Our client is a global leader in Medical Devices, empowering individuals to achieve their fullest health potential.
Key Responsibilities:
* Lead a team of manufacturing operators, providing guidance and support to ensure team effectiveness and productivity.
* Oversight of day-to-day operations within the manufacturing process, including scheduling, resource allocation, and troubleshooting to meet production targets.
* Drive continuous improvement initiatives to enhance process efficiency, quality, and safety.
* Cross-functional collaboration with Quality Assurance, Engineering, and Maintenance to address issues and optimize processes.
* Maintenance of regulatory compliance and company policies, focusing on quality and safety.
Requirements:
* Bachelor's degree in Engineering or a related field.
* 4 years of experience in manufacturing operations, preferably in the Medical Device sector.
* Knowledge of regulatory requirements, including FDA regulations, ISO standards, and cGMP guidelines.
* Experience with continuous improvement methodologies such as Lean Six Sigma preferred.
The ideal candidate will possess strong leadership skills, excellent communication abilities, and a passion for driving process improvements. If you are a motivated professional looking to make a meaningful impact in the medical device industry, we encourage you to apply.