Scientist I, BioChemical Analysis

Catalent

Kansas City (MO)

On-site

USD 65,000 - 90,000

Full time

44 hours ago
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Benefits offered by this job

Competitive medical benefits and 401K
152 hours PTO + 8 Paid Holidays
Dynamic, fast-paced work environment
Continuous Improvement Processes

Job summary

Catalent's Kansas City facility is a leading center for integrated development, manufacturing, and packaging of oral solids. The Scientist I executes method evaluation, transfer, and validation under cGMP, performing analytical testing with HPLC/UPLC, electrophoresis, spectroscopy, and compendial assays.

The role requires a Bachelor's with 6+ years, or a Master's with 4+ years, or a PhD in Life or Physical Sciences, plus experience drafting methods and reports and training peers.

Qualifications

  • Bachelor's, Master's, or Doctorate with relevant experience in biologics/chemistry.
  • Experience in cGMP regulated environments and method development.
  • Drafting protocols, methods, and validation reports with attention to detail.

Responsibilities

  • Perform method evaluation, transfer, and validation under cGMP guidance.
  • Execute analytical testing for biologics using HPLC/UPLC, CE, spectroscopy.
  • Draft and review methods, validation protocols, and technical reports.
  • Train peers on methods, instrumentation, and laboratory practices.
  • Maintain compliant documentation and perform peer-review of notebooks.

Skills

Applied knowledge
cGMP experience
Analytical methods

Education

Bachelor's Degree in Life Sciences or Physical Science
Master's degree in Life Sciences or Physical Science
Doctorate in Life Sciences or Physical Science

Tools

HPLC/UPLC
CE
Spectroscopy

Job description

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 Scientist I is primarily responsible for method evaluation, optimization, transfer and validation activities under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies. Also responsible for drafting technical documents such as methods, method forms, validation protocols and reports.

The role
  • Perform method evaluation, optimization, transfer, and validation activities under cGMP guidance
  • Execute analytical testing for biologics using techniques such as HPLC/UPLC, electrophoresis, spectroscopy, and compendial assays
  • Draft and review technical documents including methods, validation protocols, and reports
  • Perform ad hoc sample testing and support method lifecycle activities
  • Follow standard operating procedures with strong attention to detail
  • Ensure accurate, legible, and compliant documentation in accordance with cGMP requirements
  • Perform peer review of laboratory notebooks, logbooks, and technical documentation
  • Train and coach peers on methods, instrumentation, and laboratory practices
The candidate
  • Bachelor's Degree in Life Sciences or Physical Science with 6+ years of relevant experience, OR
  • Master's degree with 4+ years of relevant experience, OR
  • Doctorate degree in Life Sciences or Physical Science
  • Applied knowledge of scientific principles in Biology, Chemistry, or Biochemistry
  • Experience with analytical techniques (HPLC/UPLC, CE, spectroscopy, etc.)
  • Experience working in a cGMP-regulated environment
  • Experience with method development, transfer, validation, or optimization
  • Experience drafting/reviewing technical documents (methods, protocols, reports)
Why you should join Catalent
  • Competitive medical benefits and 401K
  • 152 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 DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.

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