Project Engineer 2 at Millipore Corporation in Peterborough, New Hampshire

Job Description:

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:



This role will manage several product development projects concurrently for the site. In this role you will work across several cross functional areas, including Quality, Purchasing, Marketing, R&D, Operations, and Environmental Health and Safety to ensure a seamless transition of new products from R&D to manufacturing.


Responsibilities include but are not limited to:

• Serve as the bridge between R&D and manufacturing for new products.


• Aid in all validation strategies for new products and equipment.


• Evaluate any risks to manufacturing during development process before project is released to manufacturing.


• Procure necessary contractors, materials, and equipment to support projects.


• Coordinate schedules with stakeholders and manufacturing, manage the day-to-day project activity, and manage the knowledge transfer from end of project to manufacturing startup.

• Responsibility for the turnover package to site support teams including AutoCAD drawings, PM plans, spare parts, asset records, and knowledge transfer.

• Review and approve pertinent NPI documentation such as purchase specifications, validation protocols and reports, standard operating procedures, etc.


• Ensure compliance with good manufacturing practices and good documentation practices.


• Ensure team applies safe work practices.

Who You Are:




Minimum Qualifications:

• Bachelors Degree in Chemical Engineering, Biomedical Engineering, or other Engineering discipline.


• 4+ years of engineering experience within a manufacturing, pharmaceutical, research and development, or chemical production environment.


• 4+ years of experience in Microsoft Word, Excel, and PowerPoint.

Preferred Qualifications:

• 5+ years engineering experience within a pharmaceutical, chemical, or other production experience.


• Experience working with GMP and GDP.

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 Apply Now