Process Engineer
Listed on 2026-07-14
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Engineering
Process Engineer, Quality Engineering, Manufacturing Engineer -
Manufacturing / Production
Quality Engineering, Manufacturing Engineer
Work Your Magic with us! Start your next chapter and join Millipore Sigma. 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 RoleThe Process Engineer is responsible for supporting the manufacturing and testing of membranes used in high‑purity filtration products while maintaining a strong focus on safety, quality, process control, electro‑mechanical assembly, and material handling. The engineer will establish and optimize operating specifications, implement process improvements, and troubleshoot manufacturing issues to improve efficiency, product quality, and overall performance. The role includes monitoring machinery, automated equipment, and manufacturing processes;
investigating complex production challenges; identifying root causes; and implementing corrective actions to ensure reliable operations. Working closely with Manufacturing, Quality, Maintenance, and other cross‑functional teams, the engineer will help drive process stability, evaluate product quality, reduce waste, improve yields and productivity, and support continuous improvement initiatives within a regulated manufacturing environment.
- Responsible for maintaining efficiency and upkeep of critical manufacturing equipment through effective troubleshooting techniques.
- Exchanges ideas with other team members and participates/ leads technical discussions to realize process improvements and changes.
- Provides basic leads process support on assigned Root Cause Analysis (RCA), Corrective Action Preventive Action (CAPA), implementing robust solutions to address root cause of issues.
- Responsible for generating, reviewing, and approving engineering, manufacturing, and quality procedures necessary to support production operation, equipment validation/revalidation, and product launch.
- Ensures adherence to Current Good Manufacturing Practices (cGMP).
- Leads and implements basic level changes to reduce process waste and variation, and improve yields and product performance initiatives.
- Generates capital requests to support new processes and capital equipment purchase.
- Works collaboratively with cross‑functional teams, takes ownership of project tasks and deadlines, and conducts basic process engineering assessments using data to make informed product disposition decisions.
- Reviews capital equipment fabrication activities to ensure manufacturing, installation, and operational testing conform to industry standards and user requirements.
This is a weekend position working 3 × 12‑hour shifts on Saturday, Sunday, and one weekday of choice.
Minimum Qualifications- Bachelor’s degree in chemical engineering, electrical engineering, mechanical engineering, business management, computer science, or other life science discipline.
OR
- High School diploma and 8+ years of experience in an FDA‑regulated medical device manufacturing facility, pharmaceutical facility, or other regulated industry supporting automated or manual assembly processes.
- Master of Science Degree in Electrical, Mechanical, Chemical, or Industrial Engineering.
- Basic electro‑mechanical, instrument, and pneumatic knowledge along with 2+ years of experience applying this knowledge to process/equipment design and/or troubleshooting.
- Proven ability to analyze data sets, apply statistical analysis principles, and clearly summarize conclusions/results.
- Familiarity with EH&S, ISO, cGMP, and other regulatory requirements in a manufacturing environment.
- Read and understand basic mechanical and electrical drawings and P&’s.
- Experience with Microsoft products, Minitab, and CAD software packages.
- Demonstrates a strong foundation in safe…
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