At Julphar, the mission is to provide a better quality of life for the entire family through best-in-class solutions delivered with compassion and professionalism. Julphar is seeking a Finished Product & Stability Team Leader (QC) at its Ras Al Khaimah headquarters to lead quality control processes and a dedicated team within the Quality Control division, ensuring compliance with regulatory standards, managing inspections, audits, data analysis, and staff training.
About This QC Leadership Role at Julphar
Core Values: Respect, Collaboration, Innovation, Integrity, and Compassion
Function: Leading finished product and stability testing within the Quality Control division
Systems Used: SAP for test data entry, review and verification; Amplelogic for eQMS actions
Compliance Focus: GLP, GMP, cGMP requirements, and current regulatory standards
🇦🇪 Why This Role in Ras Al Khaimah Matters
Strategic Location: Julphar HQ in Ras Al Khaimah — a key pharmaceutical manufacturing hub in the UAE
Industry Impact: Contribute to a mission-driven pharmaceutical company focused on patient quality of life
Leadership Growth: Lead a team of analysts, coach and train staff, and manage cross-functional relationships
Regulatory Exposure: Handle Regulatory Authority audits and questions, building strong compliance expertise
Position Overview
This Finished Product & Stability Team Leader (QC) role at Julphar HQ involves planning and supervising the QC finished products and stability team, operating QC instruments and equipment, ensuring adherence to GLP, GMP, and safety procedures, and entering, reviewing, and verifying test data on SAP. You will prepare and update SOPs, coordinate with production plants, supervise technology transfer projects, and be responsible for the release or rejection of finished products and stability results.
Why This Role Matters: As QC Team Leader at Julphar, you directly safeguard the quality and safety of pharmaceutical products reaching patients, lead and develop a team of QC analysts within a values-driven organization, apply deep regulatory and cGMP expertise across finished product and stability testing, and take ownership of critical decisions on product release, investigations, and corrective actions.
Key Responsibilities
QC Team Planning & Supervision
- Responsible for the planning and supervision of all QC finished products and stability team, maintaining online compliance in all activities
- Operate various Quality Control (QC) instruments and equipment depending on the assigned section
- Supervise and follow up with analysts in the finished products and stability team to ensure accuracy, compliance, and timely completion of activities
Compliance & Documentation
- Ensure adherence to Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and safety procedures while maintaining a clean and hygienic laboratory environment
- Enter, review, and verify test data on the SAP system
- Prepare, review, and update Standard Operating Procedures (SOPs) related to finished product and stability testing and inspection activities
- Follow and ensure data integrity and good documentation practices are implemented in the QC labs
Production Coordination & Product Release
- Coordinate with production plants for planning analysis
- Handle and supervise Technology transfer projects
- Responsible for the release or rejection of finished products and stability in SAP according to quality evaluation results
Team Development & Quality Investigations
- Coach, guide, and train the team to ensure a high level of competency and motivation
- Analyze quality data to identify trends and areas for improvement
- Train QC personnel on applicable procedures, specifications, and testing methods, and qualify analysts to perform various QC analysis
- Perform investigations for lab incidents, OOS, OOL results, and deviations, taking appropriate corrective and preventive actions
- Follow up and close all eQMS actions (CAPA, OOS, Deviations, CC) using the Amplelogic system
Audit Support & Regulatory Adherence
- Involve and support external and internal audits, closing audit observations on time
- Adhere to cGMP principles across premises, personnel, equipment, documentation, QMS, and audits
- Check and ensure proper usage of all QC premises and equipment
- Complete other assigned work from the Head of Department or designee
Qualifications & Requirements
Educational Requirements
- Bachelor’s degree in Pharmacy
Experience Requirements
- Minimum 7 years of experience in QC/QA department
- Proven experience in quality control, with demonstrated leadership skills
- Experienced in managing complex and sensitive operational challenges
- Strong knowledge of regulatory requirements and quality standards relevant to the pharmaceutical industry
About Julphar’s Quality Control Environment
Julphar operates with a mission to deliver a better quality of life for the entire family through best-in-class pharmaceutical solutions, guided by core values of Respect, Collaboration, Innovation, Integrity, and Compassion. As QC Team Leader at Julphar HQ in Ras Al Khaimah, you play a central role in ensuring finished products and stability testing meet rigorous cGMP and regulatory standards, while leading a team through world-class research and quality assurance practices.
Diversity & Inclusion: Julphar values people from different backgrounds and is committed to diversity, inclusion, and equal opportunities across its workforce.
Who Should Apply?
- Pharmacy Graduates: With 7+ years of QC/QA experience in pharmaceutical manufacturing
- QC Team Leads/Supervisors: Experienced in finished product and stability testing
- Regulatory Compliance Professionals: With hands-on experience handling Regulatory Authority audits
- Quality Systems Specialists: Familiar with SAP, eQMS, CAPA, OOS, and deviation management
- Team Leaders: Skilled in coaching, training, and managing pharmaceutical QC analysts
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