Engineer 3 - Manufacturing Equipment Automation

Requisition ID:  32506  

 

At Terumo Blood and Cell Technologies, our 7,000+ 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.

Senior level engineering position providing technical support for development and qualification of automated manufacturing systems for a medical device company.  Position is expected to provide direction to resources internal and external to the organization while mentoring junior engineers and technicians.  Responsibilities include gathering requirements from internal customers, interfacing directly with machine integrators and ensuring system performance meets customer requirements.  Quick learner candidate is best suited for success with common activities including documentation of system requirements, oversight of machine build, acceptance testing, installation and debug, modification of machine control software, HMIs and data collection networks, qualification at site location and providing post validation production support.  Engineering resources will be working within a cross functional matrix, based in Denver Colorado, requiring travel to domestic and/or international machine integrators.

 

ESSENTIAL DUTIES

• Design, installation and validation of automated systems for medical device manufacturing in a clean room environment.
• Development and execution of commissioning (FAT and SAT) protocols and reports
• Assumes accountability for delivery of complete manufacturing systems; starting with design inputs, concluding with design transfer.
• Maintains knowledge of latest technology and design practices to keep organization current with industry development.
• Perform independent evaluation, selection, and application in making adaptations and modifications to projects.
• Assigned total project leadership responsibilities of major capital projects.
• Provides leadership for the functional group’s development, direction, and effectiveness, adhering to organizational policies and processes and supporting overall business and corporate objectives.
• Implements and understands FDA or regulatory requirements as necessary.
• Highlights risks and understands how to complete tasks, avoiding serious delays and considerable expenditure of time and resources.                  
• Advises team members pro-actively on technical ideas and promotes skill development of team work.
• 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.
• 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.

 

MINIMUM QUALIFICATION REQUIREMENTS

Education

• Bachelor’s degr