Joseph F. Muratti
Sugarland, Texas ***** 254-***-**** *******.******.*@*****.***
Linkedin.com/in/Joseph-Muratti
Professional Summary
Versatile Chemist capable of working with different kind of chemicals, compounds and materials. Strong understanding of chemistry and laboratory principles. Understands the importance of teamwork with the ability to lead when necessary.
PROFESSIONAL EXPERIENCE
PHARMEDIUM, Sugarland, Texas September 2018 – April 2020
EPA Chemist
Responsible for the analysis of validation protocols, raw materials and finished products utilizing High Performance Liquid Chromatography (HPLC) and Ultrapure Liquid Chromatography (UPLC). Used Empower Software for the acquisition, processing and reviewing of data.
Regularly audited laboratory housekeeping to ensure neatness and compliance with Health, Safety, and company policies.
Maintained accurate notebook of all sample identification, raw data and calculations associated with assigned analysis duties and organize, performs and reports results of testing materials.
ALLERGAN, Waco, Texas August 2010 - April 2018
Laboratory Technician V
Assisted Chemistry Laboratory staff for the execution of validation protocols, raw materials, bulks, in-process, and finished products utilizing High Performance Liquid Chromatography (HPLC). Laboratory 5-S coordinator and responsible for organization and cleanliness of laboratory. Conducted bulk release in absence of professional.
Interfaced with QA counterparts to optimize laboratory support of QA and production activities.
Supported the laboratory maintaining a safe environment in accordance with safety standards.
Set up operating and troubleshot all laboratory instrumentation. Performed minor instrument repair.
CORDIS LLC, A J&J COMPANY, San Germán, Puerto Rico January 2003 - December 2008
QA Lab Senior Auditor, January 2006- December 2008
Served as Supervisor backup regarding management responsibilities, which included task assignment, lot approval, and preparation of schedules. Supported daily laboratory operations.
Reviewed analytical laboratory data for accuracy, completeness, legibility, and compliance with cGMP’s, Standard Operating Procedures (SOP’s), Laboratory Work Instructions (LWI’s), required specifications, and company policies.
Coordinated testing with Lab personnel to ensure promptly response.
Assisted in Laboratory Investigations.
QA Lab Senior Scientist, January 2003 – December 2005
Performed analytical testing for raw material, in-process and finished products that included the following: Drug Content Uniformity per USP <905>, Elution Testing per USP <711> and <724>, Residual Solvent Methods per USP <467> utilizing HPLC and Gas Chromatography (GC), Elution Testing Apparatus USP #4 and #7 UV-Spectrophotometry, Flame Spectroscopy (FAA), Graphite Furnace (GFAA), Mercury Analyzer, and Inductively Coupled Plasma (ICP).
Conducted wet chemistry analysis per current USP, Heavy Metals, Residue on Ignition, Polarimetry and Water Determination by Coulometric and Direct methods. Used Empower Software for the acquisition, processing and reviewing of data.
EDUCATION
Master of Science in Biology - Environmental Toxicology
University of North Texas, Denton, Texas
Bachelor of Science in Biology
Interamerican University, San Germán Campus, Puerto Rico
CERTIFICATION
Certified as Laboratory Information Management System Administrator
PROFESSIONAL DEVELOPMENT
Effective Handling of FDA Inspections
Training as Certified Quality Auditor
Biotechnology Industry Training Program