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Sr. Quality Assurance Associate

Merck Gruppe

Sheboygan Falls (WI)

Hybrid

USD 60,000 - 80,000

Full time

3 days ago
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Job summary

A leading company in life sciences is seeking a Sr. Quality Assurance Associate in Sheboygan Falls, WI. This hybrid role involves managing Change Management Quality systems, supporting compliance initiatives, and ensuring alignment with industry regulations. The ideal candidate has a strong foundation in quality assurance methodologies and excellent coordination skills.

Qualifications

  • Bachelor's degree in a relevant field or equivalent experience.
  • 2+ years in an industrial, manufacturing, or production environment.
  • Understanding of Quality System Regulations and ISO standards.

Responsibilities

  • Develop and maintain Change Management Quality systems.
  • Coordinate Change processes using TrackWise.
  • Conduct Employee Training in quality systems.

Skills

Knowledge of life sciences
Excellent verbal and written communication skills
Strong computer skills

Education

Bachelor's Degree in Chemistry, Biology, Healthcare, or another Life Science discipline
High School Diploma or GED with 2+ years of experience

Tools

MS Office Suite
Google applications
ERP systems

Job description

Work Location: Sheboygan Falls, Wisconsin
Shift: No
Department: LS-SC-PMSQA Sheboygan QA
Recruiter: Michelle Cole


This information is for internal use only. Please do not share outside of the organization.


Your Role

The Sr. Quality Assurance Associate at MilliporeSigma in Sheboygan Falls, WI, will serve as a TrackWise Change Coordinator, supporting quality systems and ensuring their alignment with business goals, customer expectations, and global best practices. The Associate will establish collaborative relationships across departments and will be responsible for delivering results within deadlines independently.

  • Develop and maintain Change Management Quality systems
  • Coordinate Genesis and TrackWise Change processes
  • Generate reports for internal and external customers
  • Manage Document Control
  • Conduct Employee Training
  • Work schedule: Monday – Friday, 7:00 AM – 3:30 PM. This is a hybrid role requiring on-site presence 2-3 days a week, with potential for full-time hours based on project needs.

Physical Attributes:

  • View computer monitors for extended periods
  • Sit, stand, and walk for extended periods
  • Use of phones, computers, monitors, and laboratory/office equipment

Who You Are

Minimum Qualifications:

  • Bachelor's Degree in Chemistry, Biology, Healthcare, or another Life Science discipline

OR

  • High School Diploma or GED with 2+ years of experience in an industrial, manufacturing, or production environment

Preferred Qualifications:

  • Knowledge of life sciences, chemicals, electronics, or healthcare industries
  • Excellent verbal and written communication skills
  • Understanding of Quality System Regulations, ISO standards, and FDA regulations
  • Strong computer skills, including MS Office Suite, Google applications, and ERP systems


The company is an Equal Employment Opportunity employer. Discrimination based on race, color, religion, age, sex, sexual orientation, national origin, disability, veteran status, or any other protected class is strictly prohibited. Concerns about discrimination should be reported immediately to HR, Legal, or Compliance. The company ensures no retaliation against individuals reporting discrimination in good faith.

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