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Quality Assurance Operations 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:

The Quality Assurance Operations supervisor is a driver of a mature quality culture, particularly through the implementation of quality assurance within operations. Quality assurance operations (QA Ops) function is present or easily accessible to operations in a Manufacturing facility to support data integrity, root cause analysis, data and batch review, document control and auditing.

 

  • Supervise employees to accomplish all departmental goals and objectives in safe manner and in compliance with all various state, federal and company regulations (OSHA, EPA, FDA, NRC, etc.)
  • Identify, evaluate, and implement process improvements
  • Lead team through day-to-day site operations and challenges, including prioritization and defect resolution
  • Pro-actively review Operating Procedures, update test specifications, modify as needed in accordance with change management procedures
  • Coach and facilitate systematic cause and effect problem solving to implement robust solutions for customer complaints and internal defects, including CAPA management. Report incidents, assist in investigating causes and follow up with appropriate actions
  • Manage quality trends and metrics to drive systematic process improvements and minimize the cost of poor quality.
  • Perform tasks as required for Quality Management System (QMS), including compliance with 21 CFR 210 and 211, Q7 and ISO 13485
  • Select, train, develop, motivate, and evaluate employees in a timely manner consistent with company policies. Lead and motivate through positive reinforcement, encouragement, example, and communication of company values
  • Develop employees to maximize performance. Communicate with employees, other departments, and management in a timely fashion. Quickly resolve personnel conflicts and problems as they arise

 

Who You Are

Minimum Qualifications:

  • Bachelor’s degree in any Life Science discipline.
  • 4+ years quality assurance in a cGMP environment.

OR

  • Associate’s degree in any Life Science discipline.
  • 4+ years of supervisor experience.
  • 4+ years quality assurance in a cGMP environment.

 

Preferred Qualifications:

  • Detailed knowledge of data integrity, data review, root cause analysis and auditing
  • Highly developed interpersonal, written and verbal skills with attention to detail. 
  • Strong team player – ability to collaborate across all departments within the organization to deliver on quality and regulatory commitments
  • Ability to work autonomously, effectively manage time, and deliver results on time
  • Prior supervisory or Lean Six Sigma experience
  • Familiar with cGMP, ISO, FDA Regulations
  • Strong communication, personal, and leadership skills
  • Planning, organizational and team building skills

 

Pay Range for this position: $82,900-$124,300.

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

 

RSREMD

 

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!

Job Requisition ID:  300436
Location:  Madison
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

Notice on Fraudulent Job Offers
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Job Segment: QA, Quality Assurance, Lean Six Sigma, Six Sigma, Document Control, Technology, Quality, Management, Administrative

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