Analyst with a strong focus on data integrity and quality assurance. Detail-oriented with a proven track record in enhancing patient and customer satisfaction. Experienced in thriving within GMP environments, delivering consistent results.
Overview
9
9
years of professional experience
Work History
Quality Control Microbiology Tech II
Abbvie (Contract Actalent)
Worcester, Massachusetts
01.2026 - Current
Performed microbiological testing on raw materials and finished products to ensure compliance with quality standards.
Quality Control Specialist
Vertex Pharmaceuticals
Providence, USA
04.2023 - 08.2025
Drafted and implemented a global Invalid Data Analysis Procedure including and instructor-led training for all Quality Control labs.
Implemented new training process for Quality Control Final Medical Device Inspection as SME.
Participant of QP and Internal audits as a Quality Control Subject Matter Expert.
Lead Specialist for Quality Control Gap Assessment
Vertex in-house Lean Six Sigma Program White Belt
Represented the Quality Control group in various collaborative projects and meetings across local site and global projects .
CAPA, Quality Events, and NCMR (NCR) documentation
Raw material sampling and testing for medical device constituents using FTIR, DSC, Porosity, and Thickness measurements.
Ensured facility adhered to ISO 13485 regulations
ISO 22367 independent research
Qualified trainer for Gurley Densometer, Constituent sampling, and Final Device Visual Inspection
Quality Control Analyst
Resilience National (Contract Clinlab Staffing)
Marlborough, USA
01.2023 - 04.2023
Cross Contamination Risk Assessment/Analysis for a new facility using ICH guidelines.
Associate Research scientist, Microbiology center of excellence at Bristol-Myers Squibb CompanyAssociate Research scientist, Microbiology center of excellence at Bristol-Myers Squibb Company