Title:  Specialist, Analytical Research

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 Specialist – Analytical Research (R&D) 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:

• Plan and organize analytical activities within R&D projects, including analytical method development, validation, and stability studies.
• Develop, optimize, and validate analytical methods for new products and products under development in accordance with regulatory requirements.
• Prepare and review protocols, reports, and scientific documentation related to analytical validation and stability studies.
• Supervise AR laboratory analysts, organize team activities, and provide daily technical guidance and training.
• Ensure the quality and integrity of analytical data generated in support of pharmaceutical development projects.
• Ensure timely execution of analytical validation and stability programs related to R&D activities.
• Lead or support investigations related to atypical results (OOS, OOT) within development activities.
• Collaborate with Formulation Development, Regulatory Affairs, and Quality teams to support product development and registration.
• Contribute to continuous improvement initiatives to enhance analytical methods and laboratory processes.

Qualifications:

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

• Education: Pharm.D or Master’s degree in Pharmacy, Chemistry, or a related scientific field.
• Experience: Minimum 5 years of experience in Analytical Research or analytical development within the pharmaceutical industry.

Skills:

• Strong knowledge of GMP, ICH guidelines, and regulatory requirements.
• Experience in analytical method development and validation in an R&D environment.
• Ability to supervise a team and coordinate AR laboratory activities.
• Strong analytical mindset, scientific rigor, and innovation orientation.
• Team-oriented with the ability to work in a project-driven environment.