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: The Buffer Manufacturing Team Lead at our Cherokee site will play a key role within our GMP Operations Systems & Support team (OSS). The Buffer Manufacturing Team Lead is responsible for overseeing and guiding Manufacturing Scientists and Technicians in the preparation and manufacturing of buffers and solutions. This role requires a proactive approach to identifying and resolving issues while fostering a positive and collaborative work environment. Job Duties Include: <ul style="margin-top:0.0in;margin-bottom:0.0in"> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">2nd shift hours: Monday – Friday, 2:00pm – 10:30pm</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Lead the buffer formulation team in the execution of cGMP buffer manufacturing.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. </li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Safely perform operations to meet quality expectations.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Maintain required training to perform tasks/assignments.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Perform routine processes and unit operations. </li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Clean equipment and working areas during and after operations.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Support facility functions (e.g., maintain equipment, prepare reagents, restock supplies, waste disposal).</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Revise and approve procedures, batch records, and other documentation to ensure compliance with cGMP guidelines.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Communicate the status of operations and convey concerns to the supervisor.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Provide complete and accurate records consistent with quality guidelines.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Ensure all applicable logbooks are completed as required by current procedures.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Work cross-functionally with Project Management, Technical Operations, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Help with MMF review</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Participate as needed in quality audits and customer interactions.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Improve processes by applying scientific knowledge, experience, and principles, in compliance with change control.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Take action to resolve unsafe conditions.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Train team members and act as technical consultants.</li> </ul> Physical Attributes: <ul style="margin-top:0.0in;margin-bottom:0.0in"> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Lift up to 50 pounds</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Personal protective equipment such as a respirator or chemical protective clothing for extended periods. </li> </ul> Who You Are Minimum Qualifications: <ul style="margin-top:0.0in;margin-bottom:0.0in"> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other scientific discipline</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">2+ years of experience in GMP manufacturing or operations, in a pharmaceutical or biotechnology environment.</li> </ul> OR <ul style="margin-top:0.0in;margin-bottom:0.0in"> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">High School Diploma or GED</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">4+ years’ experience of experience in GMP manufacturing, in a pharmaceutical or biotechnology environment.</li> </ul> Preferred Qualifications: <ul style="margin-top:0.0in;margin-bottom:0.0in"> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Excellent problem-solving abilities and a proactive approach to identifying and resolving issues, both process and mechanical.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Knowledge of process techniques, unit operations, and safe chemical handling methods.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Familiarity with regulatory requirements and industry best practices related to GMP manufacturing, including ICH regulatory and Quality standards.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Proficient in SAP, Microsoft Office and other software applications.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Strong leadership and interpersonal skills, with the ability to motivate and guide a diverse team.</li> <li style="margin:0.0in 0.0in 0.0in 24.0px;line-height:115%;font-size:12.0pt;font-family:verdana, geneva, sans-serif">Knowledge of Lean Manufacturing principles and continuous improvement methodologies (OpEx).</li> </ul> RSREMD <a name="_Hlk209520045"></a><a name="_Hlk208477024"></a>Pay Range for this position: $24.00 - $44.00. 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 <a href="https://careers.emdgroup.com/us/en/benefits" target="_blank" rel="noopener">here</a>. 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!

Buffer Manufacturing Team Lead - 2nd Shift (St. Louis, Missouri, US, 63118-3306) @ SUSONITY

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