Buffer Manufacturing Team Lead - Night Shift

 

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 - Night Shift 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. The GMP Packaging Lead will drive compliance with all applicable regulations and maintain a safe and efficient work environment.  Job duties include:

 

• Shift details This role will support 24/7 manufacturing operations and work 12-hour shifts from 6PM – 6:30 AM with 20% shift differential.
• Lead the buffer formulation team in the execution of cGMP buffer manufacturing.
• Evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department. 
• Safely perform operations to meet quality expectations.
• Maintain required training to perform tasks/assignments.
• Perform routine processes and unit operations. 
• Clean equipment and working areas during and after operations.
• Support facility functions (e.g., maintain equipment, prepare reagents, restock supplies, waste disposal).
• Assist with Buffer formulation Schedule and communication with ADC
• Revise and approve procedures, batch records, and other documentation to ensure compliance with cGMP guidelines.
• Communicate the status of operations and convey concerns to the supervisor.
• Provide complete and accurate records consistent with quality guidelines.
• Ensure all applicable logbooks are completed as required by current procedures.
• Work cross-functionally with Project Management, Technical Operations, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance.
• Help with MMF review
• Participate as needed in quality audits and customer interactions.
• Improve processes by applying scientific knowledge, experience, and principles, in compliance with change control.
• Take action to resolve unsafe conditions.
• Train team members and act as technical consultants.

 

Physical Attributes:

• Lift up to 35 lb.
• Personal protective equipment such as a respirator or chemical protective clothing for extended periods. 

 

Who you are:

 

Minimum Qualifications:

 

• Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other scientific discipline
• 2+ years of experience in GMP manufacturing or operations, in a pharmaceutical or biotechnology environment.

                                               OR

• High School Diploma or GED
• 4+ years’ experience of experience in GMP manufacturing, in a pharmaceutical or biotechnology environment.

 

 

Preferred Qualifications:

• Excellent problem-solving abilities and a proactive approach to identifying and resolving issues, both process and mechanical.
• Knowledge of process techniques, unit operations, and safe chemical handling methods.
• Familiarity with regulatory requirements and industry best practices related to GMP manufacturing, including ICH regulatory and Quality standards.
• Proficient in SAP, Microsoft Office and other software applications.
• Strong leadership and interpersonal skills, with the ability to motivate and guide a diverse team.
• Knowledge of Lean Manufacturing principles and continuous improvement methodologies (OpEx).

RSREMD

 

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 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!