Quality Assurance Specialist

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 Specialist will facilitate and support the development, maintenance, and improvement of quality systems, to ensure their alignment with business goals, customer expectations, and requirements for global business unit best practices. This position will have a strong focus in Supplier Quality Management and general Quality Management System requirements and improvements. Responsibilities to include the following:

• Quality system development and maintenance activities
• Support supplier quality management activities and programs
• Lead and facilitate supplier development activities including audits
• Lead, facilitate and support various quality system initiatives

Physical Attributes:

• View computer monitors for long periods of time
• Regular use of phones, computers, computer monitors and office equipment

Who you are:

Minimum Qualifications:

• Bachelor’s degree in science, engineering, or business/mathematics including course work in chemistry or other science discipline

     OR

• High School Diploma and 3+ years of work experience in a quality role or 5+ years in a production, or project management role

Preferred Qualifications:

• 3+ years of knowledge and experience in Quality Management Systems, ISO Quality Standards, and other regulatory standards as appropriate. (FDA, VDA, DOT, IATA, DEA, etc.)
• 1+ year of knowledge and experience in 21CFR117
• Hosting and performing internal and external audits
• Understanding of data analysis, presentation, and experimental design
• Ability to work independently and in a fast-paced, team environment
• Ability to simultaneously manage multiple tasks and priorities
• Understanding of current processing requirements for food, drug, industrial, and biologic types of products
• Demonstrated leadership and strong problem-solving skills
• Excellent oral and written communication skills
• Strong computer skills
• Life science, Chemical, Food Industry, or Healthcare industry knowledge
• Knowledge of SAP, TrackWise, Document Control Systems, and Microsoft Office
• Experience in preparing and reviewing documentation to ensure compliance with company or customer quality requirements
• Ability to increase efficiencies in the continuous improvement of the quality management system

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