Rob Ericksen

Background

About Rob Ericksen

A well-seasoned Senior Chemist that develops, validates, and transfers analytical test methods in both QC and R&D environments. Proficient in chromatographic systems, including HPLC, GC, and IC; with hands-on experience in equipment maintenance and validation. Adept at maintaining regulatory compliance to cGMP, FDA, and DEA standards. Skilled in testing drug substances and products; performing data verification and peer review for batch records and stability studies. Strong technical writing and communication abilities with a proven track record of leadership and mentoring teams. Committed to enhancing operational efficiency and maintaining quality in the following fields- Analytical Testing (HPLC/UPLC, GC, IC)- Method Validation & Transfer - Data Verification & Review - Computer Systems Validation (CSV)- Regulatory Compliance - Elemental Analysis (ICP-MS, OES)- Quality Control & Quality Assurance - Good Laboratory Practices (GLP)- Periodic Review of Procedures - Method Development - Batch Record Review - Stability Trending & Analysis - Operational Efficiency