Engineer 5 - Principal Automation Manufacturing

Requisition ID:  32086  

 

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.

 

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.

 

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. Consider joining our team and unlock your potential. 

As a Principal Automation Engineer you will lead cutting-edge projects and shape the future of automation technology. In this pivotal role, you'll leverage your extensive experience in automation frameworks, system integration, and process optimization to drive efficiency and excellence across our operations. Collaborate with cross-functional teams to design and implement sophisticated automated solutions, while mentoring and guiding a talented group of engineers. If you have a passion for innovation, a track record of successful automation projects, and a desire to make a significant impact then we invite you to apply. 

 

ESSENTIAL DUTIES

• Leads and is accountable for projects and drives data based results.
• Lead teams, initiatives and support for highly automated manufacturing work cells that produces parts on a 24/7 basis.  
• Guides the successful completion of major programs and may function in a project leadership role. Erroneous decisions or recommendations would typically result in failure to achieve major organizational objectives.
• Directs one or more major phases of complex engineering work, utilizing engineering skills to devise entirely new approaches to problems encountered in projects.
• Work with global engineering teams to drive continuous improvement projects and improve the Overall Equipment Effectiveness (OEE) across manufacturing lines.
• Develops new processes that have a significant impact on multiple disciplines.
• Contributes to the establishment of business objectives, goals, budgets and costs as requested.
• Presents complex technical information/analysis, and responds to questions from technical staff members and management regularly and effectively.
• Mentors less experienced engineers.
• Provides broad-based direction for subordinates and colleagues within functional area and cross functionally.
• Applies technical expertise to complex tasks with in-depth knowledge of related work areas.
• Employs in-depth knowledge of cross functional and related technical areas, applying knowledge to other areas.
• Displays accessibility and sought out for consultation on a broad range of complex technical and industry issues engineering staff and management.
• Works on complex issues where analysis requires an in-depth evaluation of variable factors. Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results.
• Keeps updated on recent technical advances within the industry and applies this knowledge to products and processes.

• Work may include directing technicians and junior engineers.
• May work with manufacturing and other functional groups on manufacturing and regulatory compliance issues.
• May contribute to the establishment of business objectives, goals, budgets and costs.
• Assesses schedule requirements and plans ahead for a comprehensive solution to complex interdisciplinary issues I projects.
• Acts as a Subject Matter Expert (SME) where skill sets make it appropriate.

 

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's of Science degree or Master of Science degree in Engineering preferred.

 

Experience

• Minimum 8 years experience in an FDA regulated environment including new equipment documentation, process and equipment validations, and continuous improvement identification and implementation.
• Two years of Good Manufacturing Practice (GMP) experience required.
• Must have familiarization with engineering methods, independent thinking, and company practices and policies.

 

Skills

• Requires demonstrated skills in technical innovation, technical Leadership, mechan