Quality Control Laboratory Technician 3

iTech

  • Newark, DE
  • Permanent
  • Full-time
  • 2 months ago
Position Overview /ResponsibilitiesThis is a six-months contract position. The technician will be responsible for activities related to manufacturing testing within the Quality Control Organization. Functions and responsibilities may include and are not limited to:
  • Completes analytical related testing/processes on analytical instruments such as Titrator, Karl Fisher, UV-VIS, Spectrophotometer and pH meter.
  • Completes manufacturing related testing/processes on Diagnostic equipment and analyzers such as, DM Vista, SCS Stratus, Centaur and Atellica analyzers.
  • Performs the most complex quantitative and qualitative analysis, such as sampling, testing, and measuring using analytical instruments and diagnostic analyzers.
  • Compiles, analyzes, and interprets large sets of test data.
  • Performs complex analysis of data and calculations in excel or LIMS which includes graphs and charts.
  • Enters data into internal software and generates documents as required.
  • Performs periodic inspections of equipment and preventative maintenance work.
  • Maintains instrument logs
  • Ability to follow protocol and schedules
  • Performs troubleshooting on issues that may arise during testing process.
  • Might be required to participate on cross functional teams as needed (scientists, engineers, and management).
  • Potential to work independently on projects which includes defining tasks, setting priorities, and driving to completion.
  • Flexible to work overtime and/or irregular work hours as needed.
  • Knowledge of QSR's and ISO standards.
  • May require participation in new product development, production support and/or reference materials.
  • May provide general guidance to others and train lower-level employees.
Knowledge/Skills and ExperienceKnowledge and skills of a technical or specialty area, with 3-5 years of experience including but not limited to the following:
  • Understands the quality management system and ensures that their area complies with FDA, QSR, ISO and IVDD standards.
  • Familiarity with GMP, GLP, and GDP processes
  • Mathematical skills: concentration calculations and statistical analysis.
  • Computer skills: customary MS Office programs, SAP, LIMS, and/or Siemens Clinical testing software.
  • Laboratory skills: operation, maintenance and troubleshooting of analytical instruments and chemistry assays.
  • Knowledge and experience with analytical instruments and testing methodologies are a must.
  • Demonstrates ability to work independently on a team and be able to multi-task and prioritize daily work.
  • Strong communication and interpersonal skills.
  • Knowledge and experience in handling bio-hazard materials.
Education
  • Bachelor's degree in a relevant science (e.g., chemistry, biology, biochemistry, 2-year degree with experience in Medical Diagnostics or equivalent)
  • Individuals with an associate degree may be considered, depending on candidate's prior job experience

iTech