- Active and inactive ingredients COAs revision and identify require specification
- Reformulation studies.
- Redevelopment of current products if needed in Reregistration status and Follow up all the physical and chemical testing.
- Participating in transforming R&D product development efforts into scalable manufacturing process.
- Assisting in troubleshooting and overcoming productions problems
- Ensuring the implementation of Current Good Manufacturing Processes (cGMP) as well as other set standards to ensure compliance with regulatory requirements.
- Collect all literature related to products of concern.
- 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.
- Reporting any other event or observation concerning equipment, utility, and method.
Bachelor of pharmacy, science and any related studies.Experience: 2-5 years in pharmaceutical industries.Data Analyst, knowledge of Pharmaceutical Processes and is having an analytical thinking.Excellent English written and spoken.Excellent computer skills.Excellent communication and interpersonal skills.