Specialist – Tech Transfer

Job Overview

Julphar is seeking a Specialist – Tech Transfer to join their team in Ras Al Khaimah, United Arab Emirates. This crucial role involves the systematic transfer of technology and manufacturing processes within the pharmaceutical sector, ensuring efficient, compliant, and high-quality production outcomes.

Company Overview

The Julphar story is defined by innovation and leadership in healthcare, beginning in 1980. Headquartered in Ras Al Khaimah, UAE, Julphar has expanded into one of the largest pharmaceutical manufacturers across the Middle East and Africa. The company employs over 3000 people and markets its products in more than 40 countries. With 10 internationally accredited facilities, Julphar produces over one million medicine boxes daily, including various forms of medication and vaccines, maintaining an extensive portfolio of generic, branded generic, and over-the-counter medicines.

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Qualifications: None / Open to all applicants
• Experience: 3 Year+

Key Responsibilities

• Lead and manage the transfer of manufacturing processes and analytical methods from R&D to production.
• Ensure strict compliance with cGMP, regulatory guidelines, and internal quality standards throughout tech transfer projects.
• Develop, execute, and document comprehensive tech transfer protocols, reports, and related procedures.
• Collaborate effectively with cross-functional teams including R&D, production, quality assurance, and engineering.
• Proactively troubleshoot and resolve technical challenges encountered during process scale-up and implementation.
• Conduct thorough risk assessments and implement robust mitigation strategies for all technology transfer activities.

Requirements

• Bachelor’s degree in Pharmacy, Chemical Engineering, Biotechnology, or a closely related scientific field.
• Minimum of 3 years of hands-on experience in pharmaceutical manufacturing, process development, or technology transfer.
• Strong understanding of current Good Manufacturing Practices (c-GMP) and pharmaceutical quality systems.
• Demonstrated excellent project management, problem-solving, and critical thinking skills.
• Exceptional communication and interpersonal abilities for effective team collaboration.
• Proficiency in English is essential; knowledge of Arabic is an advantage.

Benefits

• Opportunity to work with a leading and innovative pharmaceutical manufacturer in the MENA region.
• Engage in impactful projects that contribute to global healthcare advancements and product innovation.
• Competitive salary and a comprehensive benefits package.
• Significant opportunities for professional development and career progression within a growing company.
• A collaborative, dynamic, and supportive work environment.
• Exposure to state-of-the-art manufacturing facilities and advanced pharmaceutical technologies.