To Apply for this Job Click Here The Chemist II is responsible for performing analytical testing of raw materials, in-process samples, finished products, and stability samples to ensure compliance with quality standards and regulatory requirements. This position supports laboratory operations in a GMP-regulated environment and contributes to data integrity, continuous improvement initiatives, and overall laboratory excellence.

Responsibilities:

Perform analytical testing using established methods, including HPLC, GC, TOC, and wet chemistry techniques. Independently conduct complex analytical testing with minimal supervision. Support method transfers, method verifications, method validations, and stability studies. Review and interpret analytical data to ensure accuracy and adherence to specifications. Troubleshoot analytical methods and laboratory instrumentation. Maintain accurate and compliant laboratory documentation. Review laboratory records and analytical results for completeness and accuracy. Assist with SOP revisions, method updates, and continuous improvement projects. Collaborate with Quality, Manufacturing, and Research & Development teams to support product quality and operational objectives. Support implementation of new laboratory technologies and process improvements. Ensure compliance with cGMP, GDP, and regulatory requirements. Follow data integrity principles and maintain accurate documentation practices. Support audit readiness activities and regulatory inspections. Adhere to laboratory safety policies and procedures. Train and mentor junior laboratory personnel on testing procedures and instrumentation.

Requirements:

Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline. 2-5 years of Quality Control or analytical laboratory experience in a GMP-regulated environment. Experience with analytical instrumentation such as HPLC, GC, UV/Vis, FTIR, dissolution systems, and TOC analyzers. Experience with chromatography data systems, preferably Empower 3. Strong understanding of cGMP requirements and laboratory compliance standards. Experience supporting investigations involving OOS, OOT, and deviations. 1467719_1786113731 To Apply for this Job Click Here