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Manufacturing Process Technician

Job in West Greenwich, Kent County, Rhode Island, 02817, USA
Listing for: Astrix
Full Time position
Listed on 2026-03-08
Job specializations:
  • Manufacturing / Production
    Manufacturing Production, Manufacturing Operations / Plant Manager, Operations Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 23.66 - 29 USD Hourly USD 23.66 29.00 HOUR
Job Description & How to Apply Below
Location: West Greenwich

Pay Rate Low: 20 | Pay Rate High: 29

We are seeking a Manufacturing Process Technician for our client, a renowned leader in biotechnology who is revolutionizing the use of living cells to create groundbreaking biologics. The ideal candidate will have 1–2 years of experience in a manufacturing or inventory environment and be comfortable working in a fast-paced, regulated production setting. This role requires flexibility to work a rotating 12-hour shift schedule and a strong commitment to quality, safety, and compliance.

Type: Contract

Location: West Greenwich, RI

Shift: 12-hour rotating schedule - day shift & night shift available

Dayshift Pay: $20 - $23.66/hr

Night shift Max Pay: $23.66/hr - $29/hr

Responsibilities
  • Follow Good Manufacturing Practices (GMPs) and applicable FDA regulations (CFRs).
  • Perform manufacturing operations in accordance with Standard Operating Procedures (SOPs).
  • Receive, prepare, and stage components for manufacturing use.
  • Feed components into equipment and perform required sanitation activities.
  • Use pallet jacks and manually wrap pallets as needed.
  • Utilize computer systems to support material inventory and electronic batch records.
  • Accurately complete and maintain required production documentation.
  • Monitor equipment performance and understand Overall Equipment Effectiveness (OEE) metrics.
  • Participate in daily performance meetings and continuous improvement initiatives.
  • Identify, troubleshoot, and elevate issues to the Team Leader or Production Supervisor.
  • Assist with basic troubleshooting and review of documentation.
  • Maintain an organized, inspection-ready work environment.
  • Support CAPA and Continuous Improvement activities.
  • Collaborate with cross‑functional teams to ensure materials and products are available for continuous production.
Required Qualifications
  • HS diploma or GED + 1 year of relevant experience or AS degree in a related field.
Preferred Qualifications
  • 1–2 years of experience in a manufacturing, production, or inventory control environment.
  • Experience working in a GMP or regulated industry (pharmaceutical, biotech, medical device, etc.).
  • Familiarity with electronic batch records and inventory management systems.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH

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