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Randstad in partnership with one of the largest pharmaceutical companies in the world is seeking a Research Associate for mRNA Manufacturing of Personalized Cancer Vaccines based at their GMP Manufacturing site in Norwood, MA.
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Skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, GMP (Good Manufacturing Practice) - Operate general manufacturing equipment in strict accordance with SOPs to complete tasks as noted above as well as large scale bioreactor operations, critical small or large volume sterile fills, and aseptic manipulation of cell cultures.
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Technical understanding of Drug Product (DP) manufacturing operations, such as buffer batching, DP formulation, DP Filling, Inspection. Change control ownership, ensuring records are comprehensive and compliant per GMP regulatory procedures.
TemporaryExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Experience with manual visual inspection and/or laboratory in a GMP regulated environment. Able to perform initial review of manufacturing/laboratory procedures/batch records. 4 years of experience in a biotech/pharma manufacturing/laboratory or manufacturing support (i.e. laboratories, engineering, facilities, quality.
$28 - $30 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Materials Control Associate I is accountable for GMP (Good Manufacturing Practices) materials control/warehousing operations for a Phase II/III GMP biopharma manufacturing facility.
$20 - $25 an hourExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Job Summary The operations associate position is a general labor role that executes production and manufacturing activities. Ensure that work procedures are being followed in a consistent manner (Safety, Quality, GMP, MAV and HACCP.
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Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific merits of Chemistry, Manufacturing and Control (CMC) and nonclinical study data package.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Materials Control Associate III is accountable for GMP (Good Manufacturing Practices) materials control/warehousing operations for a Phase II/III GMP biopharma manufacturing facility.
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The Manufacturing Associate I/II - Downstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. Position Responsibilities The Manufacturing Associate I/II - Downstream must follow the instructions depicted in SRs, EPRs, SOPs and forms.
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The Associate Director provides technical leadership and support across multiple CMC biologics areas to drive downstream process development, technology transfer, and manufacturing of biological drug candidates with a focus on therapeutic proteins' purification process development.
$131,500 - $195,500 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Comply with Food Manufacturing Good Manufacturing Practices (GMP) policy to ensure quality and safety standards are met. As a janitorial associate, you will play a crucial role in maintaining a clean and organized work environment.
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Exposure to cGMP's, established manufacturing practices and procedures, and compliance with GMP, QS, and ISO regulations and guidelines. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications.
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Understand and adhere to Lock-Out/Tag-Out (LOTO) Procedures, Confined Space Procedures and all other Plant Safety/Good Manufacturing Practices (GMP) requirements related to supporting machinery uptime.
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The chosen applicant will perform daily operations related to storing product and loading trucks in an efficient manner while following company rules while also being responsible for following food and safety requirements pertaining to BRC AIB GMP and any other legal or legislative rules/regulations.
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Job Title: Sample Management Associate / LIMS / Pharma Manufacturing. Responsible for supporting the sample management process for QC (pick up from manufacturing, maintaining chain of custody in LIMS, aliquoting/delivering samples to appropriate lab, etc.
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