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:
- Provide key engineering support and project coordination for all phases of plant operations, including interfacing with internal and external clients for product technology transfers and manufacturing.
- Offer technical support for processes and product investigations, and continuously improve manufacturing processes, including technical transfer and scale-up of new product introductions.
- Become a Subject Matter Expert (SME) for multiple product lines (preclinical through commercial) by applying extensive process knowledge and experience.
- Coordinate and execute technology transfer projects for new clinical and commercial products and contract manufacturing opportunities, serving as the main technical interface with external/internal clients.
- Manage project deliverables by coordinating with multiple internal and external departments and executing small to medium-scale technical projects up to $250K in value.
- Perform process and equipment design engineering, including project estimating, budgeting, developing capital appropriation requests, documentation updates, scheduling, and overall project coordination.
- Provide project and process engineering support for technical projects, including equipment specification and procurement, process and drawing development, and protocol development/execution.
- Develop and modify engineering drawings, SOPs, control loops/strategies, and perform calculations (hydraulic, heat transfer, material balances), while also leading and executing validation protocols (IQ, OQ, PQ) for various systems.
Physical Attributes:
- Climb stairs and ladders.
Who You Are:
Minimum Qualifications:
- Bachelors Degree in Biology, Microbiology, Biochemical Engineering, Chemical Engineering, or other Life Science or Engineering discipline and 2+ years of work experience with US and European GMP requirements, FDA guidelines, and industry validation expectations.
OR
- Masters Degree in Biology, Microbiology, Biochemical Engineering, Chemical Engineering, or other Life Science or Engineering discipline and 1+ years of work experience with US and European GMP requirements, FDA guidelines, and industry validation expectations.
Preferred Qualifications:
- Experience with aseptic manufacturing processes and packaging equipment, unit operations, process control systems, computer systems, equipment cleaning, sterility assurance, process hazards and safety.
- Experience with Microsoft Office Suite.
- Experience with AutoCAD, Minitab, or JMP.
- Experience with Root Cause Analysis methodology, FMEA or another program.
RSREMD
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!