QA MES Specialist

Location:

USA - Pennsylvania - Marietta

Posted Date:
Jun 4 2026

You will lead quality activities for Manufacturing Execution Systems (MES) and related digital quality tools. You will partner with manufacturing, engineering, IT, validation, and quality teams. You will ensure MES supports compliant production, accurate data, and inspection readiness. This role offers growth, real impact on product quality, and alignment with our mission of uniting science, technology, and talent to get ahead of disease together.

• Lead MES quality activities including system configuration reviews, electronic batch record checks, and system change control support.
• Review MES-generated records and reports to confirm completeness, data integrity, and compliance with procedures.
• Support investigations of deviations linked to MES or digital systems. Perform root cause analysis and track corrective actions.
• Partner with validation and IT to ensure MES changes link to DQ/IQ/OQ/PQ or equivalent validation steps and documentation.
• Coach manufacturing and lab teams on good documentation practices, electronic record keeping, and system use on the shop floor.
• Maintain inspection-ready MES records and contribute to quality KPI trending and continuous improvement initiatives.
• Support readiness for internal and external audits, provide clear documentation, and act as a subject matter contributor during inspections.
• Manage supplier and third-party quality expectations for MES vendors and integrators, ensuring timely resolution of issues.

• Bachelor's degree in a technical, scientific, or quality-related field, or equivalent experience.
• 2+ years experience in quality, manufacturing, or digital systems within a regulated life sciences environment.
• Experience with MES, electronic batch records, or other manufacturing execution or electronic quality systems.
• Experience supporting change control, deviations, CAPA, or document management in a regulated environment.

• Bachelor’s degree in engineering, life sciences, information systems, or a related field.
• Experience with MES implementation, configuration, or validation in pharma or biotech.
• Understanding of DQ/IQ/OQ/PQ or equivalent validation lifecycle and how it ties to quality systems.
• Experience with electronic document management systems or quality management software.
• Formal training in root cause analysis methods or investigation techniques.
• Ability to coach and influence operational teams and to present technical information clearly.
• Strong written and verbal communication skills and the ability to work across functions.
• Practical knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP), including data integrity principles.

This role requires On‑site presence and will be required for hands‑on MES support, validation activities, and shop‑floor coaching. Minimum 4 days weekly on site.

We offer a comprehensive benefits program for US employees.

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.