Senior Associate Quality Control - (JP9706)

3 Key Consulting

  • Thousand Oaks, California
  • 1 day ago
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    Skills

    • Analysis Skillsunmatched
    • Analytical Chemistryunmatched
    • Asepsisunmatched
    • Assaysunmatched
    • Biological Assayunmatched
    • Biologyunmatched
    • Cell Culturesunmatched
    • Cleaning Equipmentunmatched
    • Cleanroomunmatched
    • Consultingunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Data Analysisunmatched
    • Data Cleaningunmatched
    • Data Entryunmatched
    • Data Managementunmatched
    • Documentationunmatched
    • Equipment Maintenance/Repairunmatched
    • GLP (Good Laboratory Practices)unmatched
    • High Performance Liquid Chromatography (HPLC)unmatched
    • Inventory Managementunmatched
    • Laboratory Analysisunmatched
    • Laboratory Notebookunmatched
    • Materials Managementunmatched
    • Process Analysisunmatched
    • Quality Controlunmatched
    • Record Keepingunmatched
    • Safety Complianceunmatched
    • Team Playerunmatched
    • Test Dataunmatched
    • Testingunmatched
    • Time Managementunmatched
    • Trend Analysisunmatched

    Description

    Job Title:  Senior Associate Quality Control - (JP9706)
    Location: Thousand Oaks, CA.
    Employment Type:  Contract
    Business Unit: Clinical Process and Chemical Analysis             
    Duration: 18+ months (with likely extensions)
    Notes:  Onsite
    Posting Date:  2/4/2022

    3 Key Consulting is hiring a Senior Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.

    Job Description:
    This Associate, in the Bioassay group, within client’s quality control organization will work in a dynamic team environment to support testing, and projects within the group. The successful candidate will be responsible for Bioassay lab activities including analytical testing and analysis, tracking and trending of data, lab cleaning, and equipment maintenance.

    Why is the Position Open?
    Backfill, and additional workload.

    Top Must-Have Skill Sets:
    • Pipetting
    • Aseptic technique
    • Cell culture
    • Degree: Biology Degree (Bachelors), will consider new grad

    Day to Day Responsibilities:
    • Sample potency testing using qualified cell or antigen/receptor based methodology
    • Testing
      • Execute routine and non-routine testing procedures and assays
      • Perform data analysis of testing results and communicate results to appropriate sources
      • Comply with safety guidelines
      • Learn and comply with GLP, and cGMPs, which includes, but are not limited to, the maintenance of training records, laboratory notebooks, written procedures, equipment monitoring systems and laboratory logbooks.
    • Material/Data Management
      • Responsible for documenting, computing, compiling, interpreting, and entering data
      • Responsible for the inventory management of all media, and reagents
      • Ensure the timely disposal of tested samples.

    Red Flags:
    • HPLC
    • Gels

    Interview process:
    Phone screening followed by in-person interview.

    We invite qualified candidates to send your resume to 

    resumes@3keyconsulting.com

    .  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
     

    Numbers & Facts

    LocationThousand Oaks, California
    Website3keyconsulting.com/careers

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