Sr. Supervisor, Formulation Development
تفاصيل الوظيفة
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 Developmentto 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
هذا الإعلان منشور على بيت.كوم المغرب ويُعرض هنا مع الإشارة إلى المصدر. لا نتقاضى أي رسوم من الباحثين عن عمل. إذا كان الإعلان مسيئًا أو احتياليًا، أبلغنا.
