Analytical Scientist: cGMP Lab R&D & Method Validation

WuXi AppTec; San Diego (CA); On-site; USD 69,000 - 90,000; Full time

Job summary

STA Pharmaceutical US LLC, a WuXi AppTec Company, is seeking an analytical chemist to join the Analytical Chemistry Department. The role supports routine analytical testing and data verification for process development and manufacturing in cGMP laboratories.

You will perform qualitative and quantitative assays using wet chemistry and state-of-the-art instruments, conduct HPLC and GC method validation and transfers, and maintain instruments while ensuring quality compliance and accurate

Qualifications

• Master's degree in analytical chemistry or a related field is required or BS with 1–2 years of relevant experience.
• Experience in a cGMP environment is preferred.
• Ability to perform qualitative and quantitative analyses using wet chemistry techniques and modern analytical tools.
• Experience with HPLC and GC method validation/transfer is desirable.

Responsibilities

• Support routine analytical testing and data verification for process R&D and production in cGMP laboratories.
• Perform qualitative and quantitative assays following applicable analytical methods.
• Conduct HPLC and GC method validation and transfer activities and prepare related documentation.
• Maintain instruments, troubleshoot issues, and contribute to SOPs and regulatory filings.

Skills

cGMP environment

raw material testing

qualitative & quantitative assays

HPLC

GC

documentation & regulatory filings

problem solving

teamwork

Education

Masters degree in analytical chemistry or related field

BS in analytical chemistry or related field with 1-2 years experience

Tools

HPLC

GC

Regulatory documentation (SOPs/Reports)

Job description

STA Pharmaceutical US LLC, a WuXi AppTec Company, is seeking an analytical chemist to join the Analytical Chemistry Department. The role supports routine analytical testing and data verification for process development and manufacturing in cGMP laboratories.

You will perform qualitative and quantitative assays using wet chemistry and state-of-the-art instruments, conduct HPLC and GC method validation and transfers, and maintain instruments while ensuring quality compliance and accurate