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Process Engineer

 

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. 

 

Your Role

 

The Process Engineer 1 is an entry level engineering position responsible for supporting the manufacture and testing of high purity filters, prioritizing safety, and maintaining a focus on quality, process control, electro-mechanical assembly, and material handling. You are responsible for establishing operating specifications and implementing and improving basic manufacturing techniques You will closely monitor the performance of machinery, automated equipment, and tools to verify their efficiency and investigate and initiate corrective action for challenging problems and deficiencies to ensure product quality. This position works with higher level engineers to ensure process stability with a focus on maximizing safety, quality, yields, and productivity and requires collaboration with cross functional team to assess risk, disposition product, and resolve problems. Daily tasks to include the following:

 

  • Maintains efficiency and upkeep of critical manufacturing equipment through effective troubleshooting techniques.
  • Exchanges ideas with other team members and participates in process improvements and changes.
  • Takes responsibility for project tasks and drives to meet deadlines.
  • Completes basic process engineering assessments and uses data to appropriately disposition product.
  • Provides process support on assigned Root Cause Analysis (RCA), Corrective Action Preventive Action (CAPA), implementing robust solutions to address root cause.
  • Generates, reviews, and approves engineering, manufacturing, and quality procedures necessary to support production operation, equipment validation/revalidation, and product launch.
  • Ensures adherence to Current Good Manufacturing Practices (cGMP).
  • Implements basic level changes to reduce process waste and variation and improve yields and product performance.
  • Reviews capital equipment fabrication activities to ensure manufacturing, installation, and operational testing conform to industry standards, and user requirements.
  • Generates capital requests to support new processes and capital equipment purchase.
  • Participates in equipment and process validations activities, including protocol and report writing, review and execution.
  • Initiate, reviews/approves change requests in Change Management system.
  • Develops implementation solutions to support operational needs.

 

Who You Are

 

Minimum Qualifications:

 

  • Bachelor degree in Mechanical Engineering, Chemical Engineering or other engineering discipline.

 

OR

 

  • High school diploma or GED.
  • 8+ years of experience in an FDA regulated medical device manufacturing facility, pharmaceutical facility or other regulated industry supporting automated or manual assembly processes.

 

Preferred Qualifications:

 

  • Master’s degree in Chemical Engineering.
  • Electro-Mechanical, instrument and pneumatic knowledge along with 2+ years of experience applying this knowledge to process/equipment troubleshooting.
  • Experience analyzing data sets, applying statistical analysis principles, and clearly summarizing conclusions/results.
  • Familiarity with EH&S, ISO, cGMP, and other regulatory requirements in a manufacturing environment.
  • Experience reading and understanding basic mechanical and electrical drawings and P&ID’s.
  • Experience with Microsoft products, Minitab, and CAD software packages.
  • Understand safe work practices and experience in lockout, tag out, electrical safety, etc.
  • Lean/Six Sigma experience, with green or black belt.

 

 


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!

 

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html

 

Job Requisition ID:  280332
Location:  Jaffrey
Career Level:  B - Recent University Graduate(<1 year of experien
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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Nearest Major Market: Bellows Falls
Nearest Secondary Market: Keene

Job Segment: Six Sigma Black Belt, Six Sigma, Lean Six Sigma, Medical Device, Testing, Management, Healthcare, Technology

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