Quality Supervisor

 

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: 

As the Quality Supervisor – Document Controls & Archives in Rockville, you will be a working supervisor with primary functional and administrative responsibility for a team who performs a range of tasks.   This encompasses report scanning and archival of regulated GxP (e.g., GLP, GMP) studies and management of the Document Control process including management of templates and issuing controlled documents.  

 

Essential Job Functions: 

• Supervise staff and organize employees’ schedules. 

• Assign and monitor work distribution and performance across the team using appropriate tools. 

• Provide and/or ensure appropriate training, coaching and professional development for personnel.  

• Provide feedback, complete performance reviews, document performance problems and take appropriate action.  

• Monitor expenses and resources within department budget. 

• Provide support for regulatory inspections. 

• Participate on local quality improvement project teams. 

 

Who You Are

 

Minimum Qualifications:

• Bachelor’s Degree in any discipline. 

• 4+ years of experience in Quality Assurance or related field within a GxP environment.  

• 1+ years supervisory or team lead experience.

 

Preferred Qualifications:

• Experience with archives or document control in a quality environment
• Bachelor’s degree in a Science or Technical field.
• Acts ethically and ensures quality of own work and that of the QA team. 

• Collaborates with various teams to identify and implement improvements. 

• Applies technology to drive digitalization, improve quality and increase customer value. 

• Works with agility and strong verbal and written communication.

• Expert knowledge and application of FDA and EU regulations (cGMP, GLP, Archiving). 
• Excellent communication, facilitation, and conflict resolution skills. 

 

Pay Range for this position - $74,600k - $111,900k

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!