Specialist – QA (Sterile)

Job Overview

Julphar is seeking a dedicated Specialist – QA (Sterile) to join their team in Ras Al Khaimah, United Arab Emirates. In this role, you will be crucial in ensuring the highest quality and compliance standards for sterile pharmaceutical products, contributing to better healthcare outcomes globally.

Company Overview

The Julphar story is one of innovation and leadership. Since their journey began in 1980, their goal has remained the same – to bring better healthcare and a brighter future to families across the globe. In less than 40 years, they have expanded their network across the Middle East and Africa to become one of the largest pharmaceutical manufacturers in the region. Headquartered in Ras Al Khaimah in the United Arab Emirates, they employ over 3000 people and market their products in more than 40 countries. They have 10 internationally accredited facilities that produce more than one million medicine boxes a day, including tablets, syrups, suspensions, creams and injectables, and vaccines. Julphar has an extensive portfolio of generic medicines, branded generics, and over-the-counter medicines.

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Qualifications: Bachelor’s Degree
• Experience: 5 Year+

Key Responsibilities

• Ensure strict compliance with GMP, GLP, and quality standards for sterile pharmaceutical products.
• Conduct thorough quality control checks and audits throughout the sterile manufacturing process.
• Investigate any deviations, non-conformances, and out-of-specifications, implementing effective corrective and preventive actions.
• Maintain comprehensive and accurate documentation for all quality assurance activities and procedures.
• Actively participate in and support continuous improvement initiatives aimed at enhancing sterile product quality and processes.
• Collaborate closely with production and other cross-functional teams to uphold product integrity and safety.

Requirements

• Bachelor’s degree in Pharmacy, Chemistry, Microbiology, or a related scientific field.
• Proven extensive experience in Quality Assurance, specifically within a sterile pharmaceutical manufacturing environment.
• Strong understanding and practical application of Good Manufacturing Practices (GMP) and relevant regulatory requirements.
• Excellent analytical, problem-solving, and decision-making skills with keen attention to detail.
• Ability to work effectively both independently and as a collaborative member of a diverse team.
• Proficiency in using quality management systems and other relevant software tools.

Benefits

• Opportunity to work with one of the largest and most innovative pharmaceutical manufacturers in the region.
• Competitive salary and a comprehensive benefits package.
• Significant opportunities for professional growth, development, and career advancement.
• Work in a dynamic, challenging, and innovative environment.
• Contribute directly to improving global healthcare outcomes through quality assurance of vital medicines.
• Access to state-of-the-art facilities and cutting-edge pharmaceutical technologies.