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:

• Performing stability, validation, raw materials, packaging materials, semi-finished and finished products analyses.
• Conducting both manual and automated analyses.
• Calibrating and adjusting laboratory equipment.
• Preparing and storing reagents in accordance with established procedures.
• Following the analysis schedule and comparing results against current standards.
• Identifying anomalies and contributing to their resolution.
• Recording and verifying results, and issuing analysis reports.
• Proposing improvements in equipment organization.
• Ensuring maintenance of workstations and providing technical training to new team members.

Qualifications:

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

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

• Skills:

Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).

Familiarity with laboratory equipment and IT systems.

Ability to write procedures and reports.

Strong organizational skills and attention to detail.

• Personal Qualities:

High level of accuracy and attention to detail.

Team spirit with the ability to collaborate across departments (logistics, production, quality assurance, maintenance).

Autonomy and proactive mindset.