About this Candidate
DAVRON CV: Candidate 3811484
MANUFACTURING SUPERVISOR | PHARMA & BIOTECH OPERATIONS | cGMP PRODUCTION LEAD
Core Expertise
- Supervised production shifts and teams exceeding 20 employees to meet production targets
- Ensured cGMP, OSHA, EPA, TTB, and EHS compliance in manufacturing operations
- Implemented process improvements and documentation streamlining to boost line efficiency
- Managed deviations, root-cause analysis, change controls, and CAPA execution
- Performed hands-on upstream and downstream operations including autoclave and tank cleaning
Project Background
- Led shift exchanges and one-on-one coaching to adapt staffing and performance
- Reduced downtime by coordinating production and maintenance through proactive communication
- Improved documentation workflows, accelerating release of batch records and quality reports
- Managed material consumption and quality documentation in ERP systems under tight timelines
- Executed validated cleaning and milling procedures for upstream and downstream manufacturing
Key Skills
- cGMP | SOPs | CAPA | Deviation Management
- Upstream & Downstream Processing | Autoclave | Tank Cleaning | Blending
- Manufacturing Systems: SAP | JDE | MRP
- Process Improvement | Root Cause Analysis | Change Control
- Equipment: Fitz mills | Weighing & Dispensing | Process Controls
- MS Office (Excel, Word) | Batch Record & Documentation Management
Why Interview this Candidate?
They combine 14+ years of hands-on upstream/downstream manufacturing with proven supervisory experience leading teams over 20 people. Known for reducing downtime through cross-functional collaboration and improving throughput by streamlining documentation and workflows. Their blend of floor-level technical skill and compliance-first leadership enables rapid stabilization and measurable gains in regulated production environments.
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