Muna Ahmed
Galloway
Summary
Detail-oriented Quality Control Scientist II with 3 years of GMP experience in commercial drug manufacturing. Expertise includes analytical testing, quality investigations, and compliance-driven laboratory operations. Collaborates effectively with cross-functional teams to uphold product quality and regulatory standards while ensuring timely batch release.
Overview
5
5
years of professional experience
Work History
Scientist II - Quality Control
Hikma Pharmaceuticals
01.2023 - Current
- Review analytical data for accuracy and compliance with FDA cGMP requirements.
- Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using approved methods.
- Reviewed analytical data to ensure accuracy and compliance with FDA cGMP requirements, contributing to quality assurance.
- Perform instrument calibration, maintenance, troubleshooting, and qualification.
- Supported investigations of deviations and OOS results, collaborating with Quality Assurance to uphold product integrity.
- Performed calibration, maintenance, and troubleshooting of instruments, ensuring reliable operation and compliance with regulatory standards.
- Follow SOPs and collaborate with QA, Validation, and Regulatory teams.
Laboratory Technician
LabCorp
01.2022 - 01.2023
- Performed high-volume PCR testing in a regulated laboratory.
- Analyzed patient results using LIMS to support timely diagnosis and treatment.
- Calibrated and troubleshot laboratory equipment to ensure reliable testing outcomes.
- Documented procedures and maintained SOP compliance to uphold laboratory quality standards.
Education
Masters of Biomedical Sciences -
Geisinger Commonwealth School of Medicine
Scranton01-2021
Bachelor of Arts - Biology
Otterbein University
Westerville01-2018
Skills
- HPLC
- UPLC
- Empower
- UV-Vis
- Dissolution
- Disintegration
- NIR
- FDA cGMP
- GDP
- Data integrity
- Quality assurance protocols
- Data analytic
- Statistical analysissssssssssssssssss
CORE COMPETENCIES
Quality Control, FDA cGMP, Data Integrity (ALCOA+), Quality Investigations support, SOP Compliance, CAPA Support, Root Cause Analysis, Cross-Functional Collaboration, Regulatory Inspection Readiness.
Timeline
Scientist II - Quality Control
Hikma Pharmaceuticals
01.2023 - Current
Laboratory Technician
LabCorp
01.2022 - 01.2023
Bachelor of Arts - Biology
Otterbein University
Masters of Biomedical Sciences -
Geisinger Commonwealth School of Medicine