: USA - Pennsylvania - Marietta

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
  • 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.
Basic Qualifications
  • 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 Qualifications
  • 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…
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