JT818 - 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:

Support Downstream Manufacturing Operations
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.
Drafting and revising documents (SOPs, MPs)
Performing in-process sampling of equipment and operating analytical equipment
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)

Qualifications:

Bachelor's degree preferred or associate degree.
3 years work experience in manufacturing.
Manufacturing experience in a technical field/ manufacturing associate would be the equivalent for this role.
Experience in a technical field
Experience with advance computer systems
Demonstrated ability to follow procedures
Swing shift that consists of 2 working days during Week 1, and 5 working days during Week 2.
Candidates must be available to work weekends and holidays.
Shift Times will be: Start time 6:30 AM - 7:00 PM
Available to work various shifts (day/nights) as dictated by the production schedule Able to work in teams to complete operational tasks

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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