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:

This position is located in the Ewing location. The Quality Assurance Specialist provides compliance oversight across the MilliporeSigma Quality Management System (QMS) in collaboration with site personnel. In this role you are responsible for the implementation and maintenance of Quality Systems and processes to ensure internal and external compliance and the promotion of quality practices that meet or exceed required guidelines and regulatory requirements.

Responsibilities include but are not limited to:

• Improve quality systems in ISO and non- GMP production environments.
• Drive quality improvement in multiple departments.
• Complete a high volume of work to meet department goals.
• Communicate the status of operations and bring critical deviations to the attention of your manager.
• Communicate with coworkers and interact with other departments on a regular basis.
• Complete and have accurate work consistently with quality guidelines.
• Assist in maintaining department KPIs through on time CAPAs, Deviations, Complaints and Change Controls.
• Assist in compliance with Life Science and site quality policies and procedures.
• Represent the site during customer and regulatory audits.
• Perform internal audits.
• Assist in the investigation of customer complaints.
• Contribute to Root Cause Investigations & Effectiveness Checks of Nonconforming Incidents.
• Conduct Quality System Training.
• Documentation control activities include management of the electronic documentation management system, and writing, reviewing, or approving Operation Procedures, Specifications, Master Manufacturing & Packaging Procedures and other controlled documents.
• Improve processes through application of scientific knowledge, experience, and principles in compliance with change control procedures.
• Identify opportunities for process improvement.
• Interpret analytical evaluations of products and intermediates.

Who You Are:

Minimum Qualifications:

• Bachelors Degree in Biology, Chemistry, or other Life Science discipline and 4+ years of Quality Assurance work experience.
• Masters Degree in Biology, Chemistry, or other Life Science discipline and 2+ years of Quality Assurance work experience.

Preferred Qualifications:

• Experience maintaining lab equipment, preparing reagents, restocking lab supplies, and proper waste disposal.
• Experience with Quality Control procedures such as ELISA and other chemistry methods.

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