Senior Associate Scientist , Biochemical Analysis

Senior Associate Scientist I, Biochemical Analysis Position Summary

Shift: Monday – Friday 8am-5pm 100% on-site 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.

The role:

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 cGMPPerform peer review of laboratory notebooks, logbooks, and method documentation

Operate laboratory equipment safely and in compliance with procedures

The candidate:

Bachelor’s Degree in Life Sciences or Physical Science with 2+ years of relevant experience, ORMaster’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

Experience with analytical techniques (HPLC/UPLC, electrophoresis, spectroscopy, etc.) preferred

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

Why you should join Catalent:

Competitive medical benefits and 401K152 hours PTO + 8 Paid Holidays Dynamic, fast-paced work environment

Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career!  Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.

Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to Disabili This option is reserved for individuals who require…