Principal Project Engineer

Millipore Corporation; Lenexa (KS); On-site; USD 107,000 - 173,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement contributions

Perquisites

Job summary

MilliporeSigma in Lenexa, KS, seeks a Principal Project Engineer to lead cell culture media manufacturing projects, focusing on design, qualification, and optimization of equipment and facilities for safe, compliant production.

You will manage capital and process-improvement initiatives, coordinate with engineering, manufacturing, quality and EHS, and mentor teams to uphold data integrity, change control, and continuous improvement.

Qualifications

• Bachelor's degree in Chemical, Biochemical, Mechanical, or Biomedical Engineering (or a closely related field).
• Master's degree preferred.
• 5+ years of professional engineering experience.
• Experience managing projects over $1M.

Responsibilities

• Lead projects related to design, qualification, and optimization of cell culture media manufacturing equipment and facilities.
• Develop project scope and ensure seamless implementation of efficient technical solutions.
• Collaborate with process engineering, manufacturing, quality, EHS, and maintenance for robust design, commissioning, qualification, and readiness.
• Drive project timing, budget, risk management, and present status reports to leadership.
• Mentor engineers and cross-functional teams to foster safety, quality, and continuous improvement.

Skills

Project management

Leadership

Risk assessment

Technical writing

Communication

Education

Bachelor's degree in Chemical/Biochemical/Mechanical/Biomedical Engineering

Master's degree preferred

Tools

IQ/OQ/PQ validation

Automation concepts

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:

As a Principal Project Engineer at the Lenexa, KS site, you will lead key projects related to the design, qualification, and optimization of the cell culture media manufacturing equipment and facilities to ensure safe, compliant, and scalable production of high-quality media for biopharmaceutical applications.

This includes technical project management for both capital projects and process improvements. You will develop project scope and ensure seamless implementation of the most efficient, viable technical solution in alignment with internal standards. You will collaborate with process engineering, manufacturing, quality, EHS, and maintenance to ensure robust design, commissioning, qualification, and operational readiness. Additionally, you will drive project timing, budget, and risk management, and prepare and present status reports to leadership and stakeholders. You will ensure adherence to data integrity and change-control practices, owning the engineering change process, and you will mentor engineers and cross-functional teams to foster a culture of safety, quality, and continuous improvement. You will identify and implement cost‑saving opportunities, technology upgrades, and energy/water efficiency improvements, and ensure facilities and equipment meet regulatory and MilliporeSigma corporate standards for cell culture media manufacturing operations.

Who You Are

Minimum Qualifications:

• Education: Bachelor's degree in Chemical, Biochemical, Mechanical, or Biomedical Engineering (or a closely related field)
• Master's degree preferred5+ years of professional engineering experience
• Experience managing projects over $1M

Preferred Qualifications:

Technical competencies:

• Experience with validation strategies (IQ/OQ/PQ) and commissioning/ qualification activities
• Familiarity with automation concepts, sensors, control systems, data integrity, and change control

Skills:

• Proven project management and leadership capabilities; ability to influence across functions; excellent problem-solving, risk assessment, and decision‑making skills; strong communication and technical writing abilities
• Experience in medical, biotechnology, or Bio‑pharmaceutical manufacturing environment is highly preferred
• PMP certification preferred

Pay Range for this position: $106,500 - $172,900

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. For more information click here.

Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.

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!