Julphar
Senior Specialist – Quality Control
- Permanent
- Ras Al Khaimah, United Arab Emirates
- Experience 2 - 5 yrs
Job expiry date: 20/05/2026
Job overview
Date posted
05/04/2026
Location
Ras Al Khaimah, United Arab Emirates
Salary
AED 15,000 - 20,000 per month
Compensation
Salary only
Experience
2 - 5 yrs
Seniority
Senior & Lead
Qualification
Bachelors degree
Expiration date
20/05/2026
Job description
The Senior Specialist – QC at Julphar HQ is responsible for executing and maintaining high-quality chemical and physical testing of raw materials, finished products, and stability samples. The role ensures adherence to cGMP and GLP standards, maintains QC equipment, manages data in SAP, supports audits, and mentors junior staff while maintaining regulatory compliance and data integrity.
Required skills
Quality Control (QC) testing of RM, FP, and Stability samples
Chemical and physical analysis
Operation of QC lab equipment (HPLC, GC, etc.)
Good Laboratory Practices (GLP) and cGMP compliance
Process validation, method validation, and method transfer
Data entry and management in SAP
Troubleshooting laboratory incidents and deviations
Documentation practices and data integrity
Training and mentoring QC staff
Internal and external audit support
Quality Management System (QMS) handling: Deviations, OOS, CAPAs, AMS, Change Controls
Cross-functional collaboration
Problem-solving and analytical skills
Attention to detail and process compliance
Key responsibilities
- Carry out chemical and physical analysis of RM, FP, and stability samples
- Operate and maintain various QC equipment according to GMP/GLP standards
- Prepare and validate HPLC & GC analytical methods as per approved protocols
- Review and approve QC data and audit trails for analytical instruments
- Enter, verify, and lock QC results in SAP
- Investigate lab incidents, OOS/OOT results, deviations and implement corrective actions
- Support internal and external audits and close audit observations on time
- Train new QC personnel on procedures, specifications, and testing methods
- Review and approve protocols and reports (method validation, method transfer, process validation, stability studies)
- Manage QMS actions including Deviations, CAPAs, AMS, and Change Controls via Amplelogic
- Ensure proper documentation, data integrity, and compliance with lab safety and hygiene standards
- Assist supervisors in daily lab operations and troubleshooting
- Perform additional tasks as assigned by Head of Department
Experience & skills
- Bachelor’s degree in Pharmacy, Chemistry, or related Science field
- Minimum 2 years of relevant QC experience in pharmaceuticals
- Proficient with lab equipment, computer applications, and SAP
- Strong adherence to cGMP and GLP principles
- Excellent communication, interpersonal, and problem-solving skills
- High attention to detail, process compliance, and ownership
- Ability to work in a cross-functional environment
- Organized, disciplined, self-motivated, and adaptable to changing situations