What are the responsibilities and job description for the QA Senior Associate position at MilliporeSigma?
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 (QA) Senior Associate position at MilliporeSigma Verona, WI is a critical part of the Quality Assurance Operations (QA Ops) team and will perform data and batch review and release and document control functions. The QA Sr. Associate is responsible for guidance and coaching during operations, as well as auditing manufacturing, quality control, and materials management areas, providing immediate review with constructive feedback. Additional responsibilities include the following:
Minimum Qualifications:
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.
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!
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 (QA) Senior Associate position at MilliporeSigma Verona, WI is a critical part of the Quality Assurance Operations (QA Ops) team and will perform data and batch review and release and document control functions. The QA Sr. Associate is responsible for guidance and coaching during operations, as well as auditing manufacturing, quality control, and materials management areas, providing immediate review with constructive feedback. Additional responsibilities include the following:
- Uphold ethics and quality in own work and that of others.
- Ensure on-time deliverables by collaborating with cross-functional teams.
- Review batch records and related cGMP documentation; generate certificates of analysis and other needed documentation to support batch release.
- Ensure GMP documentation are completed timely, attributable, legible, traceable, complete, and compliant for release.
- Prepare production execution documents (batch records, logs, packaging/shipping) for cGMP operations.
- Own Right-First-Time metrics and QA Ops KPIs; conduct self-inspections and support continuous improvement projects.
Minimum Qualifications:
- Bachelor’s degree in Biology, Chemistry, Chemical Engineering, Physics, or other Life Science discipline
- High School Diploma or GED
- 3 years of GMP experience
- Basic knowledge of FDA regulations (21 CFR Parts 11, 210, 211 etc.)
- Experience in Quality Assurance field within a GMP environment
- Familiarity with International regulations
- Strong oral and written communication and interpersonal skills
- Open-minded, flexible, and capacity to work with agility
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.
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!
Salary : $26 - $46