Manufacturing Process Engineer II

Work Schedule

First Shift (Days)

Environmental Conditions

Office

Job Description

Manufacturing Process Engineer II

When part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer and protecting the environment. The work we do has real-world impact, and you'll be supported in achieving your career goals.

How will you make an impact?

Being will be part of the manufacturing engineering team to develop new manufacturing processes that support the global network of Thermo Fisher Scientific SUD manufacturing sites. You will be responsible for ensuring process quality, safety, and delivery to product and process requirements and standards.

What will you do?

Have responsibility for supporting and designing new manufacturing processes as well as improvements to existing processes to improve productivity, capacity, cost reduction, and efficiency. You will support complex projects, support process scale-up, and contribute as a process resource across cross-functional teams.

How will you get here?

Education

• Technical/Engineering Bachelor's degree with at least 2 years of shown applicable experience in a technical/engineering environment or recent Master's degree graduate.

Preferred:

• Lean Six Sigma Green/Black Belt certification (or equivalent)

Experience

• Experience in the assistance of specification (URS) and qualification (FAT/PV) of manufacturing processes (manual and automated)
• Experience in supporting technical engineering efforts thru process design and development projects
• Experience in giving to projects working within multi-functional teams while leading and delivering to individual tasks and efforts
• Experience with engineering tools and methods for tasks such as experimentation (DOE), risk assessment (FMEA), process reliability (SPC, Cpk, MSA), and statistical analysis
• Experience in process design to applicable international standards (e.g. ISO, CE, FDA, etc.) desired

Knowledge, Skills, Abilities

• Experienced in MS Office and MiniTab (or equivalent)
• Lean Manufacturing and Six Sigma methodology
• Understanding of process capability (Cp, Cpk) and reliability (SPC, MSA)
• Experienced 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 demonstrated history of continuous improvement and drive for results

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

Apply today!

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.