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Manufacturing Associate

  1. East Coast
  1. Contract
Competitive
  1. CAPEX Projects
15-09-2023
32127
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Manufacturing Associate - Boston - 6-Month Contract

Working alongside our client, a global innovator in Cell & Gene Therapy, as their newest Manufacturing Associate  you will be responsible for providing support to CDMOs, particularly related to development and GMP manufacturing of gene-edited cell therapy drug products.

Led by mission-driven and visionary scientists, our client is truly passionate about their impact on the discoveries of cell gene and therapy. Your role here will make a difference to the world and is a contract you can be proud of.


Your Responsibilities
  • Works with other manufacturing associates utilizing current good manufacturing practices (cGMPs) to aseptically manufacture clinical and commercial products using Standard Operating Procedures (SOPs).
  • Ensures right-the-first-time performance of all process steps specific to the phase or stage of operation. Escalates processing and equipment issues as needed.
  • Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities.
  • Rigorously adheres to SOPs and cGMP regulations to accurately complete paper and electronic records associated with commercial manufacturing.
  • Reviews in-process cGMP documentation for completeness and accuracy.
  • Unpacks and checks materials received against specifications, maintains records of materials used and rejects unsatisfactory items when necessary.
  • Prepares products for final shipment and maintains records of products shipped.
  • Examines, stocks, and distributes GMP and non-GMP materials to inventory and manufacturing lines.
  • Helps drive the safety-first culture
  • Applies job skills and company policies and procedures to complete a narrow range of tasks

Requirements
  • Associates or Bachlor's Degree in Science highly desired.
  • 1-2+ years of experience exemplifying Good Documentation Practices and Good Manufacturing Practices is required.
  • 1-2+ years of experience working in medical device, pharma or biotech is mandatory.
  • Must be able to read and understand quality documents.
  • Must be able to read, write and communicate fluently in English.

If this role is of interest to you, please apply now! 

The candidate must have the rights to work in the location stated in the job advert.

Please note, Quanta part of QCS Staffing does not sponsor Visa applications.

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