Sr. Quality Assurance Associate
Millipore Corporation

Sheboygan Falls, Wisconsin

Posted in Science and Research


This job has expired.

Job Info


Work Location: Sheboygan Falls, Wisconsin
Shift:
Department: LS-SC-PMSQA2 Sheboygan QA2
Recruiter: Michelle Cole

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

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

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.


This job has expired.

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