Title:  Sr. Supervisor, Formulation Development

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, Sr. Supervisor, Formulation Development 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:

• Lead technology transfer activities from R&D to manufacturing.
• Oversee process optimization and scale-up activities.
• Plan and manage development projects, timelines, resources, and budgets.
• Work closely with R&D, PMO, Quality Assurance, Production, Regulatory Affairs, and Supply Chain.
• Lead, coach, and develop a team of formulation development professionals.
• Ensure accurate documentation and compliance with cGMP and regulatory requirements.

Qualifications:

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

• Degree in Pharmacy, Chemical Engineering, or a related field.
• 5 to 10 years of experience in pharmaceutical manufacturing or industrial development.
• Experience in technology transfer, process scale-up, and cross-functional project management.
• Strong knowledge of GMP and regulatory requirements.
• Good communication, analytical, and leadership skills.
• Fluent in English and French