Associate, Regulatory Affairs
Confirmed on the employer's own hiring board on Oct 25, 2026. First seen by Alion on Sep 10, 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, Regulatory Affairs Associates 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:
- Review and ensure the compliance of regulatory dossiers before submission.
- Prepare, compile, and manage regulatory dossiers for Marketing Authorization Applications (MAAs), renewals, and variations.
- Follow up on submitted dossiers throughout the evaluation process until approval is obtained.
- Work closely with R&D, Marketing, Quality, Production, and Supply Chain teams.
- Review and approve promotional materials from a regulatory perspective.
- Prepare, compile, and manage regulatory dossiers related to parapharmaceutical products.
Qualifications:
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:
- Degree in Pharmacy, Master’s degree in Pharmaceutical Quality Assurance, Regulatory Affairs, or an equivalent scientific field.
- Minimum of 2 years of professional experience in Regulatory Affairs.
Skills
- Autonomy, proactivity, and a strong sense of responsibility.
- Strong analytical skills and attention to detail.
- Flexibility and adaptability.
- Team spirit and ability to collaborate effectively.