What the quality assurance supervisor job in Amman involves
The supervisor oversees how the Quality Management System (QMS) works in daily practice under GMP and the regulatory rules that apply, and manages and develops the people in the QA team. The post also works with other departments to keep products compliant and uses the ERP functions that connect QA with the rest of the plant.
Responsibilities
- Supervises the QMS and keeps operations in line with GMP and regulatory requirements
- Reviews, updates and approves SOPs and quality documentation, with attention to data integrity
- Oversees deviation investigations, root cause analysis and CAPA, and follows up on change control
- Reviews batch manufacturing and packaging records and handles their release
- Tracks quality performance and drives continuous improvement
- Leads and develops the QA team, working with other departments on product quality and compliance
Requirements
- Strong knowledge of GMP guidelines and pharmaceutical regulatory requirements
- Practical experience in QMS, CAPA, deviation management, change control and quality documentation
- Proven experience dealing with regulatory authorities and handling regulatory inspections
- Practical skill in batch record review and release
- Good understanding of ERP systems as used in pharmaceutical QA
- Excellent analytical, problem-solving and organizational skills, with strong communication, leadership and decision-making
- Very good written and spoken English
Preferred qualifications
- Previous supervisory or managerial experience, which the company describes as highly preferred
How to apply
CVs are sent to the email address below with “QA Supervisor” in the email subject line.
Send your CV to: [email protected]
Apply for this jobApplying is free and goes directly to the employer.
