Sr. Supervisor, Formulation Development
Confirmed on the employer's own hiring board on Oct 30, 2026. First seen by Alion on Oct 29, 2026.
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