JT653 - 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:

Following Good Manufacturing Practices (GMPs) and applicable regulations from the Code of Federal Regulations (CFRs).
Reporting any discrepancies to the Team Leader or Production Supervisor to ensure quality standards and safety.
Ensuring quality & compliance through a Right First-Time mentality.
Receiving and preparing components for use in manufacturing.
Feeding components into equipment and performing sanitation activities.
Documenting appropriate paperwork, understanding Overall Equipment Effectiveness (OEE)/performance metrics, and participating in daily performance meetings.
Use of pallet jacks (Manual and Powered) to move equipment and buffer totes.
Use of computer systems to support material inventory and electronic batch record management.
Partnering with cross-functional teams to drive improvement opportunities.
Ensuring components and products are available for continuous operation.
Set up and operate downstream equipment for the purification process.
Cleaning, prepping, and processing for chromatography, Viral Inactivation/Neutralization, Viral Filtration, Tangential Flow Filtration and Final Filtration and Fill.
Use of single use and stainless-steel equipment.

Qualifications:

Bachelor’s degree in related area
No experience required (Preferably Biotechnology and GMP background)
Strong work ethic and desire to learn new skills
Strong public speaking and technical writing skills
This role will specifically be to support B-shift rotation.
Swing shift consists of 2 working days during Week 1, and 5 working days during Week 2, starting at 6:30am – 7:00pm
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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