Specialist - QA

Julphar; Ras Al Khaimah; Presencial; AED 80.000 - 110.000; Jornada completa

Descripción de la vacante

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.

Formación

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

Responsabilidades

• 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.

Conocimientos

GMP

SOPs

batch records

Quality Management Systems

Educación

Bachelor's degree in Pharmacy, Science or Chemical Engineering

Descripción del empleo

Job Location

Ras Al Khaimah, United Arab Emirates

Job Reference/ID

733553222

Job Description / Role

The position is responsible for ensuring manufacturing and packaging operations meet cGMP, SOP and product requirements through shop-floor quality oversight, accurate batch documentation and effective handling of quality issues.

Key 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 corrective and preventive actions (CAPA) and change control reports (CCR) in Ampelogic.
• Prepare Annual Product Quality Reviews (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 appropriate PPE and contribute to risk reduction and continual improvement.

Experience Required

3+ years in quality operations or manufacturing.

Education Qualifications

Bachelor’s degree in Pharmacy, Science or Chemical Engineering.

Skills Required

• GMP
• SOPs
• batch records
• Quality Management Systems (QMS)

Employment / Job Type

Full Time

About the Company

A pharmaceutical manufacturer based in Ras Al Khaimah producing generic medicines, diabetes care, consumer health and nutrition products. Its facilities supply markets across the Middle East, Africa and Asia, supported by production, quality, research and commercial teams.

Company Industry

Pharmaceutical

Department / Functional Area

Quality Assurance

Closing Date

Not mentioned (apply as soon as possible)