Filling Process Engineer at Millipore Corporation in Indianapolis, Indiana

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:



Working in conjunction with the Manufacturing Manager, Sterile and Packaging Operations, this role


is responsible for technical ownership of manufacturing operations. This person will provide engineering support and project coordination primarily to aseptic fill/finish manufacturing processes. Additionally, this position will be responsible for process improvement initiatives, process investigations, change control, material evaluation as related to the areas of responsibility.


Responsibilities include but are not limited to:

• Technical owner of aseptic fill/finish processes.


• Primary owner of process investigations and process change controls related aseptic fill/finish.


• Responsible for integration of new isolated fill line with lyophilization capabilities as part of overall


• facility expansion project.


• Generate internal and external User Requirement Specification for new equipment.


• Act as the subject matter expert on aseptic fill/finish and the validated parameters of each.


• Solves complex problems; gains a new perspective using existing solutions.


• Creates and revises Standard Operating Procedures (SOPs) and Master Production Control Records


• (MPCRs) for new equipment and processes.


• Serves as manufacturing technical representative on new product teams.


• Initiates and conducts cost reduction studies to reduce material cost or effect changes that result in


• higher production rates, greater efficiency, less waste, and reduction in labor requirements.


• Provides guidance and training to Production Technicians on manufacturing operations and


• processes.


• Contributes to process improvements, evaluating and recommending efficient inspection and


• packaging procedures.

Who You Are:




Minimum Qualifications:

• Bachelors Degree in Biology, Chemistry, Chemical Engineering, or other Life Science or Engineering discipline.


• 3+ years of inspection and/or packaging work experience in a pharmaceutical environment.

Preferred Qualifications:

• 5+ years of experience in manufacturing, validation, quality assurance, or engineering.


• 5+ years of experience in a regulated GMP environment (food or pharma).


• Experience with US and European GMP requirements, and FDA guidelines.

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