GSK is seeking a QA MES Specialist in Marietta, Georgia, to lead quality activities related to Manufacturing Execution Systems (MES) and digital quality tools. Candidates should have a background in quality, manufacturing, or digital systems within a regulated environment, with a focus on compliance and data integrity
Job Summary
This role leads quality activities for Manufacturing Execution Systems to ensure compliant production and accurate data.
The position requires partnering with manufacturing, engineering, IT, validation, and quality teams to support inspection readiness.
GSK is a global biopharma company committed to uniting science, technology, and talent to get ahead of disease together.
Matching Summary
Match Score: 85
GSK is seeking a QA MES Specialist in Marietta, Georgia, to lead quality activities related to Manufacturing Execution Systems (MES) and digital quality tools. Candidates should have a background in quality, manufacturing, or digital systems within a regulated environment, with a focus on compliance and data integrity.
Skills & Requirements
Must-have
Manufacturing Execution System experience
Electronic batch records review
Regulated life sciences environment
Change control and deviation support
Root cause analysis skills
Nice-to-have
MES implementation or configuration experience
DQ/IQ/OQ/PQ validation lifecycle knowledge
Strong coaching and influence abilities
Formal training in investigation techniques
Experience with electronic document management systems
Key Requirements
Bachelor's degree in technical, scientific, or quality-related field
2+ years experience in regulated life sciences quality or manufacturing