Engineer III, Manufacturing Engineering

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

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 is a position in 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 as well as quantifying process capabilities.

How will you get here?

Education

• Bachelor's degree (BSME preferred) with 5 years applicable experience
• OR, Master's degree (MSME preferred) with 3 years applicable experience
• OR, minimum of 12 years applicable technical experience

Demonstrated Experience

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