We’re Hiring R&D Formulation Supervisor, Location: 6th of October City.
Are you passionate about pharmaceutical innovation and formulation development? Join our dynamic R&D team and play a key role in shaping high-quality, compliant, and effective products.
Technical Responsibilities:
- Collect all literatures related to the products of concerns.
- Performing instrument qualification & preparing SOP.
- Performing pre-formulation& formulation trials for any of the new products or the product under redevelopment inside or outside the plant according to the predetermined procedures and after having the necessary training.
- Prepare samples for stability, export & Bio-equivalency studies.
- Documentation and reporting all formulation trials observation and results according to the predetermined procedures.
- Performing pilot trials and validation batches inside and outside directed.
- Complying with the occupational safety and waste procedures in plant.
- Complying with the applicable GMP standards and procedures after having the necessary training.
- Reporting any other event or observation concerning equipment, utility, method, product or procedure and any other relevant item in the R&D department.
- perform any other task related to the job description or nature.
- Performing as second person verification.
- Trouble shooting & process improvement responsibility for running production products.
Report Preparation:
- Preparation of monthly reports to Department Manager.
- Preparation of all documents related to the Product.
Education:Bachelor’s degree in Pharmacy.Master’s degree in Pharmaceutics or Pharmaceutical Technology (preferred).Experience:4+ years of relevant experience in pharmaceutical formulation development.Previous experience in a supervisory or team-leading role within an R&D environment is a strong advantage.Technical Skills:Solid understanding of formulation principles, pre-formulation studies, process development, and scale-up.Hands-on experience with equipment such as: granulators, tablet presses, fluid bed dryers, coating machines, etc.Knowledge of analytical techniques and interpretation of stability and compatibility data.Familiarity with ICH guidelines, GMP, and regulatory filing requirements (e.g. CTD, DMF).Soft Skills:Excellent problem-solving, analytical, and project management abilities.Good communication skills (verbal and written) in English.Additional Requirements:High attention to detail and commitment to documentation and reporting accuracy.Strong organizational skills with the ability to manage multiple projects and deadlines.Up-to-date with new technologies, ingredients, and global trends in pharmaceutical formulation.