JT306 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN NS

West Greenwich, RI

Temporary

Biopharmaceutical

Entry Level

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.

Responsibilities:

Hands-on operations: set-up, operation, and sanitization of various manufacturing equipment
Operate or comfortable learning to operate electric pallet jack
Performing parts washing and sterilization activities
Weighing out buffers/media per procedures.
Maintaining an organized and clean workspace
Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
Initiating and being involved quality deviation reports, as required
Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
Using computer systems, performing and monitoring critical processes with the ability to perform basic troubleshooting
Performing in-process sampling of drug substance and operating analytical equipment (pH meters, conductivity meters, BGAs, etc.)

Qualifications:

High school/GED + 1 year of work or military experience or Associate degree
Understands the principles of safety culture and working with integrity
Ability to read and follow Standard Operating Procedures.
Ability to work in small teams or pairs.
Flexibility in the work environment.
Nice to have: mechanical skills, manufacturing exposure, single use technologies, sampling methods and procedures experience.
Strong eagerness to learn and shows a sense of ownership in their work or experiences
Open to candidates that don't necessarily have experience in Biotech cross lateral could be anything with batch chemicals or chemical processing.
Candidates must be available to work weekends and holidays.
Night shift with a rotating schedule every two weeks:
Week 1: Wednesday & Thursday, 7:00 PM - 7:00 AM
Week 2: Monday, Tuesday, Friday, Saturday, Sunday, 7:00 PM - 7:00 AM

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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