Process Manufacturing Engineer II at Thermo Fisher Scientific in Logan, Utah

Job Description:

Work Schedule

Standard (Mon-Fri)



Environmental Conditions

Office



Job Description



When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals.




How will you make an impact?



This position is part of the Manufacturing Engineering Team which includes process engineers, mechanical engineers, controls engineers, project managers, and engineering technicians. You will focus on developing new manufacturing processes that support a global network of Thermo Fisher Scientific SUD manufacturing sites. You will also focus on supporting site- and network-level process improvement initiatives. You will be responsible for all aspects of this engineering effort including such things as design quality, safety, and delivery.




What will you do?



You will have direct responsibility for the engineering efforts related to specifying and qualifying new manufacturing processes as well as process improvements designed to improve productivity, capacity, waste reduction, and efficiency. This will include things such as creating and maintaining value stream maps and line layouts.




How will you get here?




Education

• Bachelor's degree (BSME preferred) with 3 years applicable experience
  
  


• OR, Master's degree (MSME preferred)
  
  


• OR, minimum of 8 years applicable technical experience
  
  

Demonstrated Experience

• Specification and qualification of manufacturing processes (manual and automated)
  
  


• Contributing to technical engineering teams through process design and development
  
  


• Handling tasks across multiple projects
  
  


• Engineering tools and methods for tasks such as experimentation (DOE), risk assessment (FMEA), process control (SPC), and statistical analysis
  
  


• Design and implementation of automated processes for high-mix/low-volume production desired
  
  


• Process design to applicable international standards (e.g. ISO, FDA, etc.) desired
  
  

Knowledge, Skills, Abilities

• Proficient in MS Office and MiniTab (or equivalent)
  
  


• Proficient in technical writing including authoring engineering protocols, reports, and procedures
  
  


• Medical Device/Biopharmaceutical manufacturing (i.e. GMP, FDA, ISO 13485) experience desired
  
  


• Self-motivated with good problem solving, communication, and coordination skills
  
  


• Self-starter with history of continuous improvement and a strong drive for results
  
  

At Thermo Fisher Scientific, each one of our 120,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer.


Apply today! http://jobs.thermofisher.com


Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Apply Now