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Key Responsibilities:
Collaborate with engineers and production teams to develop and improve manufacturing processes.
Develop and implement manufacturing systems and strategies to achieve cost, quality, and time objectives while scaling up output to meet required annual growth rates.
Lead automation initiatives, from conceptual design through implementation, ensuring seamless integration with existing manufacturing processes and full compliance with quality and regulatory standards
Identify and drive implementation of process improvements using Lean methodologies.
Apply structured problem-solving techniques to process, material, or equipment issues, offering manufacturing or quality solutions from experience.
Develop and maintain operational processes and procedures that reflect industry best practices and comply with relevant regulatory requirements.
Perform process analysis and identify areas for improvement, including the evaluation and implementation of automation technologies (e.g., vision systems, robotics, digital monitoring) to enhance productivity, efficiency, and process reliability.
Develop complex experiments and validation protocols; analyse results, make recommendations, and prepare technical reports.
Analyse and resolve complex manufacturing and compliance issues (e.g., CAPA, non-conformances, audit observations).
Develop training materials and documentation (e.g., work instructions) to ensure effective knowledge transfer to production teams.
Work with internal stakeholders to explore and assess new technologies in terms of performance, cost, and reliability.
Actively engage in and support daily manufacturing operations.
Key Requirements:
Level 8 degree in Engineering or related discipline, with 5plus years of relevant experience.
Green Belt certification is a distinct advantage.
Proven experience in medical device process development, manufacturing, and project/program management.
Strong skills in risk analysis, problem-solving, and process validation (equipment and manufacturing).
Dynamic team player with proactive ownership of tasks and projects.
Excellent organizational and interpersonal skills.Solid understanding of Lean principles and tools (e.g., DMAIC, Kaizen, Value Stream Mapping).
In-depth knowledge of ISO 13485 and FDA regulatory requirements. xcfaprz
Proficiency in statistical techniques (e.g., DOE, Six Sigma).
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Sprachkenntnisse
- English
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