JT886 - ASSOCIATE PILOT PLANT

Quality Consulting Group•West Greenwich, RI

9d•Onsite

About The Position

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic 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.

Requirements

Bachelor’s degree in Engineering or Science (Preferred not required)
Relevant hands-on laboratory/manufacturing experience.
Demonstrated problem-solving ability and strong attention to detail
Excellent written and verbal communication skills

Nice To Haves

Internship or co-op experience is preferred.
Academic laboratory experience is acceptable.
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

Responsibilities

Support execution of cell culture processes, including: Aseptic vial thawing, Cell culture flask passaging in biosafety cabinets and Operation of benchtop wave bioreactors and 200L & 500L single-use bioreactors.
Support large-scale harvest and downstream purification operations, including: Chromatography, Filtration and Ultra-Filtration/Diafiltration (UF/DF) using pilot-scale skids and equipment.
Perform routine laboratory tasks, including: In-process sampling, Operation of laboratory analyzers, Sample management, Scientific data collection using electronic laboratory notebooks (ELN), Media and buffer compounding and Clean-In-Place (CIP) and Steam-In-Place (SIP).
Equipment assembly and disassembly
Routine maintenance of benchtop analyzers
Vendor escorting and oversight
General lab organization, cleaning, and inventory management
Utilize scientific principles to execute experiments and analyze data
Perform laboratory work according to plans and procedures in a team environment
Document data and process information in accordance with Good Documentation Practices (GDP)
Perform laboratory safety evaluations
Conduct minor equipment maintenance
Maintain laboratory standards with focus on safety, quality, and compliance