Manufacturing Engineer II - Electrophysiology

卡塔戈, 哥斯达黎加

申请

贺利氏医疗技术

职位 ID 59986 职能领域 生产运营 全职/兼职 全职 经验水平 专业人士

Manufacturing Engineer II - Electrophysiology

Permanent

About Heraeus

Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead.

About Heraeus Medevio

Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds.

To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today.

JOB PURPOSE

Execute manufacturing engineering actions, projects and investigations assuring the sustaining of production lines according to quality compliance regulations.

MAJOR RESPONSIBILITIES

Execute projects with more complexity to support manufacturing production needs or new products transferred to the production area.
Communicate and get support from different areas assuring that production runs without interruptions and products and processes improvements are alignment with standards and quality system.
Implement engineering tools (Six Sigma DMAIC, DOE’s, Lean) to assure the problem solving, decision making and continuous improvement.
Perform the documentation and records, after production release assuring the manufacturing and quality regulations
Perform the validation process of the projects to accomplish whit the quality regulation for products and processes
Assures that production lines output meets the specifications of the product to have clear criteria of conforming/ non-conforming product and the test methods used for verifying conformance.
Provide information during audits to demonstrate the compliance of quality regulations.
Promote continuous improvement in products and processes to reduce the risks of interruptions in production or quality regulations; it includes implementation of business initiatives.

KNOWLEDGE, SKILLS AND ABILITIES

Engineering bachelor's degree or related.
3 to 5 years of experience in similar positions.
3 to 5 years in medical cluster.
Validation manufacturing process experience is a plus.
Critical Thinking/Analytical Skills.
Excellent bilingual (English/Spanish) verbal and writing.
Normative ISO13485 Knowledge.
Lean and six sigma knowledge.
Knowledge in CAPEX, Budget control and COGS.
Software: AutoCAD & SolidWorks (nice to have).
Promote continuous improvement.
Processes and root cause problem solving methodologies.
Attention to details.
Transfer Process and continuous Improvement Projects implementation experience is desirable.