Senior Quality Assurance Associate

JOB REQUIREMENTS: Duties and Responsibilties of Job: Work Your Magicwith us Start your next chapter and join MilliporeSigma. Ready toexplore, break barriers, and discover more? We know you've got bigplans - so do we Our colleagues across the globe love innovating withscience and technology to enrich people's lives with our solutions inHealthcare, Life Science, and Electronics. Together, we dream big andare passionate about caring for our rich mix of people, customers,patients, and planet. That's why we are always looking for curiousminds that see themselves imagining the unimaginable with us. This roledoes not offer sponsorship for work authorization. External applicantsmust be eligible to work in the US. Your Role: The Senior QualityAssurance Associate in Milwaukee, WI provides compliance oversightacross the MilliporeSigma Quality Management System (QMS) incollaboration with site personnel. As a Quality Assurance SeniorAssociate, you are responsible for the coordination and maintenance ofQuality Systems (i.e., Document Control, Record Control, TrainingProgram Maintenance, Deviation/CAPA, Complaints, Change Control) andprocesses to ensure internal and external compliance and the promotionof quality practices that meet or exceed required guidelines andregulatory requirements. The responsibilities include maintenance andcontinuous improvement of the overall Quality Program. Job dutiesinclude: Shift hours: Monday - Friday, 8:00am - 5:00pm Improvequality systems in ISO production environments. Controlleddocumentation activities involve managing the electronic documentationsystem, and the authority to write, review, or approve keydocuments(e.g., SOPs, Specifications, Manufacturing/Packaging Procedures). Training management involves coordinating activities, reporting metrics,and overseeing the electronic training platform to complete a highvolume of work and meet departmental goals. Communicate withcoworkers 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 maintaining site qualityand Life Science compliance, including participation in internal audits(and potentially serving as Lead Auditor), and supporting customercomplaint investigations. Contribute to Root Cause Investigations &Effectiveness Checks of Nonconforming Incidents. Conduct QualitySystem Training specific to job function. This individual will workwith various internal departments to develop, improve, and executeprocesses used in an ISO 9001 and ISO 13485 quality system environment.Who You Are Minimum Qualifications: Bachelor's Degree in Chemistry,Biology, Quality Engineering, or other scientific discipline OR HighSchool Diploma or GED with 4 + years prior experience working a QualityAssurance role Preferred Qualifications: Strong computer skills,including proficiency in MS Office (Word, Excel, Access, Project,PowerPoint) and competence in learning specific application software(e.g., SAP, Trackwise). Expertise in ISO 9001 and ISO 13485 andknowledge of global regulatorycompliance (e.g., FDA, IVDR, ICH, EDQM)for biologic materials in a controlled/regulated environment, with apreference for current fine chemical industry experience. Possessstrong verbal and written communication, customer service, andproblem-solving skills, with experience writing procedures and reports. Proficiency managing multiple tasks/priorities simultaneously Goodtime management and negotiating skills Proven capacity forindependent decision-making and task execution Pay Range for thisposition: $2 To view the full job description please use the linkbelow.y5jb20 APPLICATION INSTRUCTIONS: Apply Online:

Created: 2026-01-30