Engineer, QA

About UsFor 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.  

Description: 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– 5 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).