Position Overview
Responsibilities:
Review and release raw materials, intermediates, and finished productsAssess batch records, deviations, and ensure compliance with cGMP standardsProvide quality guidance on manufacturing issues, change control, and deviationsSupport operations through on-plant presence and regular Gemba walksLead investigations, support audits, and drive effective CAPAsMonitor quality trends and contribute to continuous improvement initiativesMaintain and approve key quality documentation ( SOPs, protocols, agreements)What You Need to Succeed (minimum qualifications):
Degree level (or equivalent) with relevant experience (5 years +) working in a pharmaceutical company in a quality related function.What will give you a competitive edge (preferred qualifications):
Experience in Pharmaceutical or other regulated industry ( food, healthcare)Able to demonstrate...