Biomanufacturing Associate

Location: West Greenwich

** Biomanufacturing Associate*
* Science & Research

West Greenwich, Rhode Island, US

+ Added - 20/07/2026

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.

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* Location:

** West Greenwich, RI

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* Schedule:

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

** Pay:**  $20/hr - $22/hr

**** Contract Role***
* ** Job Duties*
* + 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 escalate 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.

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* Qualifications:

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* + 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

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.