Sr. Quality Assurance Associate
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 Sr. Quality Assurance Associate at MilliporeSigma in Sheboygan Falls, WI, will work as a TrackWise Change Coordinator supporting quality systems, and ensuring their alignment with business goals, premier customer expectations and requirements, as well as global business unit best practices. The Associate will establish strong collaborative relationships with all departments within the organization and will deliver on quality and regulatory commitments, working autonomously to effectively manage delivery of results within targeted deadlines.
- Change Management Quality system development and maintenance
- Genesis and TrackWise Change Coordinator
- Reporting for internal and external customers
- Document Control
- Employee Training
- Weekly schedule, days/hours: Monday – Friday, 7:00 AM – 3:30 PM. This is a hybrid position; however, the Associate must be able to work on site as the job requires (typically 2-3 days per week) and possibly 40 hours per week as projects necessitate
Physical Attributes:
- View computer monitors for extended periods of time
- Sitting, standing, and walking for extended periods of time
- Use of phones, computers, computer monitors and office/laboratory equipment
Who You Are
Minimum Qualifications:
- Bachelor's Degree in Chemistry, Biology, Healthcare, or other Life Science discipline
OR
- High School Diploma or GED AND 2+ years of experience in an industrial, manufacturing or production environment
Preferred Qualifications:
- Life science, chemical, electronics, or healthcare industry knowledge
- Excellent communication skills both verbal and written
- Understanding of Quality System Regulations, ISO Quality Systems, and other FDA Regulations
- Strong computer skills, including proficiency in MS Word, MS Excel, MS Access, MS PowerPoint, Google, and ERP systems
- Excellent problem-solving skills/abilities with the ability to implement solutions to problems or situational changes
- Good time management skills
- Ability to increase efficiencies in the continuous improvement of the quality management system
- Good team player
- Enthusiastic and flexible
- Agent for change and improvement
- Ability to work independently and in a fast-paced, team environment
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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QA, Quality Assurance, Document Control, Developer, Quality, Technology, Administrative