Summary
Overview
Work History
Education
Skills
References
Timeline
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Maha Barsoum

Maha Barsoum

65 Beech Park, Cahir

Summary

Results-driven and detail-oriented Senior QC Chemist with extensive experience in the pharmaceutical industry and a strong foundation in GMP-regulated environments. Skilled in performing and interpreting complex QC analyses using techniques such as HPLC, GC, FTIR, and UV spectroscopy. Adept at ensuring regulatory compliance, driving continuous improvement, and supporting audit readiness. Currently pursuing a Master’s in Pharmaceutical Manufacturing Technology at Trinity College Dublin, further strengthening my expertise in quality systems and manufacturing processes. Recognised for strong leadership, clear communication, and a collaborative approach to problem-solving and team development.

Overview

4
4
years of professional experience

Work History

Sr. Quality Control Analyst

Pinewood Healthcare,
Clonmel
12.2023 - Current
  • Documented all quality control activities, results, and corrective actions taken.
  • Trained analysts in laboratory procedures and assays; maintained training records for FP analysts.
  • Compiled laboratory test data, performed analyses, and assisted in the batch release process.
  • Conducted stability testing and validation testing of finished products.
  • Assisted in investigations and closeouts of out-of-specifications and out-of-trend results, recommending corrective actions.
  • Identified and troubleshooted equipment problems, ensuring accurate results and process integrity.
  • Monitored and upheld safe operating procedures and clean area mandates to meet regulatory requirements.
  • Maintained lab cleanliness and safety standards.

Quality Control Analyst

Sanofi
Co. Waterford
01.2023 - 06.2023
  • Performed quality control testing on finished products and stability samples using various analytical instruments, ensuring adherence to established procedures and regulatory guidelines.
  • Collaborated with cross-functional teams to support product release, stability studies, and regulatory submissions.
  • Maintained accurate and comprehensive documentation, including test records, data analysis, and reports.
  • Participated in audit readiness and regulatory documentation reviews.
  • Assisted in laboratory activities, including sample preparation, instrument setup, and data entry.
  • Investigated and resolved out-of-specifications and out-of-trend results, conducted root cause analysis, and implemented corrective actions.
  • Maintained and calibrated laboratory equipment, ensuring accurate and reliable test results.
  • Analysed customer complaints and feedback to determine the root causes of problems and develop solutions.
  • Followed safety procedures, and maintained a clean and organised laboratory environment.

Analyst on Contract

Complete Laboratory Solutions
Galway
12.2020 - 06.2023
  • Performed quality control testing on finished products and stability samples using various analytical instruments, ensuring adherence to established procedures and regulatory guidelines
  • Collaborated with cross-functional teams to support product release, stability studies, and regulatory submissions
  • Maintained accurate and comprehensive documentation, including test records, data analysis, and reports
  • Assisted in laboratory activities, including sample preparation, instrument setup, and data entry
  • Investigated and resolved out-of-specifications and out-of-trend results, conducted root cause analysis, and implemented corrective actions.
  • Maintained and calibrated laboratory equipment, ensuring accurate and reliable test results
  • Followed safety procedures, and maintained a clean and organised laboratory environment.

Quality Control Analyst

Pinewood Healthcare
Clonmel
05.2021 - 12.2022
  • Conducted quality control testing on raw materials, in-process, and finished products using HPLC, GC, UV spectroscopy, FTIR, Karl Fischer, etc.
  • Maintained laboratory equipment, and ensured calibration and validation were up to date.
  • Documented all testing results, and maintained accurate and organised records.
  • Participated in internal and external audits and inspections, and assisted in the resolution of any findings or observations.
  • Conducted routine and non-routine analyses of raw materials, in-process samples, and finished products to assess quality and compliance.
  • Conducted investigations into out-of-specification results, and recommended corrective actions.
  • Trained new employees in laboratory procedures, quality control techniques, and safety protocols.
  • Assisted in writing and maintaining documentation.

Education

Master of Science - Pharmaceutical Manufacturing Technology

Trinity College Dublin
Dublin, Ireland
01-2027

Bachelor of Science - Pharmaceutical Science With Drug Development

I.T. Sligo
Sligo
06-2020

Skills

  • Batch Release: Proficient in assisting with batch release processes, ensuring product quality and compliance with specifications
  • Stability and Validation Testing: Experienced in conducting and assisting with stability and validation testing of finished products
  • Investigation and Corrective Actions: Skilled in conducting investigations for out-of-specifications and out-of-trend results and implementing corrective actions
  • Equipment Troubleshooting: Strong ability to identify, troubleshoot, and resolve equipment-related issues in a laboratory environment
  • Regulatory Compliance: Knowledge of regulatory requirements including cGMP, FDA, HPRA, and ICH guidelines, ensuring compliance in all testing and documentation processes
  • Data Analysis and Interpretation: Experienced in compiling, analysing, and interpreting laboratory test data to ensure accuracy and compliance
  • Training and Mentorship: Adept at training new analysts on laboratory procedures, ensuring competency in all testing processes
  • Documentation and Review: Skilled in documentation of quality control activities, results, and corrective actions, ensuring adherence to company standards and regulatory requirements
  • Proficient in Microsoft Office and Laboratory Software: Advanced proficiency in Microsoft Office Suite and laboratory software such as LIMS, Lab Solutions, and Empower for efficient data management and analysis

References

References available upon request.

Timeline

Sr. Quality Control Analyst

Pinewood Healthcare,
12.2023 - Current

Quality Control Analyst

Sanofi
01.2023 - 06.2023

Quality Control Analyst

Pinewood Healthcare
05.2021 - 12.2022

Analyst on Contract

Complete Laboratory Solutions
12.2020 - 06.2023

Master of Science - Pharmaceutical Manufacturing Technology

Trinity College Dublin

Bachelor of Science - Pharmaceutical Science With Drug Development

I.T. Sligo
Maha Barsoum