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Jt- Associate Pilot Plant
Job in
West Greenwich, Kent County, Rhode Island, 02817, USA
Listed on 2026-02-06
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
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
- 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
Position Requirements
10+ Years
work experience
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