Scientist I, BioChemical Analysis

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Competitive medical benefits

401K

PTO + Holidays

Continuous Improvement

Job summary

Catalent Pharma Solutions in Kansas City invites a Scientist I, BioChemical Analysis to join a dedicated team supporting cGMP biologics work. You will perform method evaluation, transfer, and validation, and contribute to method lifecycle documentation in a fast-paced development environment.

Responsibilities include analytical testing (HPLC/UPLC, CE, spectroscopy), drafting technical documents, and coaching peers on methods and lab practices while ensuring compliant records and continuous

Qualifications

• Degree in Life Sciences or Physical Science with 6+ years experience, or
• Master's with 4+ years experience, or Doctorate in Life Sciences or Physical Science.
• Applied knowledge of analytical principles and cGMP environment.

Responsibilities

• Perform method evaluation, optimization, transfer, and validation under cGMP.
• Execute analytical testing for biologics using HPLC/UPLC, CE, spectroscopy.
• Draft and review technical documents including methods, validation protocols, and reports.
• Train peers on methods, instrumentation, and lab practices; ensure compliant records.

Skills

cGMP compliance

Method development

Transfer & validation

Technical documentation

Education

Bachelor's Degree in Life Sciences or Physical Science

Master's Degree

Doctorate Degree

Tools

HPLC/UPLC

CE

Spectroscopy

Job description

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 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.

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 [e-mail]. 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.

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