Associate Scientist II

Catalent•Kansas City, MO
•Onsite

About The Position

The Associate Scientist II joins Catalent’s Molecular & Cellular Biology team at its Kansas City facility. The role tests samples and reports data under cGMP regulatory guidance in support of Large Molecules/Biologics product development, release, and stability studies. It involves laboratory testing with molecular and cellular biology techniques and contributes to high-quality, compliant laboratory operations. The position is 100% onsite in Kansas City, Missouri, with a Monday–Friday schedule from 8 a.m. to 5 p.m.

Requirements

  • Bachelor’s degree in a Life Sciences or Physical Science field.
  • Applied knowledge of principles and concepts in a discipline such as Biology, Chemistry, or Biochemistry.
  • Excellent written and verbal communication skills with internal customers, colleagues, and supervisors.
  • Strong organizational skills and ability to multitask and work independently on multiple projects.
  • Flexibility with the daily work schedule.
  • Ability to work effectively under pressure to meet deadlines.
  • Attention to detail and strong critical-thinking skills.
  • Ability to interpret instructions presented in written, oral, diagram, or schedule form.

Nice To Haves

  • Good Manufacturing Practice (GMP) experience.

Responsibilities

  • Execute laboratory testing for Large Molecules/Biologics therapeutics using mammalian cell culture, sterile technique, and in vitro cell-based assays, including reporter gene and cell titer glo proliferation bioassays.
  • Perform quantitative and potency ELISA assays using fluorescence, luminescence, colorimetric, or MSD methods.
  • Conduct molecular biology techniques, including qPCR and PCR.
  • Perform kinetic binding assessments using techniques such as BLI or SPR.
  • Use flow cytometry and other technologies as required by management.
  • Read and follow Standard Operating Procedures with attention to detail.
  • Train on one or two methods or techniques and perform ad hoc cGMP sample testing as required.
  • Apply basic scientific and laboratory concepts and theories to testing performed by the group.
  • Follow cGMP requirements for legible, accurate, and thorough documentation to meet regulatory compliance.
  • Support drafting simple methods, method forms, and result reports.
  • Operate laboratory equipment safely and in compliance with policies and procedures.
  • Follow Catalent’s culture, programs, and communication processes relating to quality, safety, and ethical practices.
  • Perform other duties as assigned.

Benefits

  • Competitive paid time off and eight paid holidays.
  • Medical, dental, and vision benefits effective on the first day of employment.
  • Tuition reimbursement.
  • Defined career path and annual performance review and feedback process.
  • Potential for career growth on an expanding team.
  • Diverse, inclusive culture.
  • Community engagement and green initiatives.
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