Senior Associate Scientist I, Biochemical Analysis
About The Position
Catalent’s Kansas City facility is a leading center for integrated development, manufacturing, and packaging services for oral solid dosage forms. The site combines advanced technologies with a collaborative environment to support pharmaceutical development from early-stage formulation through commercial supply. With a strong focus on quality and innovation, the campus offers modern laboratories, state-of-the-art manufacturing suites, and specialized capabilities to meet diverse client needs. This location fosters teamwork and continuous learning, making it an excellent setting for professionals who want to contribute to delivering life-changing therapies while working in a dynamic and supportive environment. The Senior Associate Scientist I is primarily responsible for testing samples, participate in method transfer and validation activities, draft methods, and report data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.
Requirements
- Bachelor’s Degree in Life Sciences or Physical Science with 2+ years of relevant experience, OR Master’s degree in Life Sciences or Physical Science (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 (HPLC/UPLC, electrophoresis, spectroscopy, etc.) preferred
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 PTO + 8 Paid Holidays
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What This Job Offers
Job Type
Full-time
Career Level
Senior
