Gracee Presley-Stancer
Client Partner Director @ Verista
- Role
- Client Partner at Verista
- Location
- Wichita, KS, US
- LinkedIn followers
- 500 followers
About Gracee Presley-Stancer
A results-driven Project Manager and Manufacturing Solutions Service Line Director with a proven record of leading complex aseptic, automation, and validation projects across the pharmaceutical industry.My expertise spans: Component Processing Equipment – washers, autoclaves, depyrogenation tunnels, stopper processors VHP Generators & Isolators – design, integration, and validation for aseptic environments Automation & SCADA – system integrations, upgrades, and lifecycle management CSV/CSA – risk-based approaches that streamline compliance while ensuring data integrityAs a Service Line Director, I balance project delivery with building people and capabilities. I mentor teams of engineers, validation professionals, and project managers—developing local pipelines, training new leaders, and aligning career growth with Verista’s strategic goals. Core Strengths Leading cross-functional teams in CQV, CSV/CSA, automation, SCADA, and digital validation Applying risk-based validation approaches (CSA, FMEA, QRA, BRA) to focus resources where they matter most Driving service line expansion with SME-based roles and client specific solutions Developing people through structured mentorship, training, and role-based career planning
Experience
Client Partner
Jan 2026 — Present · US
Client Partner at Verista focused on scaling strategic partnerships, expanding market opportunities, and delivering integrated CQV, CSV/CSA, engineering, and digital solutions that advance pharmaceutical innovation and operational excellence.
Education
Wichita State University
Bachelor's degree, Biomedical/Medical Engineering
2011 — 2014
Skills
- Quality Control
- Gmp
- Databases
- Document Review
- Employee Training
- Investigation
- Change Management
- Elisa
- Microbiology
- Endotoxin
- Change Control
- Data Analysis
- Training
- Method Development
- Standard Operating Procedure (Sop)
- Validation
- Quality Assurance
- Corrective and Preventive Action (Capa)
- Regulatory Compliance
- Kpi Implementation
- Batch Processing
- Pharmaceutical Microbiology
- Genotyping
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