Biomanufacturing Associate

Pay Rate Low
: 20 |
Pay Rate High
: 22

Join a global, science-driven biopharmaceutical organization known for its commitment to quality, patient safety, and operational excellence. This position supports a 24/7 manufacturing operation using a rotating schedule on day shift.

Location
:
West Greenwich, RI

Schedule
: 6:30am-7pm, days rotate

Pay
: $20/hr - $22/hr

Contract Role**

• Support downstream biopharmaceutical manufacturing operations within a GMP-regulated production environment, including process activities such as chromatography, viral inactivation/neutralization, depth filtration, ultrafiltration/diafiltration, and final product processing.
• Perform in-process testing and quality checks, including UV, pH, conductivity, endotoxin, and TOC analysis, while maintaining compliance with established procedures and quality standards.
• Execute manufacturing activities in accordance with Good Manufacturing Practices (GMPs), Standard Operating Procedures (SOPs), and applicable regulatory requirements.
• Review and complete batch documentation, electronic records, and manufacturing paperwork to ensure accuracy, compliance, and right-first-time execution.
• Identify and elevate process discrepancies, equipment issues, or documentation concerns to appropriate team members to support quality and safety objectives.
• Prepare, stage, and handle manufacturing components and materials required for production activities.
• Operate and support manufacturing equipment, including performing equipment setup, material loading, and routine sanitation activities.
• Utilize inventory management systems and electronic documentation platforms to track materials, production activities, and batch records.
• Monitor manufacturing performance metrics and participate in daily production meetings to support operational goals and continuous improvement initiatives.
• Safely move materials and equipment using manual and powered pallet jacks as needed.
• Collaborate with cross-functional teams including manufacturing, quality, and support groups to maintain efficient production operations.

• BS degree in a scientific field OR
• 0-2 years of related manufacturing experience in a GMP environment

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