As a senior manufacturing engineer, you will play a pivotal role in developing and optimising advanced neurovascular medical devices used in the treatment of strokes and aneurysms.
Key Responsibilities:
* Own and sustain manufacturing processes within value streams for Neurovascular products, ensuring product quality, process stability, and regulatory compliance.
The position demands strong emphasis on precision, process reliability, and adherence to stringent regulatory and quality standards.
You will be responsible for driving process efficiency and continuous improvement across all stages of complex assembly operations ensuring validated manufacturing systems consistently deliver exceptional product quality.
This includes executing process changes under Stryker's quality system including documentation risk assessment validation change control supporting ongoing process validation IQ/OQ/PQ maintain validated state through periodic reviews revalidations as required. You'll also partner with Production Quality Maintenance Supply Chain teams improve equipment uptime throughput reliability lead data collection analysis reporting key performance metrics yield downtime cost unit drive improvements findings. Qualifications include Bachelor's degree or equivalent Manufacturing Mechanical Industrial Biomedical Engineering related discipline minimum 2 + years experience regulated medical device high-volume precision assembly environment proven expertise continuous improvement problem solving Lean Six Sigma Green Belt preferred solid understanding manufacturing documentation change control technical judgment hands-on approach resolving engineering challenges excellent interpersonal communication skills influence work cross-functionally #IJ