CDMO Project Manager

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 We are looking for a successful, true Project Manager for our Cherokee CDMO (Custom Development Manufacturing Organization) site in St. Louis. Responsibilities Own and execute complex, fast‑paced projects (expansions, new products, operational excellence) from scope through to delivery. Partner with internal and external stakeholders, leveraging strong interpersonal skills to influence teams without direct authority. Proactively identify project risks, collaborate with key stakeholders to resolve critical issues, and minimize organizational impact. Facilitate productive meetings for diverse audiences and provide regular, proactive progress updates to clients and leadership. Create and maintain essential project artifacts, including charters, schedules, budgets, change controls, and risk logs. Mentor and coach project management personnel across the organization, capturing lessons learned for continuous improvement. Minimum Qualifications Bachelor’s degree in engineering or life science discipline and 5+ years of Project Management experience. High School Diploma or GED and 10+ years of Project Management experience. Preferred Qualifications PMP Certification and proficiency with Smartsheet or equivalent project management tools. Proven project management experience within a highly regulated GMP, Biotech, or Pharma manufacturing environment. Strong familiarity with FDA, EMA, and other global regulatory standards. Independent self‑starter with a track record of driving cross‑functional results in biopharmaceutical operations. Exceptional attention to detail with experience in meticulous document review and strict adherence to procedures. Strong analytical and problem‑solving skills with the ability to identify risks and communicate them clearly. Excellent oral and written communication skills across all levels of internal and external stakeholder. Salary range for this position: $89,000 - $133,600 annually. 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. 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! #J-18808-Ljbffr MilliporeSigma