Biotechnician practicing Quality Assurance & Manufacturing in Nuclear Pharmaceuticals, Aerospace, Aviation Lamination, and Food & Drug Sciences in the State of New Jersey since 2013.
Overview
13
13
years of professional experience
Work History
Nuclear Pharmacy Technician
Siemens Healthineers
Hackensack, NJ
07.2025 - Current
Manufacturing complex FDG and Biomarker compounding with cyclotron and chemistry module operations.
Adhering to quality control processes utilizing analytical equipment TLC, HPLC, GC with ISO 1 & 5 sterile procedures under supervision as required by State and Federal law.
Participate in Federal FDA, state and vendor inspections, equipment maintenance and troubleshooting to support manufacturing and testing processes collaborating with 24/7 Tech Support.
Implement approved SOP changes to production and quality control processes
Oversee routine logistics functions including preparing product for shipment, coordinating courier schedules, and documenting as necessary.
Prepare and dispensed radiopharmaceuticals following strict safety protocols and regulatory standards.
Collaborated with healthcare professionals to ensure accurate medication delivery and patient care.
Operated specialized pharmacy equipment for compounding, labeling, and storing radioactive materials.
Maintained inventory management systems to track stock levels and optimize supply chain efficiency.
QC Analyst II
LANXESS Specialty Chemicals
East Hanover, NJ
03.2024 - 06.2025
Aviation Oil Distribution | Quality Manufacturing
QC development, manufacturing chemical intermediates, additives, specialty chemicals.
Ensured accurate, accurate data production while adhering to Quality Control Lab Technician training procedures, ISO 9001 standards, and aerospace oil production and quality control analysis codes.
Communicated and documented results effectively and in a timely manner, both verbally and in writing.
Supported company safety initiatives by participating in safety programs and meetings.
Conducted testing on and approved incoming raw materials, in-process samples, and completed production batches.
Performed testing on outgoing samples (containers, tank wagons, drums, totes) from Traffic and Warehouse.
Tested R&D and other sample types for quality and compliance.
Recorded test results accurately in workbooks, testing plans, LIMS, and SAP systems.
Reported unsafe conditions, out-of-spec results, or unsafe behavior to supervisors promptly.
Adhered to Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Documentation Practice
QA Manufacturing Operator
Lamart Corporation
Clifton, NJ
06.2020 - 10.2024
Manufacturing Technology: Cat-bridge Systems | Quality Manufacturing
Manufactured Pressure-sensitive adhesive products for Aerospace Technology
Operating and Maintaining an Industrial Cat bridge System.
Establishing Quality Safety and Culture within the Operations, manufacturing, Supply Chain, Warehouse, and QC Matrix by identifying Variables, Material Attributes, and Critical Process Parameters.
Support Compliant Quality Procedures in the QMS, Development, and Engineering Divisions.
Assisted in QC Wet-Lab to determine product stability and QA utilizing tensile analytical technologies.
Adhered to Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Documentation Practice
QC – QA Senior Laboratory Technician
Spectro | Jet-Care
Cedar Knolls, NJ
01.2015 - 05.2022
Conducted bioanalytical testing in support of Petroleum-based Jet fuel and Oil analysis utilizing Complex Lab Technologies
Supported the Quality Management Team in Laboratory Investigation Reports, Quality Deviation Reports and Data Discrepancies throughout the QMS systems.
Adhering to NAS, AS, SAE, ASTM, FAA Regulatory Compliance.
Assessed CAPA - Root Cause analyses in compliance reviews to implement effective strategies for continuous improvement training in cross functioning departments.
Managed reagent and lab equipment for assigned areas of analysis and calibration.
Adhered to Laboratory Safety Standards, Installed and performed daily Calibration, Troubleshooting, Maintenance, startup and shutdowns.
Conducted training and supervision to junior lab technicians performing complex laboratory procedures and analyses.
Ensured that project scopes were completed within established deadlines.
Adhered to Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Documentation Practice
QC Laboratory Supervisor
Lab Express International
Fairfield, NJ
03.2013 - 09.2015
Pharmaceutical Quality Control Inspector for Biopharmaceutical grade Raw Material in the Manufacturing division.
QA | QC Laboratory Analysis - documentation proficiency resulting in the successful delivery of high-quality products within project scope timelines.
Wet Chem in ISO Airstream Class II Biosafety Cabinet Prioritizing Product Stability, formulation of media cultures, and Safety Standards in compliance with FDA, OSHA, and EPA.
Collaborated and assisted with product development
Adhered to Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Documentation Practice