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 Quality Assurance Supervisor at the Lenexa, KS site will supervise QA personnel to ensure raw material and finished product is released according to approved procedures. Job duties include:

• Supervise QA personnel to maintain Quality Systems.
• Coordinate and oversee the selection, training, development, motivation, and evaluation of employees.
• Interact with department personnel and provide daily supervision.
• Schedule the coordination of department personnel and provide problem solving and trouble-shooting assistance and support to department personnel.
• Supervise all aspects of batch record review and release for raw and final products and/or supervise all aspects of maintaining Quality systems.
• Investigate and resolve non-conformance and final release of products according to established lead times.
•  Provide assistance with investigations to ensure closure within established time frames and to ensure effective corrective actions have been implemented.
• Demonstrate leadership in developing and implementing quality system initiatives in all areas of Operations
• Lead escort duties for customer audits.
• Ensure timely closure of customer and supplier audit observations.
• Lead process improvement efforts within the Quality Assurance Department
• Perform managerial duties in the absence of the manager
• Participate in design, development, and approval of new products through the R&D Design Control process
• Function as independent reviewer, responsible for providing input on Quality requirements and ensuring compliance to all internal procedures and ISO standard
• Take part in and contribute to a safe working environment by following corporate and departmental safety regulations.
• Perform other job-related duties as assigned.

Who you are

Minimum Qualifications:

• Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, Biology, or life science discipline.
• 5 years of quality experience in a cGMP environment

Preferred Qualifications:

• Attention to detail, problem solving and organizational skills
• 2 years of supervisory experience
• Demonstrated leadership skills
• Strong interpersonal and communication skills.
• Ability to work with mathematical concepts and investigational techniques.
• Working knowledge of computer programs such as Microsoft Office Suite, SAP or BPCS
• Knowledge of cGMP and 21 CFR

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