Job Description

Location: Amman, Jordan

Job Type: Full-time

Hashtag: #LI-OS1

About Us

For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,400+ empowered colleagues are central to this mission.

As a trusted and reliable partner of over 825 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 3 R&D hubs across MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.

We are looking for a talented QA Engineer to join us. At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We’re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.

If you want to be part of a team that cares about impact, this is the place for you.

Key Responsibilities:

• Conduct daily rounds in production to ensure compliance with cGMP.
• Inspect equipment for cleanliness, calibration, and condition.
• Ensure availability and compliance of documentation related to manufacturing.
• Review and verify manufacturing batch records and machine logbooks.
• Monitor employee behavior and compliance with SOPs and process parameters.
• Perform sampling of finished products and verify packaging and labeling.
• Check release requirements of intermediates, and APIs.
• Conduct physical checks and reconciliation of final products.
• Manage QA responsibilities in warehouse, engineering, and production areas.
• Handle pharmaceutical tailing waste and manage QA quarantine area.
• Perform, trend environmental monitoring reports, and ensure compliance.
• Prepare required reports (daily, weekly, monthly, etc.).
• Handling the quality investigations in all operation and R&D departments through manage the investigations and review the final records.
• Perform additional tasks assigned by the department manager.

Qualifications:

We are looking for candidates whose experience and skills align closely with the qualifications outlined below:

• Education: Bachelor’s degree in chemical engineering, or any related field.
• Experience: 1–3 years of experience in a quality assurance or related role.
• Skills:

Preferred qualifications:

• Knowledge of cGMP and regulatory compliance in pharmaceutical manufacturing.
• Strong attention to detail and analytical skills.
• Ability to work in shifts and adapt to changing workloads.
• Good communication and interpersonal skills.
• Proficiency in documentation and report writing.
• Basic knowledge of sampling techniques and environmental monitoring.
• Team-oriented with a proactive approach to problem-solving.
• Very good level in English (Writing, Listening & Speaking).

Learn more about Hikma in Jordan https://www.hikma.com/media/jukhqqdl/hikma-jordan-factsheet_-en-nov-2025.pdf