Overview
On Site
Full Time
Skills
Value Engineering
Health Care
Electronics
Testing
FOCUS
Process Control
Assembly
Material Handling
Process Improvement
Process Engineering
Evaluation
Root Cause Analysis
Corrective And Preventive Action
Regulatory Compliance
Technical Writing
Documentation
Management
System Integration Testing
Biology
Chemical Engineering
Life Sciences
Medical Devices
Pharmaceutics
ISO 9000
Good Manufacturing Practice
Manufacturing
Mechanical Engineering
Electrical Engineering
IDS
Microsoft Office
Minitab
Software Packaging
Lean Six Sigma
Innovation
Science
MAGIC
Job Details
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.
Your Role:
In this role you are 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.
Duties include but are not limited to:
Expert troubleshooter for manufacturing equipment and processes, adept at diagnosing and resolving intermediate-level issues to maintain efficiency.
Proven leader in driving process improvements, leading cross-functional teams, and building consensus for strategic changes and capital equipment initiatives.
Skilled in process engineering assessments, data-driven product disposition, and independent evaluation of moderate to intermediate-level tasks.
Proficient in Root Cause Analysis (RCA) and CAPA, implementing robust solutions, and ensuring compliance with cGMP through strong technical writing and documentation.
Experienced in capital equipment management, from justification and purchase to fabrication, installation, and validation activities.
Physical Attributes:
Who You Are:
Minimum Qualifications:
OR
Preferred Qualifications:
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!
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.
Your Role:
In this role you are 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.
Duties include but are not limited to:
Expert troubleshooter for manufacturing equipment and processes, adept at diagnosing and resolving intermediate-level issues to maintain efficiency.
Proven leader in driving process improvements, leading cross-functional teams, and building consensus for strategic changes and capital equipment initiatives.
Skilled in process engineering assessments, data-driven product disposition, and independent evaluation of moderate to intermediate-level tasks.
Proficient in Root Cause Analysis (RCA) and CAPA, implementing robust solutions, and ensuring compliance with cGMP through strong technical writing and documentation.
Experienced in capital equipment management, from justification and purchase to fabrication, installation, and validation activities.
Physical Attributes:
- Exposure to chemical reagents.
- Sit, stand, and walk for extended periods of time.
- Lifting and carrying up to 50 pounds.
Who You Are:
Minimum Qualifications:
- Bachelors Degree in Biology, Chemical Engineering, or other Life Science or Engineering discipline.
OR
- High School Diploma or GED and 8+ years of experience in an FDA regulated medical device manufacturing facility or pharmaceutical facility.
Preferred Qualifications:
- Masters Degree in Engineering.
- 3+ years of electro-mechanical experience.
- Experience with EH&S, ISO, cGMP, and other regulatory requirements in a manufacturing environment.
- Experience reading intermediate level mechanical and electrical drawings and P&IDs.
- Experience with Microsoft products, Minitab, and CAD software packages.
- Lean Six Sigma green or black belt.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!
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