About this Candidate
DAVRON CV: Candidate 1915417
SENIOR MANUFACTURING SUPERVISOR | GMP PHARMA OPERATIONS, CIP/SIP & CONTINUOUS IMPROVEMENT
Core Expertise
- GMP-compliant batch manufacturing and aseptic sampling with strict documentation and traceability.
- Operation and troubleshooting of CIP/SIP systems and aseptic production equipment for uptime.
- Led material-handling innovation that reduced waste and delivered $2M annual savings.
- Implemented continuous improvement, 5S, Lean and Six Sigma methods to raise efficiency.
- Supervised cross-functional teams, training and mentoring production staff in regulated environments.
Project Background
- Designed and validated a bag-contained filtration machine prototype to minimize product loss.
- Managed electronic batch records and GDP/GMP paperwork to ensure audit-ready production runs.
- Led continuous process improvement teams to resolve root causes and restore production swiftly.
- Operated and maintained autoclaves, COP washers, and production equipment under CGMP.
- Directed supplier quality assessments, PPAP/APQP-related inspections and ISO-aligned internal audits.
Key Skills
- GMP | GDP | CGMP | ISO 9001 | ISO 13485
- Lean Manufacturing | Six Sigma | 5S | Continuous Improvement | Root Cause Analysis
- Electronic Batch Records | ERP | MRP | Production Planning
- CIP/SIP operation | Autoclave | COP washer | Aseptic sampling
- PPAP | APQP | Supplier assessments | Internal audits | Quality assurance
- GD&T | Plastics injection molding | Functional testing | Process troubleshooting
Education
- A.A., Criminal Justice — Central Georgia Technical College
Awards & Recognition
- Six Sigma Certification
Why Interview this Candidate?
Experienced manufacturing supervisor with deep regulated-industry expertise in GMP operations, CIP/SIP systems, electronic batch management, and continuous improvement. Demonstrated ability to design practical equipment solutions and lead cross-functional teams, yielding measurable cost savings and waste reduction. Strong record of training, audits compliance, and rapid root-cause resolution to keep production audit-ready and reliable.
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