Analytical Development Scientist II - Impactful CDMO Role

Kindeva Drug Delivery; Missouri; On-site; USD 85,000 - 125,000; Full time

Job summary

Kindeva Drug Delivery is hiring an Analytical Development Scientist II to support method transfer, verification, and validation for biologics and small molecules in a CDMO setting. You will collaborate across Manufacturing, Quality, Validation, and Technical Operations to ensure compliant analytical activities and robust data integrity.

The role requires a strong background in analytical chemistry, hands-on experience with HPLC/LC-MS, and disciplined documentation.

Qualifications

• Over 5 years of industry experience in GMP-regulated pharma/CDMO.
• Experience with biologics and small molecule products.
• Hands-on analytical method transfer, validation, verification, and testing.
• Proficiency with chromatography data systems and lab software.
• Strong data analysis, statistics, and technical documentation.

Responsibilities

• Execute analytical method transfer, verification, validation, and troubleshooting for biologic and small molecule products.
• Perform routine and non-routine analytical testing of materials, in-process samples, and finished products.
• Support investigations, regulatory submissions, cleaning validation, and manufacturing support.
• Maintain and qualify analytical instrumentation and laboratory systems.
• Identify improvements to methods, processes, efficiency, and data integrity.
• Collaborate with QC, Manufacturing, QA, Validation, and Technical Operations; provide training.
• Author methods, SOPs, protocols, and reports with cGMP and GDP compliance.
• Support off-shift, weekend, or manufacturing-related activities as needed.

Skills

Analytical method development

Data analysis

Cross-functional collaboration

Education

Bachelor's degree in Chemistry

Master's degree in Chemistry/Biochemistry

PhD in related field

Tools

Empower

Chromeleon

HPLC

UPLC

LC-MS

Job description

Kindeva Drug Delivery is hiring an Analytical Development Scientist II to support method transfer, verification, and validation for biologics and small molecules in a CDMO setting. You will collaborate across Manufacturing, Quality, Validation, and Technical Operations to ensure compliant analytical activities and robust data integrity.

The role requires a strong background in analytical chemistry, hands-on experience with HPLC/LC-MS, and disciplined documentation.