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Job Description
- Oversee daily production operations to ensure efficiency, quality, and compliance with safety standards.
- Develop, implement, and optimize manufacturing processes to maximize productivity and minimize waste.
- Monitor and analyze production data, identifying areas for process improvement and cost reduction.
- Collaborate with cross-functional teams including quality assurance, maintenance, and R&D to resolve technical issues.
- Prepare and maintain detailed documentation for production processes, equipment, and quality control procedures.
- Lead root cause analysis and implement corrective actions for production-related problems.
- Support the introduction of new products and technologies into the manufacturing process.
- Train and mentor production staff on best practices, safety protocols, and equipment operation.
- Ensure compliance with regulatory requirements and internal policies related to medical device manufacturing.
- Participate in continuous improvement initiatives such as Lean Manufacturing and Six Sigma projects.
Job Requirements
- Bachelor’s degree in Mechanical Engineering, Industrial Engineering, or a related field.
- 4 to 7 years of experience in a production or manufacturing engineering role, preferably within the medical or pharmaceutical industry.
- Strong understanding of manufacturing processes, equipment, and quality control systems.
- Proven ability to analyze data and implement process improvements.
- Familiarity with regulatory standards relevant to medical device manufacturing (e.g., ISO 13485, GMP).
- Excellent problem-solving skills and attention to detail.
- Strong communication and interpersonal skills for effective collaboration.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
- Experience with Lean Manufacturing, Six Sigma, or similar methodologies is an advantage.
- Proficiency in using production management software and Microsoft Office Suite.
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