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Manufacturing Engineer, Sr. Staff, Warwick
Client: Confluent Medical Technologies
Location: Warwick, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Reference: b965660184e9
Job Views: 10
Posted: 01.08.2025
Job Description:
Job Description: Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our expertise and partnership with clients allow us to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our capabilities include Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires.
We are looking for a Process Development Engineer, Sr. Staff to join our team. The candidate will be responsible for production planning, inventory control, and leading continuous improvement initiatives to enhance manufacturing efficiency and service levels.
Key Responsibilities:
* Support Lean Manufacturing and continuous improvement programs, utilizing root cause analysis and statistical tools to increase yields and efficiencies.
* Use DOE and other tools to understand and improve performance.
* Troubleshoot machine and process issues with production teams.
* Support product lifecycle changes.
* Perform IQ/OQ/PQ validations for new equipment and products following ISO13485 standards.
* Interact with key customer contacts and engineering staff.
* Collaborate with Quality Assurance to meet requirements and address root causes and corrective actions.
Principal Duties:
* Lead lean manufacturing and CI projects from start to finish, managing improvement teams.
* Develop and monitor metrics for production, and implement process controls to reduce variation.
* Execute IQ/OQ/PQ activities related to new equipment and process improvements.
* Engage with customers, medical device engineers, and quality/regulatory teams.
* Coordinate with vendors, suppliers, and consultants.
Qualifications:
* BSc in Textile Science & Engineering, Material Science, Mechanical, Chemical, Biomedical Engineering, or similar.
* 9-12 years of engineering experience focusing on Lean Manufacturing and CI.
* Familiarity with SolidWorks and CAD preferred.
* Lean and Statistical process certifications required; Green Belt Six Sigma preferred.
* Experience with knitting, weaving, braiding, or non-woven product development is a plus.
* Ability to manage multiple projects simultaneously.
* Knowledge of medical device regulations and ISO13485 preferred.
Other Skills:
* Strong interpersonal, communication, and problem-solving skills.
* Proficient with Microsoft Office suite.
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