Location: Casablanca, Morocco
Job Type: Full-time
Hashtag: #LI-MM1
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 9,500+ empowered employees are central to this mission.
As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.
Description:
We are looking for a talented , QC Analyst 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:
Perform manual and automated laboratory analyses
Set up, calibrate and operate IPC laboratory equipment
Prepare and store reagents according to established procedures
Follow the planned testing schedule
Record, review and compare analytical results against applicable specifications
Identify deviations or unusual results and support their investigation with the relevant team
Ensure accurate and complete documentation of analytical results
Enter results into analysis reports and related quality documentation
Contribute to improving the organization and use of IPC laboratory equipment
Maintain a clean and well-organized laboratory workspace
Keep accurate equipment records and document relevant equipment activities
Qualifications:
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:
Bachelor’s degree in Chemistry or a related field
Good understanding of Quality Control activities, GMP and GLP requirements
Good communication skills
Good knowledge of laboratory equipment and analytical techniques
Good understanding of regulatory and quality requirements
Organized, detail-oriented and committed to quality