Engineer 3 - Global Supplier Quality

Requisition ID:  34502  

 

At Terumo Blood and Cell Technologies, our 8,000+ global associates proud to come to work each day, knowing that what we do impacts the lives of patients around the world. For Terumo, for Everyone, Everywhere.

 

We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and service offerings, we touch a patient’s life every second of every day and are committed to continuing to increase the number of patients we serve. Advancing healthcare with heart.

 

With some of the best and brightest minds in the industry, an unmatched global footprint, comprehensive benefits and a distinct culture, Terumo Blood and Cell Technologies is a great place to work, grow and be part of a team that is focused on making a difference. Join us and help shape wherever we go next. You create your future and ours.

 

As an Engineer 3 - Global Supplier Quality Engineer (SQE), you'll be responsible for working with suppliers to resolve quality issues, improve process reliability, repeatability, and controls.  The SQE must be proficient in tubing/vinyl extrusion, process controls, process validation and verification, technical report writing, CAPA investigations, process improvement and project management.

ESSENTIAL DUTIES

• Functions as a member of the Global Supplier Engineering Team working cross-functionally and proactively on supplier quality and management activities.  These activities include: 

• • Extrusion troubleshooting
  • Component, tooling, and process validations / verification with technical reports
  • Project management of supplier quality initiatives
  • Corrective and Preventative Action (CAPA)

• Highlights risks and understands how to approach and complete tasks, avoiding serious delays and considerable expenditure of time and resources.                  
• Perform independent evaluation, selection, and application in making adaptations and modifications to projects.
• Receives assigned total project leadership responsibilities on a portion of major significant projects and will be given total management responsibility for smaller projects.
• Manages and provides leadership for the functional group’s development, direction, and effectiveness, adhering to organizational policies and processes and supporting overall business and corporate objectives.
• Understands FDA or regulatory requirements as necessary.
• Applies technology principles to multiple tasks. Working knowledge of cross-functional and related technical areas.
• Advises team members pro-actively on technical ideas and promotes skill development of teamwork.
• Interacts with peers across projects to secure resources and commitments.
• Handles frequent inter-organizational and outside customer contacts.  Represents the organization in providing solutions to difficult technical issues associated with specific projects.
• Follows technical specification requirements and provides feedback on various technical processes and procedures.
• Presents effectively complex technical information/analysis and responds to questions from technical staff members and management.   
• Works cooperatively and effectively within a team environment to achieve common goals and results, often influencing the outcome of the team(s).
• Work direction responsibility may include technicians and junior engineers.
• May work with manufacturing and other functional groups on manufacturing and regulatory compliance issues.
• Performs ISO 13485 and or ISO 9001-based audits of suppliers and conducts other assessments of supplier capability.

 

MINIMUM QUALIFICATION REQUIREMENTS

Education

Bachelor’s degree or equivalent of education and experience sufficient to successfully perform the essential functions of the job may be considered.  Bachelor of Science Degree in Engineering, preferred.

 

Experience

• Minimum 4 years experience.
• Two years of GMP manufacturing experience required.

 

Skills