UAE Pharma Jobs – Process Lead, QC Manager, Production Team Leader, QA Engineering Lead & Forklift Driver

Explore Julphar UAE Pharma Jobs 2025 including Process Lead – Risk Management, Manager – Quality Control, Team Leader – Production, Team Lead QA–Engineering Oversight, and Forklift Driver roles. Detailed eligibility, responsibilities, skills, and application links included.

Julphar UAE Pharma Jobs – Process Lead, QC Manager, Production Team Leader, QA Engineering Lead & Forklift Driver Roles

The pharmaceutical job market in the United Arab Emirates continues to evolve rapidly, and Julphar (Gulf Pharmaceutical Industries), one of the Middle East’s largest and most respected pharmaceutical manufacturers, is offering multiple exceptional career opportunities across Quality, Production, Engineering Oversight, and Warehouse Operations. In this comprehensive job guide, we present all 5 openings in detail—each crafted to support professionals looking for growth in pharmaceutical manufacturing, quality operations, engineering compliance, and material handling functions.

1. Process Lead – Risk Management (Julphar UAE)

Risk Management is a foundational pillar of global pharmaceutical operations. With advancing regulatory expectations from FDA, EMA, WHO, MHRA, and PIC/S, companies must embed structured risk-based thinking across Quality Management Systems (QMS). Julphar’s Process Lead – Risk Management plays a strategic role in establishing, governing, and strengthening this framework.

Role Overview

The Process Lead – Risk Management is responsible for designing, implementing, and continuously improving the organization’s pharmaceutical risk management framework. The role is deeply rooted in compliance with ICH Q9, Good Manufacturing Practices (GMP), Quality Risk Management, and internal Standard Operating Procedures (SOPs). This professional ensures that risk-based thinking guides decision-making across operations, manufacturing, engineering, quality, and compliance functions.

Key Responsibilities

A. Risk Management Leadership

• Develop and maintain a robust risk management system aligned with ICH Q9 and global GMP principles.
• Lead structured risk assessments such as:
  • Failure Modes and Effects Analysis (FMEA)
  • Fault Tree Analysis
  • Hazard Analysis and Critical Control Points (HACCP)
• Drive risk-based decision-making across CAPA, change control, deviations, validation, and quality system activities.
• Promote risk awareness and structured analysis during manufacturing, engineering & quality operations.

B. Risk Governance and Monitoring

• Maintain site risk registers that track current and potential quality risks.
• Monitor risk mitigation actions and ensure timely execution.
• Establish and review Key Risk Indicators (KRIs) and Key Performance Indicators (KPIs) to measure program effectiveness.
• Lead scheduled risk reviews to assess emerging risks and improvement opportunities.

C. Training & Quality Culture Enablement

• Conduct training on risk assessment tools, methodologies, and GMP-aligned risk processes.
• Mentor cross-functional teams to build a culture of proactive risk identification.
• Reinforce the importance of data integrity, risk visibility, and documentation accuracy.

D. QMS Oversight & Continuous Improvement

• Supervise critical QMS processes including:
  • Deviations
  • CAPA
  • Change Control
  • Documentation
  • Audits (Internal & External)
  • Complaints
• Initiate quality process improvements to enhance compliance and operational efficiency.
• Support Data Integrity initiatives across all systems and records.

E. Strategic & Cross-Functional Collaboration

• Harmonize local procedures with global Quality standards.
• Participate in strategic planning, ensuring risk and quality considerations support long-term business objectives.
• Enable clear communication and alignment between Quality, Production, Engineering, Regulatory Affairs, and Supply Chain teams.

F. Regulatory Compliance

• Ensure compliance with:
  • FDA Regulations
  • EU GMP
  • WHO TRS guidelines
  • Corporate quality standards
• Support audit readiness and regulatory inspection expectations.

Core Competencies Required

• Excellent knowledge of ICH Q9 & Quality Risk Management.
• Strong understanding of global GMP regulations.
• Leadership and cross-functional collaboration.
• Analytical & problem-solving expertise.
• Lean / Six Sigma continuous improvement mindset.
• Strong communication and documentation skills.

Qualifications

• Bachelor’s degree in Pharmacy (mandatory).
• Master’s degree or certifications in Risk/Quality Management preferred.
• Minimum 7 years of experience in pharmaceutical QMS and Risk Management.

Apply

https://careers.julphar.net/job/Ras-Al-khaima-Process-Lead-Risk-Management/732559622/

2. Manager – Quality Control (QC Manager, Julphar UAE)

The Quality Control (QC) department plays a critical role in ensuring that raw materials, in-process samples, and finished products meet strict pharmaceutical standards. The QC Manager at Julphar is a central leader responsible for managing chemical and microbiological laboratories.

Main Purpose of the Role

The QC Manager ensures that Quality Control operations comply with GMP, GLP, analytical procedures, stability program requirements, and regulatory expectations. The role ensures batch release readiness, laboratory data accuracy, timely investigations, and alignment with global regulatory standards.

Key Responsibilities

A. Laboratory Operations Management

• Oversee chemical & microbiological laboratory operations.
• Ensure timely sampling, testing, and reporting.
• Review and approve analytical results, stability studies, and reports.
• Ensure accurate execution of method validation, method transfer & analytical operations.

B. Stability Program Oversight

• Manage ongoing and commitment stability programs.
• Ensure data compliance with ICH stability guidelines.
• Review stability reports and support regulatory submissions.

C. Regulatory & Audit Readiness

• Ensure laboratories are audit-ready at all times.
• Support internal, external, and regulatory inspections.
• Lead the closure of audit observations with effective CAPA.

D. Investigation Management

• Manage & close:
  • Out-of-Specification (OOS)
  • Out-of-Trend (OOT)
  • Deviations
• Oversee investigation reports, root cause analysis & CAPA implementation.

E. Documentation & Data Integrity

• Ensure data integrity (ALCOA+ principles).
• Review SOPs, protocols, reports, and records for compliance.
• Maintain document control as per regulatory expectations.

F. Cross-Functional Collaboration

• Work with Production, QA, Supply Chain, Regulatory Affairs, R&D, Compliance.
• Support new product development, validation, and technology transfer.

G. Training & Resource Management

• Train QC analysts, supervisors, and new staff.
• Monitor performance and ensure technical competency.
• Plan budgets and optimize lab resources.

Core Competencies

• Leadership in QC Operations
• Deep understanding of GLP, GMP & ICH guidelines
• Strong documentation & audit readiness skills
• Problem-solving & decision-making capabilities
• Excellent communication & cross-functional collaboration

Qualifications

• Bachelor’s in Pharmacy (Master’s preferred).
• 10+ years in QC, with 3–5 years in leadership roles.
• Experience with data integrity, audits & EQMS systems (AmpleLogic).

Apply

https://careers.julphar.net/job/Ras-Al-khaima-Manager-Quality-Control/732561322/

3. Team Leader – Production (OSD Plant, Julphar UAE)

Oral Solid Dosage (OSD) forms are among the most widely manufactured pharmaceutical dosage forms worldwide. The Team Leader – Production ensures efficient manufacturing of tablets, capsules, and coated products.

Job Summary

The Team Leader oversees granulation, compression, coating, and packaging processes. The role ensures compliance with GMP guidelines (WHO, USFDA, MHRA), documentation accuracy, safety, and production efficiency.

Key Responsibilities

A. Production Management

• Supervise OSD production operations.
• Maintain adherence to production schedules.
• Coordinate with Planning & Warehouse to ensure material availability.
• Troubleshoot equipment & process issues and implement CAPA.

B. Compliance & QA Alignment

• Ensure operations comply with cGMP, USFDA, MHRA & WHO guidelines.
• Collaborate with QA for in-process checks.
• Handle batch-related deviations, change controls & investigations.
• Maintain regulatory documentation accuracy.

C. Team Management & Training

• Supervise operators, technicians & junior executives.
• Conduct GMP & SOP training programs.
• Evaluate staff performance and guide improvements.

D. Equipment & Process Optimization

• Monitor calibration & maintenance of OSD equipment such as:
  • FBP
  • RMG
  • Tablet press machines
  • Coating machines
  • Blenders
• Identify process improvement opportunities.

E. Safety & GMP Compliance

• Ensure adherence to safety & environmental guidelines.
• Conduct risk assessments.
• Prevent mix-ups, contamination & handling errors.

F. Regulatory & Audit Support

• Support site audits and inspections.
• Complete BMR, SOPs, and validation documentation.
• Implement corrective actions for audit findings.

Qualifications

• B.Pharm, M.Pharm, M.Sc.
• 6–10 years OSD manufacturing experience.
• Strong understanding of GMP, equipment & documentation requirements.

Apply

Link 1: https://careers.julphar.net/job/Ras-Al-khaima-Team-Leader-Production/732271022/
Link 2: https://careers.julphar.net/job/Ras-Al-khaima-Team-Leader-Production/732271222/

4. Team Lead – QA Engineering Oversight (Julphar UAE)

This role focuses on Engineering Quality Oversight—ensuring that engineering operations comply with GMP, SOPs, equipment qualification principles, and QMS processes.

Key Responsibilities

• Enforce cGMP compliance across engineering activities.
• Monitor QMS activities (Deviations, CAPA, Change Control) on AmpleLogic.
• Act as Quality Manager for engineering deviations.
• Participate in cross-functional deviation investigations.
• Review URS for new equipment to ensure GMP alignment.
• Approve qualification protocols for equipment.
• Review engineering SOPs and ensure compliance.
• Drive continuous improvement for engineering compliance.
• Oversee Overall Equipment Effectiveness (OEE) monitoring.
• Mentor team members and improve their technical capabilities.
• Support new engineering projects and installations.

Core Competencies

• Strong process compliance mindset
• Ownership & accountability
• Ability to lead engineering initiatives
• Solution-oriented mindset
• Expertise in equipment qualification & validation
• Excellent interpersonal & communication skills

Qualifications

• Bachelor’s in Mechanical, Electrical or Mechatronics Engineering.
• 7+ years’ experience in Pharma/Healthcare.
• Knowledge of engineering QMS, compliance & KPI systems.
• Excellent English communication and MS Office skills.

Apply

https://careers.julphar.net/job/Ras-Al-khaima-Team-lead-%28QA-Engineering-oversight%29/732107122/

5. Forklift Driver – Warehouse Operations (Julphar UAE)

Warehouse operations are critical to maintaining GMP compliance, ensuring safe material handling, and preventing mix-ups or contamination. Forklift Drivers play an important role in ensuring the accurate movement, storage, and retrieval of pharmaceutical materials.

Key Responsibilities

• Follow cGMP principles in warehouse operations.
• Safely receive, pick, store & issue raw & packaging materials.
• Maintain warehouse cleanliness & safety compliance.
• Ensure approved procedures & SOPs are followed.
• Perform forklift cleaning & coordinate maintenance.
• Ensure accurate stacking and location tagging.
• Avoid mix-ups between batches & material codes.
• Assist in stock verification & inventory counts.
• Move heavy loads safely & maintain proper documentation.
• Handle GRN label placement and storage movement.

Core Competencies

• Compliance-focused mindset
• Accountability & ownership
• Teamwork & time management
• Discipline & organizational skills

Qualifications

• High school diploma
• Forklift driving license (Electrical or Diesel)
• Basic English communication skills

Apply

https://careers.julphar.net/job/Ras-Al-khaima-Forklift-Driver/732429122/