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Job Description
Job Description:
- Formulation Supervisor is responsible for implanting R&D section head instructions for pharmaceutical product development and associated activities
- Developing robust products and processes that are scalable, stable and bioequivalent to the Reference Product.
- The specialist will work with cross-functional departments such as Manufacturing, QA, QC, warehouse, Regulatory Affairs, and Portfolio Management.
Human Dosage Forms
- Solid [Capsules – Tablets (Wet Granulation and Dry) – Coated Tablets (Film Coat and Enteric Coat) – SR Tablets].
- Liquids [Syrup – Suspensions – Drops].
- Parentrals [Ampoules – Vial – Cephalosporin].
- Semi-Solids [Ointments – Creams – Gels – Suppositories}.
- Dry Mixed Powders [Antibiotics for oral suspension – Antibiotics for oral Drops – Sachets].
- Lyophilized Products [Vial].
- Participation in the formulation and preparation of the following
Veterinary Dosage Forms
- Solid [Bolus Tablets].
- Parentrals [Vial – L.A. Vial].
- Dry Mixed Powders [W.S.P. – Premix].
- Liquids [Oral Solutions – Suspensions].
- Development and Maintenance of documentation system in R&D department.
- Training of employees in R&D department (GMP and On Job).
- Responsible for Production Scale up of Pilot Batches including the following production areas:
- Semi-Solids Production Area.
- Liquid dosage forms Production Area.
- Solid dosage forms Production Area.
- Sterile Area.
- β - Lactam Area.
Job Requirements
- Sc. in Chemistry or B.Sc. in Pharmaceutical Sciences
- Collecting different data about APIs and Excipients involved in new products.
- Participation in the formulation and preparation of the following