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 Validation & Stability Officer 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:

Performing stability, validation, raw material, packaging material, in-process, and finished product analyses. Carrying out manual and automated analytical tests. Calibrating and adjusting laboratory equipment. Preparing and storing reagents in accordance with established procedures. Adhering to analysis schedules and comparing results with applicable specifications. Detecting deviations and contributing to their investigation and resolution. Recording and verifying results and issuing certificates of analysis. Proposing improvements related to laboratory equipment organization. Ensuring proper maintenance of workstations and providing technical training to new team members.

 

Qualifications:

Bachelor’s degree (Bac+3/4) in Chemistry, Pharmaceutical Analysis and Quality Control, or equivalent.

Key Skills:

Good knowledge of GMP and GLP. Familiarity with laboratory equipment and computerized systems. Ability to write procedures and technical reports. Strong organizational skills and attention to detail. Strong sense of rigor, autonomy, and priority management.

 

Learn more about Hikma in Morocco hikma-morocco-factsheet-nov-2024.pdf