Analytical Process Development Associate

Amgen Inc. (IR); Thousand Oaks, Northern (CA, KY); Hybrid; USD 75,000 - 101,000; Full time

Benefits offered by this job

Stock-based incentives

Retirement plan

Health coverage

Flexible work model

Job summary

Amgen in Thousand Oaks, CA, is seeking a Process Development Associate to join the iPAS team within the Pharmaceutical Attribute Sciences group. The role focuses on pivotal analytical development, method development, validation, transfer, and GMP testing for drug substances and products across small molecules, peptides, siRNA, and ADC components.

You will work closely with analysts and scientists, document results, and support scale-up and formulation activities in a dynamic, cross-functional

Qualifications

• Bachelor's degree in Analytical Chemistry, Organic Chemistry, Physical, Pharmaceutical, Life Sciences, Engineering, or relevant.
• Strong analytical experience with small molecules, synthetic peptides, siRNA, and/or antibody-drug conjugates.
• Experience with chromatography and spectroscopic instruments.

Responsibilities

• Hand-on experience in sample preparation and analysis of synthetic in-process samples, lot release samples, and drug product formulations using chromatographic and spectroscopic techniques.
• Under supervision, apply established methodologies to develop, validate, and transfer analytical methods for drug substances and products.
• Organize and document analytical data under Good Documentation Practice.
• Transfer analytical methods to contract manufacturing or testing labs.

Skills

Analytical chemistry

Chromatography

Spectroscopy

Mass spectrometry

Education

Analytical Chemistry

Organic Chemistry

Physical Chemistry

Pharmaceutical Sciences

Life Sciences

Tools

Mass spectrometry

NMR

HPLC

GC

Job description

Amgen in Thousand Oaks, CA, is seeking a Process Development Associate to join the iPAS team within the Pharmaceutical Attribute Sciences group. The role focuses on pivotal analytical development, method development, validation, transfer, and GMP testing for drug substances and products across small molecules, peptides, siRNA, and ADC components.

You will work closely with analysts and scientists, document results, and support scale-up and formulation activities in a dynamic, cross-functional