Quality Unit SAP & Process Excellence Specialist

GlaxoSmithKline; Marietta (PA); On-site; USD 110,000 - 140,000; Full time

Job summary

GlaxoSmithKline in the United States seeks a Quality Unit Business Process Specialist to supervise SAP quality processes and master data, ensuring alignment with cGMP standards. The role partners with operations, engineering, IT and quality teams to design and sustain compliant, reliable processes across production.

We value practical, curious professionals who can coach others and translate business needs into documented workflows. On-site at a U.S.

Qualifications

• Bachelor's degree in life sciences, engineering, quality, or a related technical field.
• 3-5 years’ experience in cGMP production or quality control for cGMP manufacturing.
• 1-3 years’ experience designing or implementing business processes or SAP systems.

Responsibilities

• Act as the Quality Assurance oversight to Production SAP use, business rules, outcomes and compliance including creation of new material master data.
• QA Oversight for Serialization Line client recipe creation and modification.
• Key contact for internal departments and other sites for information and assessment and distribution regarding master data.
• Act as site Quality Consultant for SAP when issues arise.
• Provide input to global procedural revisions to address site Master Data needs.
• Act as Quality Assurance oversight of QC Master Data, adhering to procedures and CFR requirements.
• Train users related to SAP business processes.
• Lead the design, documentation and maintenance of quality unit business processes and SOPs.
• Monitor quality metrics and trends and recommend improvements to reduce risk.

Skills

cGMP knowledge

SAP experience

Cross-functional collaboration

Documentation writing

Quality systems

Data integrity

Education

Bachelor's degree in life sciences

Tools

SAP

Job description

GlaxoSmithKline in the United States seeks a Quality Unit Business Process Specialist to supervise SAP quality processes and master data, ensuring alignment with cGMP standards. The role partners with operations, engineering, IT and quality teams to design and sustain compliant, reliable processes across production.

We value practical, curious professionals who can coach others and translate business needs into documented workflows. On-site at a U.S.