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Click here or scroll down to respond to this candidateCandidate's Name
Franklin Park, New JerseyTelephone: PHONE NUMBER AVAILABLEEmail: EMAIL AVAILABLESeeking an opportunity, where my education, advanced scientific knowledge, and technical skills and my experience can be utilized and become a prominent asset for employer as a medical biller.TECHNICAL EXPERIENCE SUMMARY15 years of Scientific, Technical experience with a proven record of success in the Manufacturing, Process Development, External Manufacturing, Technology Transfers, Site Transfers, Technical Documentation, for Oral Solids and Liquids, Proficient in Processing and Handling of Potent Compounds and Controlled Substances (Class II & III)In-depth knowledge of processing full-cycle billing and charge entry for all types of claimsPayment postings, claim follow up, preauthorizations and EOBs.Basic healthcare coding and electronic medical recordsFamiliar with interviewing, selecting, and evaluating performance of all direct billing reports.Knowledge of medical and billing terminology.CLINICAL EXPERIENCEComplete Foot and Ankle Specialists, New Jersey Feb 2024-March 2024Medical Billing Internship Rotation- 80 hoursPosted claims, performed eligibility of claims.Updated demographics, scribing, and reviewed all patient data to update in EHR.Scanned documents to patient charts, received calls and scheduled appointments.Assisted with new patient information.Abided by all HIPAA guidelines.WORK HISTORYAPPCO Pharma LLC, New Jersey, USA Jan 2020 to April 2023Production / Warehouse Supervisor, (Manufacturing, Technology Transfers, External Manufacturing-CMO)Effectively communicates with Senior Management, Internal (Supply Chain, Production, Quality Control, & Business Development), External Stakeholders of Global sites, and CMO / CDMO point of contacts to promote positive and collaborative relationships between the stakeholders.Execute Commercial manufacturing batches, robust Technology Transfers., per project timelines.Well versed initiating, reviewing, and approving the CAPAs, Investigations, and cGMP Technical ReportsSuccessfully completed, submitted the multiple FTF (NCE-1), NDA projects. Familiar with the principles ofWell versed with CAPEX and yearly project budget management, regularly communicates with Supply Chain / Procurement for long-term forecasts and initiates Purchase requisitions to ensure the materials are delivered on time.Receiving RM and PM following SOPs and shipping Finished Products to different clients.MSN Pharmaceuticals Inc., New Jersey, USA Sept 2017 to Jan 2020Senior Process Development Scientist, (Exhibit Batches, Technology Transfers, External Manufacturing-CMO)Leads Technology Transfers from Global R&D Sites to ensure the successful transfer of Optimized Final formulations, Transfer of Analytical methods.Well versed initiating, reviewing, and approving the CAPAs, Investigations in Track wise.Successfully completed, submitted the multiple FTF (NCE-1), NDA projects. Provides the technical Reports, documentation, CMC elements for regulatory filings and responses to FDA Deficiencies within the stipulated period.Well versed with Formulation Development activities, such as Literature Search, Patent search, Journals, Orange book, Brand and Generics, Physio-chemical properties, Stability, Pharmacokinetics, Chemical Abstracts,Well versed with SAP transactions, updating GRN for API Indent/Procurement (DMF source)Drafted, reviewed, and approved the SOPs for the equipment and other procedures.Involved in purchasing all industrial equipment and Raw MaterialsWell communication with different vendors for price comparison and choose the right cost-effective materials for commercial batches.Novel Laboratories Inc. /Lupin, New Jersey, USA Feb 2007 to Sept 2017Formulation Scientist, Manufacturing Group Leader (Formulation, Exhibit Batches, Technology Transfers)Successfully developed and commercialized the Calcium channel blockers, Proton pump inhibitors (PPIs) Sustained and Extended-Release solid dosage forms. Completed Technology Transfers and Process Validations for Oral Solid Dosage forms of Generic Rx products.Individual to inspire trust, to embrace sense of ownership and orchestrate multiple, concurrent requirements to deliver projects at cost and on time. Managed multiple direct and indirect reports, responsible for the Pilot (Solid Orals) plant.Involved in sourcing of DMF grade APIs and excipients, involved with manufacturing and analytical departments for rectifying and troubleshooting various issues.Wrote, Reviewed and approved cGMP documentation (BMRs, Investigations, SOPs, Protocols and Reports) and involved in IQ, PQ and OQ qualifications for R&D Pilot plant equipment.Involved in HPLC assay testing methods for impurities.Bridgeport Chemists Inc., CT, USA Feb 2005 to Feb 2007Pharmacy TechnicianWell versed with Medications Dispensing as per the prescriptionsCommunicating with patients, nurses and Physician officesData entry of patient profiles, Filling out refillsScheduling pickups and deliveries of medications.EDUCATIONMedical Billing and Coding Certificate AIMS Education, Edison, NJ (2023-2024)Master of Pharmacy- J.S.S College of Pharmacy, Dr M.G.R University, INDIABachelor of Pharmacy- V.L College of Pharmacy, Gulbarga University, INDIAComputer Skills: - MS Office, SAP (Transactions in Material Management) |
