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Analyst II, QC Cell and Molecular Biology

Newark, CA 94560

Posted: 06/06/2024 Employment Type: Contract Job Category: Scientific Job Number: 604364 Is job remote?: No Country: United States

Job Description


Job Responsibilities
  • Support method optimization, validation and method transfer, and critical reagent qualification by executing as instructed.
  • Perform QC analytical testing to support the release and stability of final products to support the release of products for commercial use, with consideration of compliance, quality, and consistency.
  • Review test methods data and supporting documentation.
  • Maintains GMP laboratories by monitoring lab equipment, pipettes, etc. and availability of lab supply.
  • Support minor equipment troubleshooting, laboratory maintenance, and cleaning activities.
  • Manage GMP and non-GMP samples, order and receive lab reagents and materials, and manage the inventories.
  • Accurately follow relevant SOPs, performs all activities in accordance with cGMP requirements reports abnormalities.
  • Document test results to ensure completeness and accuracy per cGMP. Keeps accurate documentation and tracks record.
  • Support troubleshooting with minor assay performance issues.
  • Support discrepancy management investigations and implementation of corrective and preventative actions as instructed.
  • Contribute toward the development and revision of SOPs and Test Methods.
  • Support Change Control by gathering and providing information necessary to support simple changes to existing methods.
  • Perform non-routine laboratory tasks.
  • Other duties as assigned.
Skills:
  • Demonstrated knowledge of laboratory techniques such as Flow cytometry, ELISA, Cell culture and Cell-based assay, PCR etc.
  • Must have previous working experience in aseptic technique.
  • Experience in maintenance of GMP laboratory, laboratory equipment, and the status of pipettes and supplies. Able to perform QC laboratory maintenance related duties as assigned
  • Able to follow instructions and SOPs precisely and able to make/keep accurate and contemporaneous documentation.
  • Experience of supporting analytical method validation and transfer and reagent qualification.
  • Experience of supporting troubleshooting and optimization of the method to improve the performance.
  • Experience of supporting Invalid, OOE, and OOS investigation and CAPA initiation.
  • Able to solve minor problems and troubleshoot, as necessary.
  • Good organizational and planning skills, and an ability to work efficiently.
  • Able to learn new skills rapidly and achieve proficiency.
  • Able to seek and accept input from more senior team members for the performance of assignments as needed.
  • Able to multi-task and adapt to changing business requirements in a dynamic corporate environment.
  • Good communication skills. Able to maintain good interaction with peers and leadership within Quality Control
  • Physically able to lift LN2 freezer rack or move up to 20L buffer if needed as laboratory activities.
Education:    
  • B.S. degree in a scientific discipline with 3+ years of experiences in a cGMP compliant environment or equivalent combination of education and experience.
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