Objective
To obtain a position where my skills and experience can be utilized towards establishing a productive work relationship.
Education
High School: Hunterdon Central Regional High, Flemington, NJ Graduated, 2007
Dover Business College Dover, NJ Graduated 2011-2012 Major: Medical Assistant
Work Experience
Roche Diagnostics
Branchburg, NJ
Diagnostic Technician Associate Oct 2018-Present
Perform visual inspection of components produced in the filling area prior to place them into the Finish good kits to ensure products are free of defects and have met the required acceptance criteria
Pack filled vials, inserts and barcode clips into finish good totes and Kits according to approved standard operating procedures and Production Batch Records.
Perform Reconciliation of components and intermediates labels, inserts and other components associated with the products being packed and transfer final packages to the appropriate storage locations.
Responsible for ensuring all operations are carried out according to cGMP, SOPs and OSHA requirements
Center for Educational Advancement Flemington, NJ
Special Aid assistance teacher March 2018– Sep 2018
Provide one to one assistance to the special aids students.
Mentor and help solve problem and quickly deal with a variety of issues with students.
Counseled youth regarding job placement
Influence the minds and lives of student to help growth and development
Assist in school trips to library and various places
Ortho Clinical Diagnostics
Raritan, NJ March2017-March 2018
Manufacturing Operator
Responsible as a team member to pack 170 different Finished Good SKU’s
As a team member, responsible for inspection of various product put-ups to ensure products are free of defects and have met the required accepted criteria
Performed line set-up/clearance according to approved standard operating procedures
Responsible for ensuring all operations are carried out according to cGMP, SOPs and OSHA requirements
Created various bulk orders for different departments in CAMA (BioVue, Antisera, MTS GEL)
Signed off on each batch record created for bulks provided on every Spider Work Order
Required calculations of each specific chemicals to be put into each bulk created
Assigned to print out and add lot numbers for every batch record needed per week
Ortho Clinical Diagnostics June 2016-Dec 2016
Raritan, NJ
Document Control Specialist
Processed validation forms
Created/updated validation numbers in Validation Database
Closed off validations
Scanned/Uploaded projects into OTIS
Archived all current/closed projects off to Iron Mountain
Created master folders
Worked on Micro-Clean files
Scanned RBMF files into OTIS
Tiffany and Company Oct 2013 – Jan 2014
East Hanover, NJ Outbound Processor
Perform and executed packaging operation according to standard operating procedure
Knowledge of cGMP requirements
Inspect and verification process
Performed packing process for China lot
Initiated and red lined SOP’s, batch records and routed for approval
Hunterdon Family Practice & Obstetrics April 2012 – May 2012 Raritan, NJ
Intern Medical Assistant
Performs and input patient vitals
Assist patient to the exam room
Performed the Anthropometrics (height, weight, BMI) for the patient
Performed room cleaning and set up
Performed Urinalysis and Venipuncture
Performed Centrifuge blood
Performed Mammography
Performed Health history, Social history
Sent out Rx orders, faxed paper work
Pulled and prepared patient chart
Performed instrument sterilization set up
Performed set up sterile field for procedures
Performed suture removal
Assures quality of products by performing a visual inspection of product and components
Janssen Pharmaceuticals May 2010 – Nov 2010 Raritan, New Jersey
Documentation Specialist
Execute Change Control process to update documents
Initiated and red lined SOP’s, batch records and routed for approval
Organized terminated representative files
Put paperwork into piles from past to present
Archive files/paperwork and sent to Iron Mountain
Past paperwork was discarded
Ortho Clinical Diagnostics March 2008 -June 2008 Raritan, NJ
Quality Control Inspector
Performed incoming inspection and release of approved labels.
Verify and document inspection results per specification.
Accurately complete documentation in batch records, forms and other GMP documents.
Demonstrate training progression through assigned curriculum.
Knowledge of cGMP requirements to ensure adherence to compliance policies and regulations.
Execute change control process to update documents.
Revised documents by red lining and routing for approval
Computer Skills: Windows 7 (MS Word, PowerPoint, Excel).
Certification
CPR-certified 2011 EKG-certified-2011 CCMA-Certified-2012