JT880 - MANUFACTURING PROCESS TECHNICIAN

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, cleaning, and sanitization of various manufacturing equipment
Weighing out buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
Performing and monitoring critical processes with the ability to perform basic troubleshooting
Initiating and being involved quality deviation reports, as required
Perform Raw Material weighing.
This is a manual task involving physically scooping materials from a barrel into a bag.
Solution batching: candidate will make 5000L solution batches of Medias and Buffers to be used in Upstream or downstream process using single use bags and tubing.
Perform analytics such as pH, Conductivity, and Osmolality on the solutions they are batching
Utilize Werum/MES as well as DeltaV Automation to perform weighs and batching
Move large metal containers using an electric pallet jack.
Perform single use inspections of materials before use to ensure they are fit for use.

Qualifications:

Bachelors OR High school with 3 years work experience in manufacturing.
Ability to follow Standard Operating Procedure (SOP)
Good written communication, experience working in a team not direct manufacturing experience understands the principles of safety culture and working effectively on a team, lab exposure and worked in an environment where safety is top priority.
Experience in Biotech cross lateral or could be anything with batch chemicals or chemical processing
Day Shift 6:45AM - 6:45PM
A and B Rotation - Swing Shift - Week 1 is 5 working days Week 2 is 2 working days.
Candidates must be available to work weekends and holidays.

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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