Associate Scientist II - Molecular & Cellular Biology

Medvacon Life Sciences LLC

  • Kansas City, MO
  • 30+ days ago

    Highlights

    In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.) § ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD) § Molecular biology (e.g., qPCR, PCR, etc.) § Kinetic binding assessment (e.g., BLI or SPR) § Flow cytometry § Other technologies/methodologies as required by management. Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.

    Numbers & Facts

    LocationKansas City, MO

    Description

    TEMP TO HIRE - DURATION - 6 MONTHS - ONSITE POSITION - SHIFT - MON-FRI 8AM - 4PM.

    I. Position Overview

    Associate Scientist II is primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.

    In support of Large Molecules/Biologics Biologics Therapeutics, will execute laboratory testing using the following techniques as required:

    § Mammalian cell culture

    § Sterile technique

    § In vitro cell based assays (e.g., reporter gene bioassay, cell titer glo proliferation bioassay, etc.) § ELISA assays, quantitative and potency (fluorescence, luminescence, colorimetric, MSD) § Molecular biology (e.g., qPCR, PCR, etc.) § Kinetic binding assessment (e.g., BLI or SPR) § Flow cytometry § Other technologies/methodologies as required by management

    II. Essential Functions

    • Reads and follows Standard Operating procedures with attention to details
    • Successfully trains on 1-2 methods and/or techniques mentioned above and performs adhoc sample testing activities under cGMP as required
    • Applies basic scientific and laboratory concepts and theories related to specific testing in the group
    • Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports.
    • Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner
    • Understands the culture, programs, and communication processes regarding quality, safety, and ethical practices
    • All other duties as assigned

    III. Position Requirements

    Education and Experience:

    • Bachelor's Degree in Life Sciences or Physical Science field. No work experience required

    Knowledge/Skills Requirements:

    • Has basic knowledge of the principles and concepts of a discipline (e.g., Biology, Chemistry, Biochemistry).
    • Excellent written and verbal communications skills with internal customers, colleagues, and supervisor
    • Well organized with ability to multitask and be flexible with daily work schedule
    • Ability to work effectively under pressure to meet deadlines
    • Ability to pay attention to detail and exhibit critical thinking

    Important Notice: Protecting Your Information

    Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com.

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