Associate Scientist, Formulation Development
Postuler »Date: 19 avr. 2026
Lieu: Staouéli, 16, DZ, 16062
Entreprise: Hikma Pharmaceuticals PLC
Location: Algiers, Algeria
Job Type: Full-time
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 Associate Scientist, 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.
Main Responsibilities:
- Execute tech transfer, development, and validation projects from feasibility study through to stability batch placement, ensuring adherence to timelines and budgets
- Monitor project progress closely and ensure all activities are completed according to plan
- Propose solutions to technical challenges related to development and tech transfer activities
- Prepare and manage all required documentation from project initiation to registration file submission
- Conduct investigations in case of issues arising during tech transfer or development phases
- Collaborate with central and local teams from feasibility study to validation batch execution
- Ensure effective cross-functional collaboration to support smooth project execution
- Execute and follow up on SAP-related tasks
- Ensure confidentiality of all R&D projects
- Maintain compliance with EHS (Environment, Health & Safety) and quality standards
- Support continuous and efficient execution of all R&D projects from start to finish
- Perform other related duties as assigned by management
Required Skills:
- Strong analytical and problem-solving skills
- Ability to manage multiple projects and meet deadlines
- Good knowledge of pharmaceutical development and tech transfer processes
- Effective communication and teamwork skills
- Basic knowledge of SAP systems is an advantage
- Understanding of GMP and quality requirements
Academic Background and Knowledge:
- Degree in Pharmacy or Engineering (Biology, Chemistry, or Process Engineering)
- Bachelor’s degree in pharmacy or a related scientific field (master’s degree is preferred)
- 0–2 years of experience in the pharmaceutical industry, preferably in R&D and/or Production
- Knowledge of pharmaceutical development, validation, and tech transfer processes