Associate Scientist II

Catalent Pharma Solutions•Kansas City, MO
•Onsite

About The Position

Catalent’s Kansas City facility houses its Oral & Specialty Drug Delivery, Biologics Analytical Services, and Clinical Supply Services businesses. The Associate Scientist II will join the Molecular & Cellular Biology team and perform sample testing and data reporting under cGMP regulatory guidance in support of Large Molecules/Biologics product development, release, and stability studies. The role contributes to biologics therapeutics through high-quality, compliant laboratory operations and uses a range of molecular and cellular biology techniques. This is a 100% onsite position in Kansas City, Missouri, with a Monday–Friday, 8:00 a.m.–5:00 p.m. schedule. The role requires following standard operating procedures, maintaining accurate and thorough cGMP documentation, operating laboratory equipment safely, and supporting the preparation of simple methods, method forms, and result reports. The Associate Scientist II will train on one or two methods or techniques and perform ad hoc sample testing as required. A bachelor’s degree in a life sciences or physical science field is required; no prior work experience is required. GMP experience is preferred.

Requirements

  • Bachelor’s degree in a life sciences or physical science field.
  • No work experience required.
  • Applied knowledge of the principles and concepts of a discipline such as Biology, Chemistry, or Biochemistry.
  • Excellent written and verbal communication skills with internal customers, colleagues, and supervisors.
  • Strong organizational skills and the 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 provided in written, oral, diagram, or schedule form.
  • Ability to stand, walk, and sit frequently; lift up to 40 pounds; push and pull up to 35 pounds; and kneel and reach occasionally.

Nice To Haves

  • Good Manufacturing Practice (GMP) experience.

Responsibilities

  • Execute laboratory testing in support of Large Molecules/Biologics therapeutics using mammalian cell culture, sterile technique, and in vitro cell-based assays such as reporter gene bioassays and CellTiter-Glo proliferation bioassays.
  • Perform quantitative and potency ELISA assays using fluorescence, luminescence, colorimetric, or MSD methods.
  • Conduct molecular biology techniques, including quantitative polymerase chain reaction (qPCR) and polymerase chain reaction (PCR).
  • Perform kinetic binding assessments using techniques such as biolayer interferometry (BLI) or surface plasmon resonance (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 sample testing activities under cGMP as required.
  • Apply basic scientific and laboratory concepts and theories to assigned testing.
  • Follow cGMP requirements and maintain legible, accurate, and thorough documentation for 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 concerning quality, safety, and ethical practices.
  • Perform other duties as assigned.

Benefits

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