Analytical Chemist – GMP Pharma (Onsite in Irvine, HPLC)

Actalent; California; Vor Ort; USD 71.000 - 83.000; Vollzeit

Benefits dieser Stelle

Dental coverage

Vision coverage

Sign-on bonus

Paid time off

Holiday pay

Zusammenfassung

Actalent in Irvine, CA is seeking an Analytical Chemist to perform analytical testing in a GMP-regulated environment, focusing on method development and validation, data analysis, and cross-functional collaboration to support product development and commercial activities.

The role involves operating HPLC systems, method validation, documentation, and collaboration with Quality and Manufacturing to ensure high-quality data and compliant processes.

Qualifikationen

• Bachelor's degree in Chemistry or related field required.
• 2–5+ years of analytical chemistry in GMP environment preferred.
• Experience operating HPLC systems for routine and specialized testing.
• Experience with analytical method validation and method transfer.
• Pharmaceutical industry experience in product development or manufacturing welcome.
• GMP documentation, data integrity, and record-keeping proficiency.
• Ability to interpret analytical data and communicate results in reports.
• Strong attention to detail and compliance with quality systems.

Aufgaben

• Perform analytical testing using HPLC and other instruments in a GMP environment.
• Execute method validation, transfer, and troubleshooting to ensure robust methods.
• Analyze and interpret laboratory data with accuracy and integrity.
• Author and review protocols, test methods, and validation reports.
• Collaborate with Quality, Manufacturing, and cross-functional teams.

Kenntnisse

BSc in Chemistry

Analytical experience

HPLC operation

GMP knowledge

Data integrity

Technical reporting

Attention to detail

Ausbildung

Bachelor's degree in Chemistry

Tools

HPLC systems

Jobbeschreibung

Actalent in Irvine, CA is seeking an Analytical Chemist to perform analytical testing in a GMP-regulated environment, focusing on method development and validation, data analysis, and cross-functional collaboration to support product development and commercial activities.

The role involves operating HPLC systems, method validation, documentation, and collaboration with Quality and Manufacturing to ensure high-quality data and compliant processes.