#Zeta_pharma is hiring R&D Section Head
Location: Sadat City
~JOB DESCRIPTION:
• Maintain office supply, safety tools and formulation lab requirements available.
• Check the Literature survey for new development products.
• Review the analysis results for compatibility studies.
• Conduct physical and chemical characterization for the Originator.
• Conduct de-formulation testing of originator API and excipients characterization.
• Determine the new API and excipients specification.
• Determine the suitable Formula and manufacturing process technique.
• Perform plan for product development, schedule experiments and prioritize assignments.
• prepare the training program to maintain personnel proficiency and adequate skill levels.
• Identify training needs of subordinates.
• Follow up and check the raw materials availability as per formulation plan
• Follow up material requisition issuing, weighing and receiving from warehouse.
• Check the lab. Scale trial sheet before implementation.
• Follow up pre-formulation compatibility study
testing, formulation trials analysis, lab scale stability testing and pilot scale stability testing.
• Conduct experimentation design for high-risk excipients, formulation, and parameters variables.
• Conduct data analysis and figure out the significant variables.
•Predict the significant variables’ acceptable range and update the risk assessment.
• Recognize, assess, and update the existing process technology to improve the process development capabilities
• Conduct calculation for manufacturing process parameters scaling up.
• Prepare troubleshooting report for assigned production incident.
• Analyze and evaluate the current plant site for
technology transfer feasibility.
• Conduct technical transfer training.
• Coordinate with supply chain, production
department for technology transfer project completion.
• Ensure GMP, GDP, and EHS implementations and update the formulation SOPs.
• Check and update the documents for new products registration requirements.
• Follow up troubleshooting and validation batches incident/ deviation and follow up CAPA implementation.
~JOB REQUIREMENTS:
• Bachelor’s pharmacy, or chemistry.
• Minimum 7 years of experience
• Professional analytical capabilities
• Professional problem-solving skills
~If interested kindly send your cv to
samah.sabry@zetapharma.net
mention your job title in the subject.
