Process Engineer 2

 

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:

In this role you will be responsible for executing business unit driven process development programs using practical application of fundamental engineering principles in a cGMP setting associated with sterile injectable products. Responsible for providing key engineering/technical support and project coordination.  Responsible for interfacing with internal and external clients in support of product technology transfer, manufacture and investigations. Tech Support efforts primarily focus on process engineering, scale-up and continued support for complex formulations such as PEGylated formulations as well as Liposomal and Lipid Nanoparticles (LNP) based formulations. Importantly, this specific role will help facilitate the transfer and introduction of new chemical processes from the development lab or directly from the client through to full-scale manufacture as well as technical support for the improvement and optimization of chemical processes. 

Responsibilities include but are not limited to:

• Provide technical support for the manufacturing processes, including process investigations, continuous process improvements, technology transfer and scale up of new product introductions.  
• Leverage process knowledge/experiences to become a subject matter expert (SME) for multiple product lines (preclinical through commercial).
• Coordinate and execute small to medium scale and/or complex technical projects. Associated functions include process and equipment design engineering, project estimating and budgeting, developing capital appropriation requests, documentation updates, scheduling and overall project coordination and oversight. Project staffing will be comprised of personnel from various departments on-site, as well as contract personnel.
• Coordinate and execute tech transfer projects in support of new clinical and commercial products and contract manufacturing opportunities. In addition to project management responsibilities described above, will be the main technical interface with external / internal clients and contractors in support of contract manufacturing opportunities.
• Provide project and process engineering support for technical projects. Associated tasks include equipment specification and procurement, process development, drawing development, protocol development and execution.  
• Interpret, modify and create engineering drawings, including Piping and Instrumentation Diagrams, Piping Drawings, Layouts, Isometrics, Building Mechanical, Instrumentation and Electrical Drawings.  
• Creation of Standard Operating Procedures (SOPs) for new equipment/processes, as well as update of existing SOPs.  
• Perform process and utility calculations as related to hydraulic design, heat transfer, material balances, etc. 
• Lead and provide technical support for process investigations.  

 

Physical Attributes:

• Regular use of stairs and ladders.
• Wear goggles, gloves, and various personal protective equipment.

 

Who You Are:

Minimum Qualifications:

• Bachelor’s Degree in Chemical Engineering, Biochemical Engineering, or other Engineering discipline.
• 2+ years of engineering experience within a pharmaceutical company.

 

Preferred Qualifications:

• Experience with US and European GMP requirements, FDA guidelines, and industry validation expectations.
• Strong critical thinking, multi-tasking, & technical skills.  
• Prior experience with Lipid Nanoparticles, Liposomes, PEGylated formulations, Lyophilization unit operations and/or other nanomedicinal parenteral products.
• Experience with spreadsheets, word processing, databases, and Microsoft Project.
• Experience with Root Cause Analysis methodology.
• Experience with Microsoft Visio, AutoCAD, or similar drawing program. 
• Experience with Minitab, Jump, or similar statistical software. 

 

Pay Range for this position: $75,900 - $120,800​

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. 

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!