Work Preference
Professional Summary
Overview
Work History
Education
Skills
Timeline
Personal Information
Open To Work

Andrew Rogers

PAI Pharma
Apex,NC

Work Preference

Job Search Status:

Open to work

Desired Job Title

Quality Control Chemist

Work Type

Full Time

Location Preference

On-Site

Location:

Apex, NC

Open to relocation:

Yes

Minimum Desired Compensation

$70000/yr

Important To Me

Career advancementWork-life balanceCompany CultureHealthcare benefitsPaid time off
10
years of professional experience

QC Chemist III at PAI Pharma managing pharmaceutical quality control testing for controlled substances, raw materials, finished products, and both long term and accelerated stability samples. Applies HPLC, FTIR, Karl Fisher, GC, and other wet chemistry methods while documenting results in LIMS, OpenLab, and Empower. Supports compliant laboratory operations through DEA, FDA, cGMP, ALCOA++, SOP, and Data Integrity adherence while also mentoring junior chemists on impurity processing and data interpretation.

Work History

QC Chemist III

1 Year 10 Months
PAI Pharma | 11.2024 - Current
  • Maintain laboratory data systems while supporting daily testing and review workflows.
  • Handle controlled substances in compliance with DEA, FDA, and cGMP requirements.
  • Analyze raw materials and finished products using HPLC, FTIR, and GC to support product quality.
  • Mentor junior chemists on experimental design, data analysis, data integrity, and interpretation to strengthen team capability.
  • Use Starlims, OpenLab, and Empower to organize laboratory data and support accurate reporting.
  • Apply SOPs and method documentation practices to maintain consistent testing and interpretation across analyses.

QC Chemist II

6 Years 9 Months
PAI Pharma | 02.2018 - 11.2024
  • Complete advanced analyses using HPLC, GC, FT-IR, and UV-Vis while meeting deadline-driven workloads.
  • Optimize weekly workload to complete advanced tasks within deadlines and improve laboratory efficiency.
  • Manage chemicals, reagents, and supplies to keep inventory stocked for ongoing testing and production needs.
  • Apply cGMP compliance and FDA regulations to support quality control, data integrity, and deviation reporting.
  • Support laboratory coordination by documenting methods, maintaining records in Empower Software, and using Starlims for sample tracking.
  • Coordinate with colleagues to troubleshoot analytical issues, support mentoring, and keep testing workflows moving efficiently.

QC Chemist I

3 Years 8 Months
PAI Pharma | 02.2018 - 10.2021
  • Conduct titrations, assays, and distillation on raw materials to verify composition and support quality control.
  • Use pH meter, FT-IR, UV-Vis, refractometer, and melting point apparatus to deliver precise analytical results.
  • Apply Empower Software to document test results and maintain data integrity across laboratory records.
  • Handle hazardous waste and dispose of materials in line with EPA compliance requirements.
  • Support cGMP documentation and method recording to keep laboratory work aligned with regulatory standards.

In Process Quality Coordinator

1 Year 4 Months
PAI Pharma | 10.2016 - 02.2018
  • Organized complex tasks efficiently, using strong time management to improve day-to-day workflow.
  • Collaborated with manufacturing to uphold cGMP standards and support consistent product quality.
  • Applied clear communication to work effectively in both individual and team environments.
  • Maintained consistent quality control focus while supporting organized, efficient execution of daily responsibilities.
  • Supported data integrity practices through careful documentation and reliable follow-through on assigned work.

Education

Bachelor of Science - Chemistry

Erskine College | Due West, SC | 06-2016

Skills

High-Performance Liquid Chromatography
Gas Chromatography
FTIR Spectroscopy
UV-Vis Spectroscopy
Empower Software
LIMS
Quality control
cGMP compliance
FDA regulations
Deviation reporting
Data integrity
Mentorship
SOP development
Cross-functional collaboration
Method documentation
Laboratory coordination
Analytical method validation
Stability studies
Dissolution testing
Data integrity practices
USP compendial methods

Timeline

QC Chemist III

PAI Pharma
11.2024 - CurrentRead More

QC Chemist II

PAI Pharma
02.2018 - 11.2024Read More

QC Chemist I

PAI Pharma
02.2018 - 10.2021Read More

In Process Quality Coordinator

PAI Pharma
10.2016 - 02.2018Read More

Erskine College

Bachelor of Science from Chemistry
Read More

Personal Information

Title: QC Chemist III | HPLC, FTIR, Quality Control

Andrew Rogers