Manufacturing and Quality Managers

دوام كامل في Client of Aurawoo International في UAE
نُشرت يوم February 7, 2025

تفاصيل الوظيفة

Summary : The Manufacturing and Quality Manager in the science and pharmaceutical industry is responsible for overseeing the manufacturing processes and ensuring adherence to quality standards, regulatory requirements, and safety protocols. They play a crucial role in managing the production operations, ensuring product quality, and driving continuous improvement initiatives. Key Responsibilities:

  1. Oversee the manufacturing operations, including production planning, scheduling, and resource allocation.
  2. Ensure compliance with regulatory requirements, quality standards, and safety protocols in manufacturing processes.
  3. Develop and implement manufacturing strategies, policies, and procedures to optimize productivity and efficiency.
  4. Manage and coordinate cross-functional teams involved in manufacturing, including production, engineering, and quality assurance.
  5. Monitor production metrics, track key performance indicators (KPIs), and implement corrective actions to improve performance.
  6. Conduct regular quality audits, inspections, and process reviews to ensure product quality and adherence to specifications.
  7. Identify and implement continuous improvement initiatives to enhance manufacturing processes, reduce costs, and increase efficiency.
  8. Collaborate with suppliers and vendors to ensure the availability of quality raw materials and components.
  9. Develop and maintain strong relationships with regulatory authorities and participate in regulatory inspections and audits.
  10. Lead and train the manufacturing team, providing guidance, coaching, and support to ensure high performance and employee development.
Desired Candidate Profile Requirements: Bachelor's or master's degree in a relevant field, such as pharmaceutical sciences, engineering, or quality management. Proven experience in manufacturing and quality management, preferably in the science and pharmaceutical industry. Strong knowledge of manufacturing processes, quality control principles, and regulatory requirements. Familiarity with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards. Excellent leadership and communication skills to effectively manage cross-functional teams and stakeholders. Strong analytical and problem-solving skills to identify and resolve manufacturing and quality-related issues. Proficiency in using quality management systems, data analysis tools, and process improvement methodologies. Knowledge of Lean Six Sigma principles and experience in implementing process optimization projects. Ability to prioritize tasks, manage multiple projects, and deliver results within specified timelines. Strong attention to detail and commitment to ensuring product quality and safety. Familiarity with manufacturing software and systems for production planning and control. #J-18808-Ljbffr

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