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Jt- Associate Pilot Plant

Job in West Greenwich, Kent County, Rhode Island, 02817, USA
Listing for: Quality Consulting Group, LLC
Full Time position
Listed on 2026-02-06
Job specializations:
  • Science
    Clinical Research, Medical Science
Job Description & How to Apply Below
Position: JT932 - ASSOCIATE PILOT PLANT
Location: West Greenwich

Overview

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic individual to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities
  • Lead management of materials including oversight of sample requests, test submission, storage, and shipping coordination.
  • Support execution of cell culture and purification processes to include, but not limited to: aseptic processes, bioreactor operations, chromatography, and filtration
  • Perform additional routine tasks including, but not limited to:
    • In-process sampling
    • Operation of laboratory analyzers
    • Compounding media and buffer solutions
    • Clean-In-Place (CIP) and Steam-In-Place (SIP)
    • Equipment assembly and disassembly
    • Routine maintenance of benchtop analyzers
    • Escorting and providing oversight of vendors
    • General lab organization, cleaning, and inventory-related tasks
    • Utilize scientific principles in execution of experiments and analysis of experimental data
    • Carry out laboratory tasks per plan and procedure in a team environment
    • Document data and process information in accordance with good documentation practices
    • Perform laboratory safety evaluations
    • Perform minor equipment maintenance
    • Help maintain laboratory standards with a focus on safety, quality, and compliance
Qualifications
  • Bachelor's or associate degree in related area preferred
  • 1+ year of related experience
  • Prior hands-on experience in pilot- or large-scale 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
  • Well organized with excellent written and verbal communication skills
  • Ability to work fully onsite
  • Ability to support weekend work
  • Willingness to work hard, learn, and be self-motivated
  • Dayshift (start time and end time can be flexible)
  • Must have the ability to support WEEKEND work
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Position Requirements
10+ Years work experience
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