GMP/GLP QC Documentation Specialist

Acino International AG; Dubai; On-site; AED 70,000 - 90,000; Full time

Job summary

A leading pharmaceutical company in Dubai is seeking a Quality Control – Document Administrator. Responsibilities include managing QC documentation and ensuring compliance with GLP and GMP principles. Ideal candidates have a Bachelor’s in science or pharmacy and 1-3 years of relevant experience. Strong organizational skills and attention to detail are essential. The position offers an exciting opportunity to contribute to a dynamic organization.

Qualifications

• 1-3 years of experience in pharmaceutical QC role (GLP/GMP environment preferred).
• Knowledge of data integrity (ALCOA+), GLP, and regulatory requirements.
• Familiarity with digital quality/document management systems is an advantage.

Responsibilities

• Manage QC documents in compliance with ALCOA++ principles.
• Ensure timely drafting, revision, approval, and archival of documents.
• Monitor adherence to GLP practices within the QC laboratory.

Skills

Organizational skills

Attention to detail

Ability to manage multiple priorities

Education

Bachelor’s degree in science or pharmacy

Tools

SAP

LIMS

Job description

A leading pharmaceutical company in Dubai is seeking a Quality Control – Document Administrator. Responsibilities include managing QC documentation and ensuring compliance with GLP and GMP principles. Ideal candidates have a Bachelor’s in science or pharmacy and 1-3 years of relevant experience. Strong organizational skills and attention to detail are essential. The position offers an exciting opportunity to contribute to a dynamic organization.