Microsoft Outlook, Word, Excel, Internet Explorer, MARC (Warehouse Management System), Compliance wire (Learning Management System), Documentum (Document Management System), Kronos (time attendance system).
Extensive training in GMP, environmental, health, safety, industrial vehicles, DOT, IATA, and leadership development. IMPETUS SYSTEMS & CAREERS, North Brunswick, NJ - CBCS- Certified Billing & Coding Specialist.
CAREER DEVELOPMENT SKILLS:
Medical Terminology & Human Anatomy
Medical Coding, Billing activity and follow up for receivables on Medicaid/Medicare claims, other private insurance carriers such as BCBS, Aetna, Cigna ECT.
Knowledge of paper-electronic document conversion process (Medical/Healthcare industry) Microsoft Office tools (MS Word, Excel, Power Point)
Maintains a GMP receiving, labeling, material movement, shipping, cleaning materials, and kitting for manufacturing process as required.
Maintains a cycle-counting & physical inventory process to ensure inventory accuracy and availability of product to support production.
Handles returns to suppliers and resolves issues with procurement.
Knowledge of handling temperature sensitive products including receiving, storage, labeling and packaging.
Self-motivated and detail-oriented with absolute adherence to all related procedures.
Able to perform all material management functions within a cGMP warehouse environment including lifting (up to 50 lbs) Ability to learn and adapt to new procedures and technology Handling of blood product to support operations.
Johnson & Johnson JOM Pharmaceutical Services, Inc- Bridgewater, NJ.
1998-2008 Warehouse operator Member of self-directed team responsible for executing all warehouse functions to achieve accurate and on time delivery of ambient, temperature controlled products.
Possesses extensive system knowledge including MARC (warehouse inventory &order management system) Microsoft office (Word, Excel), Compliance Wire (Training database), SAP system.
Required knowledge and understanding of bar codes, product coding, temperature restrictions and modes of transportation to meet the variety of delivery requirements.
Posses dynamic team skills and received extensive training in intrinsic motivational skills, giving & receiving feedback, setting and monitoring performance & business in enabling performance within a organization that relied on self directed teams.
Key team member of Safety Team and First Response team.
Knowledge on GMP, HAZMAT, OSHA, DEA, and ISO-14001 regulations governing the distribution operation as well as the internal procedures that ensure pharmaceutical handling enables track and trace capabilities.
cycle count procedure).
QC Inspector February 2013 to CurrentLifecell Corporation － New Jersey
Responsible for performing Quality Control functions including receiving and in processing inspections, reporting of non-conforming materials, transfer of released components, and discard of rejected goods.
Provide additional technical support for the Quality Control Department to ensure effective operations.
Maintain database and history files for components and subassemblies.
Perform label and package inspections and maintain Quality Control quarantine areas.
Coordinates shipments of test samples to outside contractors.
Follow SOPs to perform Quality Control inspections.
Maintain receiving, inspection and transfer records.
Ensure appropriate levels of supplies and equipment.
Maintain appropriate databases.
Perform label and package inspections.
QA Inspector August 2012 to October 2012Padtech － Flemington, New Jersey
Maintain the QC inspection areas in an orderly fashion conducive to carrying out safe and efficient inspections and procedures.
All instruments and equipment will be maintained in optimum and calibrated condition so that results are accurate and reproducible.
Maintain records of inspection and all testing performed on the appropriate test records Identify and implement opportunities for continuous improvement, including document revisions in order to maintain accurate SOPs.
Perform line clearances in manufacturing and other quality reviews during manufacturing activities Perform inspections off site Perform all other related duties including special projects.
Warehouse Operator September 2010 to August 2012Ortho Clinical Diagnostic － Raritan, New Jersey
QA Inspector responsible for performing line clearance activities in manufacturing and packaging areas.* These activities include; a) verification that all previous materials and/or products have been removed from the area/line, b) all required cleaning has been completed by verification of entries in appropriate logs, and c) that equipment has been set up per SOP instruction and/or as directed in the batch record.
Collect samples and performing testing and/*or inspection as directed by SOPs and/or the Batch Record.
Responsible for documenting activities as required by the batch record and/or SOP and for performing such documentation on an immediate basis.
Responsible for adhering to all applicable written procedures as well as the requirements of current Good Manufacturing Practice (cGMP) Responsible for performing designated verifications assuring the processes are being performed as required by applicable written documents ( SOPs, batch record, protocols, etc.) Responsible for performing sampling and inspection functions for raw materials and packaging components.
Billing, c, continuous improvement, conversion, CPT, databases, database, Document Management, documentation, Documentum, fashion, GMP, Good Manufacturing Practice, ICD-9, instruction, insurance, Internet Explorer, Kronos, leadership development, materials, Medical Billing, Medical Terminology, Medisoft, Excel, Microsoft Office, Microsoft Outlook, Power Point, Word, MS Word, packaging, policies, processes, Coding, protocols, quality, QA, Quality Control, receiving, reporting, safety, SOP, technical support, written
Member of team awarded the Cardinal Supplier Quality Award for meeting customer requirements.
Compania de Maria, Flores Tovar Bogota-Colombia