Quality Systems Specialist Job at MilliporeSigma

MilliporeSigma Bellefonte, PA 16823

Work Your Magic with us!

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.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

The Quality Systems Specialist at MilliporeSigma in Bellefonte, PA will have the following job duties :


  • Support Quality Management System through audits, inspections of materials, processes, equipment, corrective actions, deviations, risk analysis, and implementation of quality measures
  • Aid in ensuring compliance to Quality Systems regulations including ISO 9001:2015 Standard and corporate requirements
  • Participate in audit program which includes internal, customer, supplier, and registrar audits
  • Support functional areas by conducting data and document review/approval as it pertains to the quality systems - ensure that processes and products consistently meet established quality standards
  • Support the QMS through review and approval of product/process investigations, deviations, OOS, and participation in root cause analysis, CAPA, documentation management, and change management
  • Management of quality metrics/KPIs and their review through trend analysis and interpretation
  • Other duties as assigned
Who You Are:

Minimum Qualifications:


  • Bachelor's Degree in Chemistry, Biology, Biochemistry, or other life science discipline
  • 1 + year of work experience in Quality Assurance
  • 1 + years of experience in ISO 9001:2015 environment
Preferred Qualifications:


  • Understanding and application of the ISO 9001 Quality Management System
  • Ability to work in manufacturing and chemical manufacturing environments
  • Ability to work with and around machinery
  • Experience with risk management tools
  • Ability to hear
  • Experience with CAPA and Root Cause Analysis
  • Strong communication, organizational, and interpersonal skills
  • Ability to work independently and in with a team
  • Strong computer skills including Microsoft Office

RSRMS

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



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