- Supervise day-to-day formulation activities in the laboratory and pilot plant.
- Develop and optimize formulations for solid, semi-solid, and/or liquid dosage forms.
- Conduct scale-up and technology transfer to production.
- Ensure compliance with cGMP, GLP, and regulatory requirements (local and international).
- Prepare and review technical documents: batch records, protocols, reports, SOPs, and validation documents.
- Troubleshoot formulation and manufacturing issues.
- Train, mentor, and guide formulation scientists and technicians.
- Support regulatory submissions with technical documentation.
- Collaborate with Quality Assurance and Production to ensure smooth technology transfer.
- Ensure safe handling of chemicals and adherence to EHS (Environment, Health & Safety) guidelines.
Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, or related field (Master’s preferred). 5–7 years of hands-on experience in pharmaceutical formulation development (preferably in solid dosage forms, tablets, capsules, or liquids).Strong knowledge of formulation techniques, excipients, and analytical methods.Proven experience in scale-up, process validation, and technology transfer.Knowledge of international guidelines (FDA, EMA, ICH, WHO).Excellent leadership and team supervision skills.Strong problem-solving, analytical thinking, and communication skills.Proficient in MS Office and formulation software/tools.Ability to work under pressure and meet strict deadlines.Work ConditionsLocation: 10th of Ramadan Industrial Zone.Full-time, on-site.Competitive salary + benefits (to be defined by company).