Manufacturing Associate (Cell culture) at Randstad Life Sciences US in West Greenwich, Rhode Island

Posted in Other about 19 hours ago.

Type: full-time





Job Description:

Title: Associate Pilot Plant/ Plant Manufacturing Associate

Contract: 2 Year

Location: West Greenwich, RI - 02817

Max PR: $26 - 31/hr

Job Description
  • Supports the execution of cell culture process to include, not limited to; aseptic vial thaw & cell culture flask passaging in biosafety cabinet through benchtop wave bioreactors & 200L & 500L single use bioreactors.
  • In addition, may support large scale harvest operations through downstream purification to include, but not limited to; chromatography, filtration, as well as, Ultra-Filtration/Dia-filtration (UF/DF) using various Pilot Scale skids & equipment.
  • Furthermore, may perform additional routine tasks to include, but not limited to; in process sampling, operation of laboratory analyzers, management of samples, scientific data collection via electronic laboratory notebook(s), compounding media/buffer solutions, Clean-In-Place (CIP), Steam-In-Place (SIP), equipment assembly & disassembly, routine maintenance of benchtop analyzers, escort & provide oversight of vendors, as well as, general lab organization & cleaning.
  • Utilizes scientific principles in execution of experiments & analysis of experimental data.
  • Carries out laboratory tasks per plan & procedure in a team environment.
  • Documents data & process information in accordance with good documentation practices.
  • Performs laboratory safety evaluations. Performs minor equipment maintenance.
  • Helps maintain laboratory standards with a focus on safety, quality, and compliance.

Basic Qualifications:
  • Bachelor's Degree in Engineering or Science OR Associates degree and 1 year of experience in laboratory or manufacturing setting OR 2+ years of experience in laboratory or manufacturing setting AND Ability to work weekends

Preferred Qualifications:
  • Prior hands-on experience in pilot or largescale cell culture or downstream purification process development or manufacturing.
  • Experience with automated computer controlled biopharmaceutical equipment.
  • Knowledge of process data compilation and analysis.
  • Demonstrated problem-solving capabilities and excellent attention to detail.
  • Excellent written and verbal communication skills

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