Joyce M. Green
973-***-**** / Email: ********@*****.***
Summary With over 18 plus years of laboratory experience in the pharmaceutical industry and healthcare diagnostics within research and development as well as stability and validation. Proficient in Microsoft office excel, word, power point and outlook working with robotic equipment such as tecan, TAP systems and RTS, detailed orientated, great with time sensitive projects and a self-starter. Training others and managing projects. Exceptional in dealing with customers on projects, solving issues and troubleshooting equipment and software issues.
Experience Siemens Healthcare Diagnostics Tarrytown, NY 1/2015-Present
Biochemist 2 for VSC - Validation / Stability / Compatibility Group working in Stability mainly
Provides support in a wide variety of semi-complex technical assignments conducting semi-complex tests or investigations pertaining to the development of new designs methods, materials, or processes and investigates possible application of results.
Responsibility include but not limited to; monitoring the entire life cycle of all the stability samples from receiving in the lab until the end of the study.
Obtains, correlates, and analyzes technical information needed to accomplish semi-complex tasks. Provides support in preparing and writing reports, charts, graphs calculating and records results, and often develops conclusion and other documents.
Contribute to the developing of designs for a variety of products, processes, and components working with ADVIA centuar placing assays on stabilities studies time sensitive test
Responsible for maintaining the equipment such as performing daily, weekly and monthly maintenance as needed and performing primes to insure that the equipment mechanisms are working properly. Insuring the systems maintain proper and accurate results by performing System Monitoring Testing (SMT).
Merck & Co., Inc. Corporation Rahway, NJ 5/1997-11/2013
Research Scientist for Compound Management in support of Drug Discovery
Initiate complete processes of compounds for Lead OP
Responsible for cherry pick from the Thermo RTS automation system and the Oscar TAP (The Automation Partnership) system through the Mosaic software to prepare custom plates and solid weighing for various research projects throughout drug discovery, plate making, and to replenish the micro tubes for RTS and Tap systems and set up for LCMS testing for the purity of the samples
Controlled, wrote new or rewrite existing scripts for the Tecan genesis for offline diluting and specialize plate preps and activate robotic equipment for solubilizing vials, micro tubes
Organizing research compounds for time sensitive project for external client locally and international
Preparing Sin Set collection of samples for mass testing from weighing to making and creating stock solution for storage
Assist others in ongoing projects such DMPK (Drug metabolism Pharmacokinetics), new compound acquisitions, QC, data base access requesting of samples, input of data stored and kept records of SOPs (standard operating procedures)
Handling shipping and receiving of compounds to and from the US and international
Maintain and sustain the equipment optimization of usage by calibrating, fixing broke tips and replacing, cleaning and getting PM (preventative maintains) is preformed every 6 months based on service contracts
Ordering supplies, talking to vendors and making sure the proper lab ware is available from disposal able tips, plates for specific projects and shipping materials.
Confer with chemist and biologists to determine specific premasters tailored to meet their testing requirements, helped with testing database to allow them t place orders or their compounds
Worked in -4 degrees freezers for plate storage and sample storage conditions and working with hazardous materials through safety
Meadox Medical Incorporated Oakland, NJ 10/1996-4/1997
Responsible for the retention or release of medical grafting samples
Tested and approved textiles through physical testing (pH, UV-Vis Spec, etc)
Delegated whether or not products should be tested after production
Calculated results to determine whether to retain or to release product
Heat testing of the graft through visual inspection ensuring the product meets specified requirement
Inspecting work area to insure cleanliness, safe and meet FDA standards
Skills
OSHA/GLP, Tecan Genesis 100,150,200 & Evo, Centrifuge, pH meter, multi-pipette head, Microsoft excel, Word & Power Point, Outlook, RTS Automation, TAP system, Calibrations, Six sigma certified, ADVIA Centuar
Education Rutgers University
360 Martin Luther King Jr. Blvd
Newark, New Jersey 07102
Currently Attending
Essex County College
303 University Avenue
Newark, NJ 07102
Graduated: May 2005
AAS Chemical Technology
Certified 1994: Laboratory Technician (TTP)