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Job Description
- Collect all literature related to products of concern.
- Performing instrument qualification & preparing SOP for the instrument.
- 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-equivalence studies .
- Documentation and reporting all formulation trials observation and results according to the predetermined procedures.
- Performing pilot trials and validation batches inside and outside as directed.
- Complying with the occupational safety and waste procedures in Macro Pharma 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.
- To perform any other task related to the job description or nature.
Job Requirements
- B.Sc. degree in Pharmacy
- Data Analysis, Knowledge in Pharmaceutical Processes, Knowledge in Research Methodologies, Analytical Thinking.
- Fluent in English
