Manager, Manufacturing Engineering

4 days ago


Logan, United States Thermo Fisher Scientific Full time

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

How will you make an impact?

You will lead the manufacturing process engineering team to design and develop manufacturing processes that support a network of Thermo Fisher Scientific SUD manufacturing sites.  You will use data to identify and support continuous process improvement while ensuring design quality, employee safety, and project delivery.

What will you do?             

You will have direct responsibility for the engineering resources and processes related to specifying and qualifying new manufacturing processes as well as process improvements designed to improve productivity, capacity, cost reduction, and efficiency.  You will be responsible to develop your team to ensure high levels of quality and intensity in their work.

How will you get here?
Education
  • Technical/Engineering Bachelor’s degree with 8 years (or Master’s degree with 6 years) of applicable experience including management of engineering resources in a technical/engineering environment.

  • Six-Sigma Black Belt preferred.

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

  • Leading technical engineering teams thru process design and development projects

  • Establishing and using key measures for engineering work (e.g. design quality)

  • Engineering resource forecasting and leading limited resources 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 other statistical software)
  • 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 strong drive for results

At Thermo Fisher Scientific, each one of our 70,000 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.

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.



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