Analytical Development Scientist II: Transfer & Validation

Kindeva; Bridgeton (MO); On-site; USD 95,000 - 125,000; Full time

Job summary

Kindeva is seeking an Analytical Development Scientist II in Bridgeton, MO. You will develop and transfer analytical methods for biologics and small molecules, perform routine and validation testing, and investigate methods and processes to ensure quality and compliance.

You will work with QC, Manufacturing, Validation, and Technical Operations to deliver high‑quality data and support regulatory submissions.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry or related field with 5+ years of industry experience; higher degrees reduce needed experience.
• Experience supporting QC or Analytical Development in GMP-regulated environments, including biologics and small molecules.
• Hands-on analytical method transfer, validation, and testing using HPLC/UPLC, LC-MS, GC-MS, FTIR, SDS-PAGE, ELISA, and related assays.
• Strong documentation, data integrity, and familiarity with cGMP regulations and GDPs.

Responsibilities

• Execute method transfer, verification, validation, and troubleshooting for biologic and small‑molecule products.
• Perform routine and non‑routine analytical testing of materials and finished products.
• Support investigations, specification development, regulatory submissions, and cleaning validation.
• Collaborate with QC, Manufacturing, Validation, and Technical Operations to ensure compliant analytical activity.

Skills

HPLC/UPLC

LC-MS/GC-MS

SDS-PAGE/Western blot

ELISA and protein assays

Karl Fischer titration

pH analysis

Empower/Chromeleon software

cGMP knowledge

Data interpretation & reporting

Cross-functional collaboration

Education

Bachelor's degree in Chemistry/Biochemistry

Master's degree in related field

Ph.D. in related field

Tools

Empower

Chromeleon

Job description

Kindeva is seeking an Analytical Development Scientist II in Bridgeton, MO. You will develop and transfer analytical methods for biologics and small molecules, perform routine and validation testing, and investigate methods and processes to ensure quality and compliance.

You will work with QC, Manufacturing, Validation, and Technical Operations to deliver high‑quality data and support regulatory submissions.