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Quality Control Data Coordinator resume example with 5+ years of experience

Jessica Claire
  • Montgomery Street, San Francisco, CA 94105 609 Johnson Ave., 49204, Tulsa, OK
  • H: (555) 432-1000
  • C:
  • resumesample@example.com
  • Date of Birth:
  • India:
  • :
  • single:
Summary
  • Objective: To build a long-term career utilizing my 8+ years of experience in healthcare and 3+ years in clinical research, with an educational background in biology/chemistry. To obtain employment with a company that offers a positive atmosphere to learn and implement new skills and technologies for the betterment of the organization. Major Strengths
Skills
  • Skills in communication, time management for deadlines, detail oriented, work well under pressure.
  • Skilled in handling multiple projects within deadlines
  • Ability to prioritize multiple tasks and responsibility
  • Interdisciplinary Team Collaboration
  • Professional and matured attitude to maintain confidentiality
  • ART, Written
  • Aseptic techniques
  • Calibration
  • Clinical research
  • Database
  • Detail oriented
  • Experiments
  • Forecasting
  • Good laboratory practices
  • Inventory Management
  • Meetings
  • Monitors
  • Oncology
  • Procurement
  • Protocols
  • Quality assurance
  • Quality control
  • Research
  • Safety
  • Sample collection
  • SAP
  • Shipping
  • Time management
  • Troubleshooting
  • Data quality control
  • Reviewing data quality
  • Knowledgeable of quality control standards
  • Research and Data Analysis
Experience
Quality Control Data Coordinator, 03/2020 - Current
Thermo Fisher Scientific Inc. Rancho Cordova, CA,
  • Sample coordination and receipt from other departments for internal and external testing.
  • Assist in preparing of samples for shipment to contract laboratories.
  • Ensure that suitable written records and work undertaken are kept in accord with cGMP and company procedures.
  • Ensure adequate stock of aliquoting supplies through forecasting of upcoming sample submission.
  • Assist with maintaining inventory of QC non-critical and critical reagents as necessary.
  • Assist in creating and implementing Data Migrations Systems and Inventory Management Systems.
  • Assist with tracking sample receipt and chain of custody for internal and contract laboratory submission.
  • Perform QC document archival activities (i.e.
  • Submission and requests to Document Control department.
  • Worked closely with team members to deliver project requirements, develop solutions and meet deadlines.
Lead Lab Coordinator, 10/2018 - 03/2020
Johns Hopkins University City, STATE,
  • Flow Cytometry Immune Processing Core, Achieved in managing the internal review process for Oncology departmental research studies at Johns Hopkins University.
  • Adhered to positive and good laboratory practices; aseptic techniques pertaining to the collection, analysis, and processing of blood, urine, and tissue specimen.
  • Documenting, storing, and shipping of patients' specimens in accord with Study Protocols and manage temperature/liquid nitrogen (LN2) level monitoring.
  • Organize and maintain freezer inventory; keep track of due dates for batch shipment of specimens; and perform internal transfers of specimens to labs within the Cancer Center.
  • Attend clinical trial startup meetings and provide input for clinical research staff in regard to sample procurement.
  • Reviewed new trials and create correlative worksheets; oversee, train and monitors technical staff to ensure they follow established procedures or protocols, complete troubleshooting of samples that came to the lab with missing information.
  • Develop, review, revise, or approve SOPs along with experience in following IRB regulatory protocols.
  • Participates in the development and implementation of lab goals, objectives and development of PK sheets (study timelines).
  • Maintains excellent working knowledge of all assigned study protocols and reporting requirements.
  • Maintained all lab equipment (installation, operate, calibrate) and calibration binder, and ensured that all centrifuges, freezers, and pipettes are calibrated in accord with the schedule.
  • Active participation in safety programs, along with the ability to work safely and maintain a clean and orderly lab environment.
  • Maintain inventory of reagents and supplies through SAP systems.
  • Completed duties assigned by the Core Director or Core Manager with 100% accuracy.
Andrologist, 04/2018 - 09/2019
Shady Grove Fertility City, STATE,
  • Examines and processes specimens for routine semen analysis.
  • Perform counts for concentration and motility.
  • Perform histological techniques for identifying leucocytes, immature germ cells and morphology.
  • Processes semen for ART procedures and intrauterine inseminations (IUIs).
  • Recovery of motile sperm from normospermic specimens using selective methods (i.e., density gradient) should yield at least 10% of the initial motile sperm population, and increase the motility of the specimen post wash by greater than or equal to 10%.
  • Performs semen cryopreservation.
  • Performs testing for immunological infertility caused by antibody coating of sperm.
  • Performs sperm function tests offered by andrology lab including sperm survival.
  • Refers specimens to outside laboratories for semen culture when required.
  • Assures proper sample collection, delivery and identification.
  • Performs safe handling of specimens by following the safety guidelines for biohazardous, infectious and toxic substances in the andrology and IVF laboratories.
  • Performs daily/monthly quality control procedures for media and equipment used in the andrology laboratory.
  • Documents quality assurance activities including assessment of problems and appropriate corrective action.
  • Assists laboratory personnel in performing lab services in accordance with Federal, State, and local laws and guidelines to ensure laboratory maintains accreditation.
  • Assists as required in maintaining lab operations in conformity with the most current OSHA and CLIA regulations.
Lab Coordinator, 04/2016 - 10/2018
Johns Hopkins University City, STATE,
  • Flow Cytometry Immune Processing Core, Process/prepare human peripheral blood mononuclear cells (PBMC) using Ficoll gradient.
  • Follow good laboratory practices and collect, practice good documention guidelines.
  • Followed laboratory guidelines for handling biological specimens.
  • Cryopreserve processed sample using controlled freezer.
  • Experience with following IRB regulatory protocols.
  • Develops, reviews, revises, or approves SOPs, help organize and maintain freezer inventory.
  • Store new samples in liquid nitrogen, update database, retrieve samples with proper authorization and upkeep sample and database inventory; monitor overall sample inventory.
  • Perform internal transfers of specimens to labs within the cancer research center.
  • Attend clinical trial startup meetings and provide input for clinical research staff regarding sample procurement.
  • Planning for and implementing improvement programs in our research lab.
  • Provided total assistance for improving efficiency and output of laboratory experiments.
  • Point of contact for doctors, nurses, and study coordinators.
  • Managed departmental inventory and supply ordering through SAP Systems.
Education and Training
B.S: Biology, Chemistry, Expected in 2011
-
Coppin State University - Baltimore, MD
GPA:
: , Expected in 2005
-
Paul Laurence Dunbar High School for Health Professions - Baltimore, MD
GPA:
Activities and Honors

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Resume Overview

School Attended

  • Coppin State University
  • Paul Laurence Dunbar High School for Health Professions

Job Titles Held:

  • Quality Control Data Coordinator
  • Lead Lab Coordinator
  • Andrologist
  • Lab Coordinator

Degrees

  • B.S

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