Biochemical Analysis Scientist I - Method Validation

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

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