QC Compliance Supervisor
Skills
About This Role
Job Overview
HIBA Pharma is seeking an experienced QC Compliance Supervisor to oversee compliance-related activities within the Quality Control department in a regulated pharmaceutical manufacturing environment.
Key Responsibilities
- Monitor QC operations to ensure compliance with GMP, GLP, USP, EP, BP, and company procedures
- Review laboratory documentation, raw data, SOPs, protocols, and analytical reports
- Manage deviations, OOS, OOT, investigations, CAPA, and root cause analysis activities
- Coordinate internal audits and regulatory inspection readiness activities
- Support training activities related to compliance and documentation practices
- Collaborate with QA, Validation, and cross-functional departments
- Drive continuous improvement initiatives within the QC laboratory
Requirements
- Bachelor’s Degree in Chemistry or Pharmacy
- Minimum 5 years of QC experience in pharmaceutical manufacturing
- Minimum 2 years in quality/compliance-related role
- Strong knowledge of GMP, GLP, ICH, FDA, EMA, WHO, USP, EP, and BP guidelines
- Experience with laboratory investigations, CAPA, audits, and inspection readiness
- Strong communication and leadership skills
- Good MS Office and risk assessment knowledge
- Pay: From AED12,000.00 per month
Experience
- pharmaceutical quality control compliance : 5 years (Preferred)
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