Opportunity Description
Job Title: QC ChemistJob Description
We are seeking a dedicated QC Chemist to support batch release and stability programs within a cGMP pharmaceutical manufacturing environment. The role requires strong operational QC experience, particularly in solid oral dosage manufacturing such as tablets and capsules, within a fast-paced, production-driven setting.
Responsibilities
+ Conduct batch release and stability testing using chromatography (HPLC, UPLC, GC) and spectroscopy (UV-Vis, FT-IR).
+ Perform assay, dissolution, impurity, and related substances testing.
+ Operate and troubleshoot HPLC/UPLC instruments, ensuring routine calibration and maintenance.
+ Maintain GMP documentation and ensure audit-ready recordkeeping.
+ Manage stability samples and trend data effectively.
+ Collaborate daily with QA and Manufacturing to support production timelines.
+ Conduct OOS/OOT investigations and support CAPA activities.
We are seeking a dedicated QC Chemist to support batch release and stability programs within a cGMP pharmaceutical manufacturing environment. The role requires strong operational QC experience, particularly in solid oral dosage manufacturing such as tablets and capsules, within a fast-paced, production-driven setting.
Responsibilities
+ Conduct batch release and stability testing using chromatography (HPLC, UPLC, GC) and spectroscopy (UV-Vis, FT-IR).
+ Perform assay, dissolution, impurity, and related substances testing.
+ Operate and troubleshoot HPLC/UPLC instruments, ensuring routine calibration and maintenance.
+ Maintain GMP documentation and ensure audit-ready recordkeeping.
+ Manage stability samples and trend data effectively.
+ Collaborate daily with QA and Manufacturing to support production timelines.
+ Conduct OOS/OOT investigations and support CAPA activities.