MAIN RESPONSIBILITIES
- Perform al IPQA (in-process - Quality Assurance) functions
- Be able to perform incoming and outgoing inspections of finished product batches.
- Follow written , approved procedures to maintain cGMP standards.
- Inspect and evaluate procedures and processes for production.
- Participation in validation and qualification activities and preparation of their documents
- Analyze data, create reports and communicate feedback.
- Deliver Training to production teams to reduce quality problems and increase understanding of quality goals.
- Document current state, risks, and process improvement goals.
- Ensures compliance with cGMP, Company SOPs and regulatoryrequirements during all phase of operations.
- Performs process checks and verification's to ensure the quality is maintained.
- Studies product specifications.
- Samples bulk and finished products.
- Monitors all manufacturing processes.
- Reviews all the documentation related to product manufacturing.
- Analyzes quality assurance data.
- Compiles periodical reports.
B.Sc in Pharmaceutical Sciences or Sciences Chemistry is a mustNot less than 7-10 Years of professional experience in the same industry.Ability to understand and comply with GMP. Preferably good chemistry knowledge and analytical chemistry lab experience.Computer operation ability is an asset.