Manufacturing Engineer II (TAS)

Terumo Aortic; Florida; Presencial; USD 95.000 - 130.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual bonus

Paid vacation

Paid holidays

Health benefits

Dental benefits

Vision benefits

401(k) with matching

Descripción de la vacante

Terumo Aortic in Sunrise, FL is seeking a seasoned Manufacturing Engineer to drive process/tool/gauge development and cost reduction. You will document manufacturing methods, support design transfers, and execute validations across the production floor.

The role requires hands-on engineering of tooling and fixtures, with Lean manufacturing and quality system focus. It offers a collaborative environment with growth opportunities and competitive benefits in the Florida market.

Formación

• 5+ years in a technical role in the medical device industry.
• Experience with polymers, medical grade metals and medical packaging.
• Hands-on knowledge of electronics, motion control, plastics, metallurgy and manufacturing processes.

Responsabilidades

• Perform process, tool, and gauge development and implementation activities; implement cost reductions; develop process layouts; maintain manufacturing instructions and device history records; execute process validation protocols, builds and reports.
• Work with engineering director to determine projects and related tasks; refine manufacturing processes and flow; develop new processes to increase productivity and reduce cost.
• Implement cost reductions via materials or manufacturing time; investigate and provide engineering support to Manufacturing processes, SPC, and NCR; prepare, analyze, and present data at monthly NCR and Management Review meetings.
• Manage Tooling System including preventive maintenance, calibrations, and equipment records; manage duties of engineer/technician/intern; complete investigation, improvements and documentation of CAPAs.
• Utilize Lean Manufacturing principles to increase productivity; implement new processes and issue process validation protocols and reports.
• Develop, document (AutoCAD / SolidWorks), and implement fixtures, jigs, tools, and gages; document methods for manufacturing and inspection.
• Work with Research and Development and Process Development to develop and transfer new designs to manufacturing; lead and manage design transfer projects.
• Initiate process, design, and documentation changes through the change management process; utilize statistics for experiments and validations.
• Log engineering evaluations into Engineering Notebooks; perform tooling verifications and IQ/OQ/PQ activities; perform root cause investigations and implement solutions.

Conocimientos

Communication

Software literacy

Experiment design

Problem solving

Tooling fixtures

Prototype development

LSO certification

Herramientas

AutoCAD

SolidWorks

Descripción del empleo

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Department: TAS Manufacturing Engineering

At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to find the right fit for each patient anatomy.

The company has over 1,250 associates around the world with manufacturing facilities in Glasgow, Scotland and Sunrise, Florida

Terumo Aortic is focused on the continuing development of new and innovative products driving the growth of the business globally. Associates are part of a stimulating and exciting environment in which they can develop their skills and achieve career goals. Working for the company, each associate’s role contributes greatly to helping to save or improve the lives of patients in over 100 countries worldwide

At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients

Join us and help shape wherever we go next!

Performs process, tool, and gauge development and implementation activities, implement cost reductions, develop process layouts, develop, and maintain manufacturing instructions and device history records, and execute process validation protocols, builds and reports.

• Work with engineering director to determine projects and related tasks.
• Refine manufacturing processes and flow.
• Develop new processes that increase productivity and reduce cost.
• Implement cost reductions via materials or manufacturing time.
• Investigate and provide engineering support to Manufacturing processes, SPC, and non-conforming material (NCR)
• Prepare, analyze, and present data at monthly NCR and Management Review meetings (if applicable)
• Manage Tooling System including preventive maintenance, calibrations, and equipment records (if applicable)
• Manage duties of engineer/technician/intern, including workload and personal issues (if applicable)
• Complete investigation, improvements, and documentation of preventative and corrective actions (CAPAs)
• Utilize Lean Manufacturing principles to increase productivity / throughput, reduce cost, and /or eliminate waste.
• Implement new processes and issue process validation protocols and reports.
• Develop, document (using AutoCAD / SolidWorks), and implement fixtures, jigs, tools, and gages.
• Document methods for manufacturing and inspection (Manufacturing Instructions)
• Work with Research and Development and Process Development to develop and transfer new designs to manufacturing (lead and manage design transfer projects)
• Initiate process, design, and documentation changes through the change management process
• Utilize statistics to evaluate, justify, and support experiments, analysis, and validations.
• Log engineering evaluations into Engineering Notebooks
• Perform tooling verifications and carry out IQ/OQ/PQ activities.
• Perform Root Cause Investigations, develop and implement solutions.
• Perform process development and execute DOE’s (Design of Experiments)
• Work with Mfg. Supervisor to analyze Manufacturing data and lead improvement projects that come from this analysis.

Job Responsibilities (continued)

Working Conditions/Physical Requirements

Quality Requirements:

Maintain awareness of the relevance and importance of activities performed and how they contribute to the achievement of quality objectives.

Work within the QMS always, ensure accurate completion of records and highlight issues to immediate supervisor any issues affecting quality.

Responsible to ensure facility, processes and documentation always remain in a state of audit readiness.

EH&S requirements:

• Take care of your own health and safety and that of others who may be affected by your actions.
• Work co-operatively to highlight issues affecting Environmental Health and Safety

Knowledge, Skills and Abilities (KSA)

• Excellent written and verbal communication skills
• Proficient in software applications
• Ability to organize and conduct experiments independently.
• Ability to analyze and solve technical problems.
• Hands on abilities to engineer tooling, processes, and equipment.
• Hands on experience building prototypes, tooling, and fixtures.
• If acting as Laser Safety Office (LSO) - Certification of Laser & X-ray safety

Qualifications/ Background Experiences

• 5+ years of experience in a technical role in the medical device industry
• Project management experience in the medical device industry
• Hands-on knowledge of electronics, motion control, plastics, metallurgy, and manufacturing processes
• Experience with polymers, medical grade metals and medical packaging

It is Terumo’s policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.

Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program.

Nearest Major Market: Fort Lauderdale
Nearest Secondary Market: Miami