Title:  Analyst, QC

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.