GMP QC Analyst — Drug Product Lab & Stability

WuXi AppTec; Town of Middletown (NY); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical company in Middletown, DE seeks a QC Analyst to conduct analytical testing and support drug product manufacturing. Responsibilities include performing tests like HPLC and GC, ensuring compliance with GMP and quality standards, and maintaining accurate records. The ideal candidate will have an associate or bachelor’s degree in Chemistry or related fields and 1–3 years of relevant laboratory experience. This full-time position offers an opportunity to be part of a dedicated team in a dynamic environment.

Qualifications

• 1–3 years of QC analytical laboratory experience in a GMP-regulated environment.
• Familiarity with GMP regulations, ICH guidelines, and data integrity principles.
• Working knowledge of analytical techniques and instrumentation.

Responsibilities

• Perform QC analytical testing for drug products and raw materials.
• Maintain complete, accurate, and inspection-ready laboratory records.
• Notify the QC Analytical Lead of any out-of-specification results.

Skills

Analytical techniques

Laboratory equipment operation

Data integrity principles

GMP regulations knowledge

Education

Associate or bachelor's degree in Chemistry, Biochemistry, or related

Tools

HPLC

GC

UV-Vis

TOC

LIMS

Empower

Job description

A leading pharmaceutical company in Middletown, DE seeks a QC Analyst to conduct analytical testing and support drug product manufacturing. Responsibilities include performing tests like HPLC and GC, ensuring compliance with GMP and quality standards, and maintaining accurate records. The ideal candidate will have an associate or bachelor’s degree in Chemistry or related fields and 1–3 years of relevant laboratory experience. This full-time position offers an opportunity to be part of a dedicated team in a dynamic environment.