Quality Control Specialist Saudi National

• Monitor and maintain the quality standards of the production process ensuring adherence to regulatory guidelines and industry standards.
• Conduct routine inspections tests and audits to verify the quality of raw materials inprocess materials and finished products.
• Develop and implement quality assurance plans to identify any discrepancies or qualityrelated issues and recommend corrective actions.
• Oversee the daily production processes ensuring they are operating smoothly and efficiently.
• Optimize production methods to improve yield reduce waste and enhance overall production efficiency.
• Troubleshoot production issues ensuring that any interruptions or inefficiencies are addressed promptly.
• Maintain accurate records of production and quality data for compliance with internal and external audits.
• Ensure that all production practices comply with health safety and environmental regulations.
• Prepare reports detailing product specifications testing outcomes and production metrics.
• Work closely with R&D engineering and production teams to align on product specifications and improvements.
• Provide technical support and guidance on product development and production scaling.
• Participate in regular meetings to discuss quality improvements and process optimizations.
• Stay updated on industry best practices and emerging technologies in the quality control and production management fields.
• Lead or contribute to continuous improvement projects focusing on enhancing production efficiency and reducing costs.
• Assist in the implementation of new technologies or production techniques that may improve product quality or increase productivity.
• Provide training and mentorship to junior staff members or new hires on quality control and production processes.
• Ensure that all team members are wellversed in standard operating procedures (SOPs) and quality guidelines.

Qualifications :

• A Bachelors degree in Pharmacy Chemistry Industrial Engineering Chemical Engineering Microbiology Biochemistry or Biomedical Engineering.
• Experience:
• 03 years of experience in a quality assurance or production role within a manufacturing pharmaceutical chemical or biotech industry.
• Experience with quality management systems (QMS) and regulatory compliance (e.g. ISO GMP SFDA).

Remote Work :

No

Employment Type :

Fulltime