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In this position the QC Inspector will be partnering with the Quality Control Supervisor assisting with the responsibility for the day to day operation of your assigned Quality Control group.
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Reporting to the Director, QC Molecular Biology, the Analyst I - QC Molecular Biology will support the gene therapy program pipeline including but not limited to routine GMP testing of AAV vector analytical methods such as GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed.
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Identifies and makes recommendations to Project Manager regarding project risks including safety/loss control, subcontractor/supplier issues, site conditions and logistics, scheduling, change orders, and document conflicts.
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Participates in Company-provided training such as safety, non-discrimination, QA/QC, and harassment prevention. The position reports to the General Superintendent. Experience in using Procore and Textura a plus.
$150,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Schedules third party inspections of work in progress and ensures responses to any exceptions or punch list items noted by the consultants and inspectors. Project Location - Weston, MAPosition SummaryThe Superintendent is responsible for coordinating and supervising all phases of the field work performed by subcontractors and vendors in constructing high density residential and mixed use projects.
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This role will help establish the microbiology function at Elevatebio, including but not limited to; laboratory/clean room start-up and qualification, development of the environmental monitoring program and contamination and control strategies, and execution of routine QC microbiology assays.
Part-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Performs special tasks as assigned by QC manager Maintains retain sample area and control sample file Maintains safe work practices and good manufacturing standards. Communicates product quality issues to Production Supervisors, Production Managers, QC Manager & Supervisor and shipping and customer service staff.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Train and teach QC employees on how to run various QC testing. Support quality control testing and run the quality control department. Job Title: Quality Control Manager.
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Role : QC Chemist. Proficiency in using gas chromatography (GC) for the analysis and separation of compounds in a mixture, commonly used in drug testing for purity and quality control. Strong foundation in the pharmaceutical industry, with an understanding of regulations, standards, and processes within drug development, manufacturing, and quality control.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System. Testing may include but not limited to samples from drug substance and drug product manufacturing, stability and various protocol studies using approved test methods or test methods derived from QC technical protocols.
$53.39 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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This position is based at Genezen's new state-of-the-art facility in Lexington, MA. This role supports the evening and occasional weekend operations within the Quality Control group via execution of analytical testing, bioassay testing and Quality Systems.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Adaptable to perform in a fast-paced environment while still delivering high-quality results, this Analyst I - QC Molecular Biology will be required to have strong interpersonal skills and be able to work under minimal supervision.
$39 an hourExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Responsible for reviewing scientific and analytical data related to pharmaceutical testing, ensuring that it meets required standards and accuracy for quality control and compliance. This could involve using equipment like HPLC (High-Performance Liquid Chromatography), dissolution testers, and more, to ensure the quality and consistency of drug products.
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The person will serve as a Subject Matter Expert in the in the quality control group and will lead the training efforts, method transfers from external CDMO, Analytical R&D to QC group. Datasheet review, QC investigation, out of specification (OOS), CAPA, Change Controls, and/or Deviation report writing experiences desired.
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We are looking for a Quality Control (QC) professional to join our team as a Senior Analyst Quality Control, supporting our internal GMP cell therapy manufacturing. Ensures maintenance and control of QC test samples.
Full-timeExpandApply NowActive JobUpdated 15 days ago
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