Manufacturing Supervisor - PM 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 cGMP Manufacturing Supervisor at the St. Louis Cherokee site will lead a dedicated team in the production of Bulk Pharmaceutical Chemicals and Active Pharmaceutical Ingredients that enhance healthcare under FDA regulations. The role will involve motivating team members to excel, supporting their professional development, and collaborating effectively with Customers, R&D, and QA/QC to meet departmental and company goals. The job duties include:

• Shift: Rotational 12 – hour Shift: Shift hours: 6:00pm – 6:30am, some holidays and every other weekend 
• Supervise employees to accomplish all departmental goals and objectives in a safe manner and in compliance with all applicable federal, state and company regulations (OSHA, EPA, NRC, ATF, FDA, etc.)
• Ensure tasks are done in accordance with approved OPs, MMFs and other cGMP protocols and that processes proceed correctly
• Provide strong avenue of communication for employees and ensure information is passed on to subordinates in a timely fashion through weekly meetings and shift pass downs
• Communicate the group’s status, data and feedback to management
• Direct Group's efforts toward Process improvement and company goals
• Approve and sign for production any Master Manufacturing Formulas, Operating Procedures, batch records and other documentation to ensure compliance with FDA and cGMP guidelines
• Plan for short-term and long-term response to customer needs and company goals
• Contribute to the support of customer relations. Interact with the customers and represent the company during audits. 

Who You Are

Minimum Qualifications:

• Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, Biology or other life science
• 3+ years technical production or R&D experience in a Manufacturing Facility
• 3+ years of lead, manager, or supervisor experience within a manufacturing, lab, quality control or operations setting

Preferred Qualifications

• Experience with cGMP Manufacturing
• Basic chemistry and science principles; This facility specializes in Organic Synthesis
• Knowledge of various relevant processing techniques and equipment
• Ability to manage, motivate and develop employees
• Interpersonal skills, conflict resolution, motivation, leadership
• Communications skills including writing and oral, ability to communicate with various disciplines and levels both one-on-one and group communication
• Knowledge of Process Improvement methodology

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