Drimva

GSK

Quality Unit Business Process Specialist

USA - Pennsylvania - Marietta · On-site · Full-time · Posted Aug 31, 2026

Experience
3–5 years in cGMP production or quality control for cGMP manufacturing; 1–3 years designing or implementing business processes or SAP systems.
Education
Bachelor’s degree in life sciences, engineering, quality, or a related technical field.

About the job

Provides quality oversight of SAP and related manufacturing business processes and systems, ensuring compliance and driving process improvement at a U.S. manufacturing site.

What you'll do

  • Oversee Production and QC SAP use, master data, business rules, and compliance; serve as a site SAP quality consultant.
  • Design, document, maintain, and improve quality processes and SOPs; train users and support cross-functional implementation.
  • Support change control, risk assessments, investigations, root cause analysis, CAPA, and quality metrics related to SAP and process changes.

What they ask for

  • 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.
  • Practical experience with procedures or process documentation, GMP/GDP, and change control, CAPA, or deviation investigations.

Nice to have

  • Experience in biologics or pharmaceutical manufacturing with computerized systems or digital manufacturing tools such as MES, LIMS; or Green belt certification.
  • Experience with risk assessment, structured root cause analysis, coaching colleagues, or quality KPIs.

Tools

SAP, MES, LIMS, CAPA

Model-written summary · the original posting is authoritative

First seen Oct 28, 2026 · Last verified Nov 5, 2026 (UTC)