Teams at Centrient Pharmaceuticals

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.

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.

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