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

 

You will join a team of supervisors that are accountable for management of a 24/7, large scale manufacturing area; oversee safe operations within production activities associated with a mix of protein purification, nucleotide manufacturing and biosynthetic processes.

Specific job duties include: 
  

Your responsibility will include 3rd shift supervision and development of a team (5-8 employees) and be accountable to meet business performance metrics/ KPIs. You will manage and prioritize shift scheduling so products are released in a timely manner; track and manage a department budget and capital expenditure budget.In this role you will develop and implement programs to establish and maintain quality systems, and quality standards of existing products and services, as well as developing programs to focus employees on quality improvements, develop policies, procedures and methods to check and improve product, material, components, processes and/or operational quality.Interface with internal customers on regular basis to communicate project status, resolve issues; implement methods, techniques and evaluation criteria for products and processes. You will perform other duties as required by your management.

  

Who You Are 

 

Minimum Qualifications: 

 

Bachelor's Degree in Biochemistry, Biology, or other Life Science Discipline.

Preferred Qualifications: 

 

1+ years of experience as a supervisor, or lead in a regulated environment.Experience working in a highly matrixed organization.Strong written and verbal communication skills, with the ability to translate complex issues into straightforward and succinct explanation.Strong skills in root cause analysis and problem resolution. Strong computer skills, including word processing.Strong understanding of PSM regulations.Background of mechanical troubleshooting.Leadership and team building skills.Knowledge of pharma/biotech bulk and finished product manufacturing and testing requirements.

RSREMD

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