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Jr. Specialist - QA - Job Opportunity at Julphar

Ras al-Khaimah, AE
Full-time
Entry-level
Posted: July 10, 2025
On-site
AED 60,000 - 80,000 per year (USD 16,000 - 22,000). This estimate reflects entry-level pharmaceutical QA positions in the UAE market, considering the 0-2 years experience requirement and the specialized nature of pharmaceutical quality assurance. Salaries in the region vary based on company size, with multinational pharmaceutical companies typically offering higher compensation packages including benefits.

Benefits

Comprehensive culture transformation program fostering professional growth and development opportunities
Diversity, inclusion, and equal opportunities initiatives creating an equitable workplace environment
Access to world-class research programs and cutting-edge pharmaceutical development projects
Supportive work environment emphasizing compassion, professionalism, and employee well-being
Professional development through exposure to international audit programs and quality management systems

Key Responsibilities

Execute critical line clearance and release activities ensuring product safety and regulatory compliance according to established Standard Operating Procedures
Conduct strategic in-process quality assessments during manufacturing and packaging operations, maintaining adherence to strict pharmaceutical timelines and quality standards
Maintain accurate batch documentation and process monitoring systems that ensure product integrity and regulatory compliance
Verify material and component compliance with production specifications including BMR, BPR, MFM, MPI, MIV, and Dispensing Sheets to prevent costly manufacturing errors
Ensure comprehensive Good Manufacturing Practices compliance across work areas, including documentation oversight and batch record verification
Monitor environmental conditions and equipment calibration to maintain optimal manufacturing conditions and product quality
Contribute to Annual Product Quality Review preparation, providing critical data analysis for regulatory submissions and continuous improvement initiatives
Participate in internal and external audit programs, representing the company's commitment to quality and regulatory excellence
Lead quality-related investigations including deviation analysis and complaint resolution to maintain product safety and customer satisfaction
Manage Corrective Action and Preventive Action processes within digital systems, driving continuous improvement and risk mitigation

Requirements

Education

Bachelor's Degree in Pharmaceutical or similar

Experience

0-2 year's experience in QA IPC functions

Required Skills

Good on process compliance and good command in English Responsible in approach & high on accountability and ownership Good in Time & Task Management GMP (Good Manufacturing Practices) and science Knowledge Functional Knowledge In-process (Production and Packaging) and Quality Assurance Proficient in MS Office (Word & Excel)
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Industry Trends

The pharmaceutical industry in the Middle East is experiencing significant growth driven by increasing healthcare demand and government initiatives to develop local manufacturing capabilities. Quality assurance roles are becoming increasingly critical as regulatory requirements intensify and companies focus on achieving international compliance standards. The UAE's pharmaceutical sector is particularly expanding as part of the country's economic diversification strategy, creating substantial opportunities for QA professionals. Digital transformation in pharmaceutical manufacturing is driving demand for QA specialists who can work with advanced quality management systems and electronic batch records. The integration of Industry 4.0 technologies in pharmaceutical production requires QA professionals who can adapt to automated monitoring systems and data analytics platforms. Post-pandemic focus on pharmaceutical supply chain resilience has elevated the importance of local quality assurance capabilities. Companies are investing heavily in building robust QA teams to ensure continuous production and regulatory compliance, making entry-level QA positions increasingly valuable for career development.

Role Significance

Typically part of a 5-8 member QA operations team, reporting to QA Team Leaders and working closely with production, packaging, and regulatory affairs departments. The collaborative nature of pharmaceutical manufacturing requires regular interaction with cross-functional teams.
Entry-level specialist position with significant responsibility for product quality and regulatory compliance. Despite being junior-level, the role carries substantial accountability for patient safety and product integrity, making it a critical stepping stone in pharmaceutical quality assurance career progression.

Key Projects

Annual Product Quality Review preparation and analysis Implementation of quality management system improvements Participation in regulatory audit preparations and responses Development of standard operating procedures for new products or processes Quality investigation projects for deviation resolution and process improvement

Success Factors

Strong attention to detail and meticulous documentation practices are essential for maintaining regulatory compliance and preventing costly manufacturing errors that could impact patient safety and company reputation. Ability to work under pressure while maintaining accuracy is crucial in pharmaceutical manufacturing environments where production schedules must be met without compromising quality standards. Continuous learning mindset to stay updated with evolving pharmaceutical regulations, quality standards, and industry best practices in an increasingly complex regulatory environment. Strong communication skills for effective collaboration with cross-functional teams and clear documentation of quality issues and investigations. Adaptability to work with various quality management systems and emerging technologies in pharmaceutical manufacturing.

Market Demand

High demand driven by pharmaceutical industry expansion in the UAE and Middle East region, with particular emphasis on quality assurance roles due to increasing regulatory requirements and the need for local manufacturing capabilities.

Important Skills

Critical Skills

GMP knowledge is absolutely essential as it forms the foundation of all pharmaceutical manufacturing operations and regulatory compliance. Understanding and applying GMP principles ensures product safety, quality, and regulatory approval. Process compliance skills are crucial for maintaining manufacturing standards and preventing deviations that could result in product recalls, regulatory actions, or patient safety issues. Documentation and record-keeping accuracy is vital in pharmaceutical manufacturing where regulatory authorities require comprehensive traceability and accountability for all quality-related activities. Time and task management capabilities are essential for meeting production schedules while maintaining quality standards, as delays in QA processes can impact entire manufacturing operations.

Beneficial Skills

Advanced data analysis skills for trend identification and quality improvement initiatives Knowledge of international pharmaceutical regulations beyond GMP, including ICH guidelines and FDA requirements Experience with additional quality management software platforms and electronic batch record systems Understanding of statistical process control and quality metrics for continuous improvement Project management skills for leading quality improvement initiatives and cross-functional collaboration

Unique Aspects

Opportunity to work with a leading regional pharmaceutical company during a period of significant culture transformation and growth
Exposure to comprehensive pharmaceutical manufacturing operations including both production and packaging quality assurance
Direct involvement in regulatory audit processes and quality management system implementation
Access to advanced quality management systems including Ampelogic platform for CAPA management
Opportunity to contribute to Annual Product Quality Reviews, providing valuable experience in regulatory documentation and analysis

Career Growth

Typically 2-3 years to advance to mid-level QA specialist roles, with potential for team leadership positions within 4-5 years given the growing pharmaceutical sector in the region and increasing demand for experienced QA professionals.

Potential Next Roles

QA Specialist (3-5 years experience) Senior QA Specialist focusing on specific therapeutic areas QA Team Leader or Supervisor positions Quality Manager roles in smaller pharmaceutical companies Regulatory Affairs Specialist positions Quality Assurance Manager in manufacturing operations

Company Overview

Julphar

Julphar is a leading pharmaceutical company in the Middle East and North Africa region, established as one of the largest pharmaceutical manufacturers in the Gulf region. The company focuses on developing and manufacturing high-quality pharmaceutical products across various therapeutic areas, with a strong emphasis on serving the regional market while maintaining international quality standards.

Julphar holds a prominent position in the Middle Eastern pharmaceutical market, with significant market share in the Gulf region and expanding presence across MENA countries. The company is recognized for its manufacturing capabilities and quality standards, making it a respected employer in the pharmaceutical industry.
Based in Ras al-Khaimah, UAE, Julphar operates in a strategic location that serves as a hub for pharmaceutical manufacturing and distribution across the Middle East and North Africa. The UAE location provides access to a skilled workforce and modern infrastructure supporting pharmaceutical operations.
The company emphasizes culture transformation with strong focus on respect, collaboration, innovation, integrity, and compassion. The work environment promotes diversity and inclusion while maintaining high professional standards typical of pharmaceutical manufacturing operations.
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