
Nadia Haddad
Quality Assurance Analyst
Assuring quality and compliance in regulated production
Quality assurance analyst with seven years in pharmaceutical QA at manufacturers in Amman. Protects the patient through the paperwork and the process — reviewing batch records, auditing against GMP, investigating deviations, and making sure every product released is made right and fully documented. Cleared batches without quality holds and led deviation investigations that fixed root causes for good. Reviews and approves batch documentation, audits against GMP, investigates deviations and CAPAs, maintains the quality system, and supports inspections. Rigorous, methodical and uncompromising on standards. Looking for a QA-analyst role with a regulated manufacturer where doing things right genuinely matters.
Amman Pharmaceutical Manufacturer - Amman, Jordan
Quality Assurance Analyst January 2019 to Present 7 years & 6 months
Cleared batches without quality holds and led deviation investigations that fixed root causes for good.
Review and approve batch records and documentation, confirming each batch was made exactly as it should be.
Audit production and processes against GMP, checking that what happens on the floor matches what the rules require.
Investigate deviations and drive CAPAs, finding why something went wrong and making sure it cannot recur.
Maintain the quality system and support inspections, keeping the site audit-ready and compliant at all times.
Jordan Pharma Labs - Amman, Jordan
QC/QA Officer February 2017 to December 2018 1 year & 11 months
Reviewed records and supported audits and deviations, building GMP and quality-system skills over time.
Learned batch review, GMP auditing and deviation handling on the job across nearly two years.
Gained the certificate and experience that led into a full quality-assurance-analyst role of my own.
University of Jordan
BSc in Pharmaceutical Sciences (September 2012 to June 2016)
Jordan Pharmaceutical Institute
GMP & Quality Systems Certificate (August 2016 to January 2017)
Clean batch releases
Uncompromising on standards
Fixed root causes
GMP & Quality Systems Certificate
Jordan Pharmaceutical Institute (January 2017 to Present)
- Batch Record Review
- GMP Auditing
- Deviation Investigation
- CAPA Management
- Quality Systems
- Regulatory Compliance
- Documentation Control
- Root-Cause Analysis
- Inspection Readiness
- Validation Support