Jobs at Centrient Pharmaceuticals

Support RA-FDF team in preparing and maintaining regulatory dossiers and variation packages, coordinate responses to authorities, update product information and SOPs, evaluate CMC data, assist pharmacovigilance, ensure regulatory compliance and database upkeep, and escalate complex issues to senior RA staff.

Oversee production department safety, health, environment (SHE) and quality compliance; implement safety systems; manage departmental budget, costs, and KPIs; lead and develop production staff; drive continuous improvement.

Perform wet and instrumental analysis of raw, in-process, finished and stability samples; execute method development/validation, HPLC calibration, stability studies, inventory and log management, record of analysis, deviation reporting and CAPA, troubleshooting instruments, and ensure cGMP/GLP/ICH/USFDA/ISO compliance and lab safety.

Ensure products meet customer specifications and regulatory standards (cGMP/GLP/ICH/USFDA/ISO). Manage vendor qualification, audits, batch release/rejection, CoA creation, BPR and QC data review, market complaint/OOS investigations, sampling, recalls, SHE compliance and safety audits, and release batches in SAP.

Manage wastewater and VOC treatment performance, compliance with SHE and quality standards, equipment/process reliability, department budget and KPIs, and drive continuous environmental improvements.