Senior Associate Scientist I, Biochemical Analysis

Catalent Pharma Solutions•Kansas City, MO
•Onsite

About The Position

The Senior Associate Scientist I is primarily responsible for testing samples, participating in method transfer and validation activities, drafting methods, and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. The position is based at Catalent’s Kansas City facility, a center for integrated development, manufacturing, and packaging of oral solid dosage forms, with modern laboratories and specialized capabilities supporting pharmaceutical development and commercial supply.

Requirements

  • Bachelor’s degree in Life Sciences or Physical Science with at least 2 years of relevant experience, or a master’s degree in Life Sciences or Physical Science with no experience required.
  • Knowledge of scientific principles in disciplines such as Biology, Chemistry, or Biochemistry.
  • Experience working in a laboratory environment with analytical techniques.
  • Experience or exposure to cGMP regulations and compliance requirements.
  • Strong written and verbal communication skills.
  • Strong attention to detail and documentation accuracy.
  • Ability to multitask and manage multiple priorities.
  • Ability to work independently and meet deadlines in a fast-paced environment.

Nice To Haves

  • Experience with analytical techniques such as HPLC/UPLC, electrophoresis, and spectroscopy.

Responsibilities

  • Perform sample testing for biologics under cGMP regulatory guidance.
  • Participate in method transfer and validation activities.
  • Draft methods, method forms, and analytical reports.
  • Execute laboratory testing using techniques such as HPLC/UPLC, electrophoresis, spectroscopy, and compendial assays.
  • Follow standard operating procedures with strong attention to detail.
  • Ensure accurate, legible, and compliant documentation in accordance with cGMP.
  • Perform peer review of laboratory notebooks, logbooks, and method documentation.
  • Operate laboratory equipment safely and in compliance with procedures.

Benefits

  • Competitive medical benefits and 401K.
  • 152 hours of PTO and 8 paid holidays.
  • Opportunity to work on Continuous Improvement Processes.
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