Process Engineer III at Boston Scientific Corporation Malaysia
Cluain Meala, Munster, Ireland -
Full Time


Start Date

Immediate

Expiry Date

08 Apr, 26

Salary

0.0

Posted On

08 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Process Improvement, Technical Expertise, Project Management, Quality Systems, Documentation, Problem Solving, Communication, Team Collaboration, Analytical Skills, Decision Making, Manufacturability, Training, Patient Safety, Product Quality, Engineering, Science

Industry

Medical Equipment Manufacturing

Description
Evaluate process capabilities and identify opportunities for improvement across multiple, moderately complex processes. Apply technical expertise to design, develop, and implement new processes, procedures, tooling, and automation. Deliver on functional requirements related to Product/Technology Development Processes, Project Management, and Quality Systems. Prepare and present technical data and recommendations for review. Author validation protocols and reports for new processes. Ensure all documentation meets quality system standards (e.g., BOMs, Routers, FMEAs). Oversee development builds and coordinate special work requests. Functional Knowledge: Solid understanding of technical concepts and procedures within own function; basic awareness of related functions. Business Expertise: Understand business drivers and collaborate effectively with other teams. Leadership: No direct supervisory duties; may provide informal guidance to new team members. Problem Solving: Address issues using established practices, practical experience, and sound judgement. Impact: Influence the quality and effectiveness of the immediate team and related groups. Communication: Present complex information clearly to internal audiences and support informed decision-making. Provide Design for Manufacturability (DFM) input to engineering packages. Contribute to intellectual property submissions. Train and guide technicians; support manufacturing personnel training as required. Participate as a core or extended team member on new product projects. Demonstrate a strong commitment to patient safety and product quality by adhering to the Quality Policy and all documented quality procedures. Hons bachelor's degree or higher in relevant Engineering / Science field. Minimum of 3+ years' experience within a manufacturing environment. Excellent interpersonal and communication skills. Ability to work as part of a team and meet targets/goals efficiently. Excellent analytical and problem-solving skills. Demonstrated decision making skills.
Responsibilities
Evaluate process capabilities and identify opportunities for improvement across multiple processes. Author validation protocols and reports for new processes while ensuring documentation meets quality system standards.
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