Work Your Magic with us! Start your next chapter and join EMD Electronics.

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.

Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers.

Your Role:

At MilliporeSigma, the Senior Associate Quality Scientist will perform Quality Control activities in support of raw materials of cGMP products, including routine testing (in-house and compendial) and peer review of data. In addition, testing of Environmental Monitoring (EM) and cleaning verification samples will be performed.

• Perform routine testing and peer review of raw material samples through adherence to applicable GMP requirements.
• Utilize written procedures to perform routine and non-routine product testing.
• Revise procedures through use of the Document Management System (DMS) following Good Documentation Practices (GDP).
• Work in accordance with current GMPs and demonstrate proper laboratory safety and housekeeping practices.
• Participate in method development and validation activities to support product testing.
• Contribute to support function of the laboratory through participation in laboratory audits to maintain compliance.
• Participate in deviation investigations.
• Train analysts on basic analytical techniques.
• Contribute and lead process improvement projects.
• Wear personal protective equipment including but not limited to: safety glasses, gloves and respirator.

Who You Are:

Minimum Qualifications:

• Bachelor’s Degree in the Life or Physical Sciences field.
• 2 + years of GMP laboratory experience.

Preferred Qualifications:

• General laboratory techniques (theory and practice).
• Experience with various laboratory equipment.
• Working Knowledge of Good Manufacturing Practices for pharmaceutical manufacturing (21 CFR 210 & 211 and/or ICH Q7A).

• Knowledge of Microsoft Word, Excel and Access.
• Strong time management, verbal and written communication skills.

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