Pharma QA Specialist — GMP & Compliance

Julphar

Ras Al Khaimah

On-site

AED 80,000 - 110,000

Full time

12 days ago

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Job summary

Julphar in Ras Al Khaimah, United Arab Emirates, seeks a Quality Assurance professional to oversee manufacturing and packaging quality, ensuring cGMP adherence and accurate documentation. The role focuses on line clearances, CAPA management and audit readiness.

The ideal candidate has a 3+ year background in quality operations or manufacturing, plus a Bachelor’s degree in a relevant field. Join a leading pharmaceutical manufacturer with a commitment to quality and compliance.

Qualifications

  • GMP knowledge and application
  • SOPs adherence and documentation
  • Maintaining batch records accurately
  • Quality Management Systems (QMS) knowledge

Responsibilities

  • Perform line clearance and release activities, and timely in-process checks during manufacturing and packaging.
  • Verify correct materials/components, gowning, cleanliness, environmental conditions and calibration of in-process equipment.
  • Document and verify results; maintain traceable, accurate batch records, logbooks and labels. Review SOPs, batch manufacturing records (BMRs) and batch packaging records (BPRs).
  • Investigate deviations and market complaints. Manage CAPA and CCR in Ampelogic.
  • Prepare APQR; support audits and audit readiness, site gap assessments, GEMBA walks, sampling adherence follow-up and facility/process quality risk assessments.
  • Follow environmental, health and safety requirements, use PPE and contribute to risk reduction and continual improvement.

Skills

GMP
SOPs
batch records
Quality Management Systems

Education

Bachelor's degree in Pharmacy, Science or Chemical Engineering

Job description

Julphar in Ras Al Khaimah, United Arab Emirates, seeks a Quality Assurance professional to oversee manufacturing and packaging quality, ensuring cGMP adherence and accurate documentation. The role focuses on line clearances, CAPA management and audit readiness.

The ideal candidate has a 3+ year background in quality operations or manufacturing, plus a Bachelor’s degree in a relevant field. Join a leading pharmaceutical manufacturer with a commitment to quality and compliance.

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