Onsite Analytical Scientist I: Method Dev & QA

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

Tuition reimbursement

PTO & holidays

Job summary

Catalent's Kansas City facility seeks an Analytics Senior Associate Scientist I to execute laboratory work plans, perform analyses with HPLC, GC, and related techniques, and contribute to method development. You will maintain rigorous documentation and support regulatory compliance in a fast-paced, collaborative setting.

The role emphasizes training teammates, driving efficiency projects, and ensuring quality across in-process, release, and stability samples.

Qualifications

• Bachelor's degree in a related life science or physical science is required.
• Strong written and verbal communication skills with internal and external customers.
• Well organized with the ability to multitask and manage time efficiently.
• Basic understanding of instrument operations and troubleshooting across multiple techniques.

Responsibilities

• Execute laboratory work plans and schedules.
• Perform analyses using techniques such as HPLC, GC, Karl Fischer, and tablet testing.
• Develop, validate, and transfer analytical methods.
• Maintain accurate laboratory documentation per SOPs and regulations.
• Draft methods or certificates of analysis and participate in technical reviews for accuracy.

Skills

Attention to detail

Written communication

Verbal communication

Organization

Multitasking

Regulatory awareness

Education

Bachelor's degree in life or physical science

Master's degree in life or physical science (preferred)

Tools

HPLC

GC

Karl Fischer

Disintegration

Friability

Hardness testing

Appearance testing

Job description

Catalent's Kansas City facility seeks an Analytics Senior Associate Scientist I to execute laboratory work plans, perform analyses with HPLC, GC, and related techniques, and contribute to method development. You will maintain rigorous documentation and support regulatory compliance in a fast-paced, collaborative setting.

The role emphasizes training teammates, driving efficiency projects, and ensuring quality across in-process, release, and stability samples.