Senior QA Associate
MilliporeSigma

Madison, Wisconsin

Posted in Science and Research


This job has expired.

Job Info


A career with MilliporeSigma is an ongoing journey of discovery: our 57,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.

Your Role:

Quality Assurance operations representation possesses detailed knowledge of document control. Highly developed interpersonal and verbal skills with attention to detail. They must be able to establish a strong collaborative relationship with all departments within the organization to deliver on quality and regulatory commitments and have the ability to work autonomously, effectively manage time and deliver results on time

  • Management and overview Of the Document system. QAO ensures that all documentation is issued, managed, and controlled using a document management system and in compliance with GMP. QAO are subject matter experts on Mango, SAP, and other data systems.
  • Document approval and distribution. QAO is responsible for adequacy and approval prior to issuance of all documents and ensuring that documents shall be available at all locations for which they are designated, used, or otherwise necessary, and all obsolete documents shall be promptly removed from all points of use or otherwise prevented from unintended use.
  • Document changes. Changes to documents shall be reviewed and approved.
  • Archiving and storage QAO is also responsible for the storage of all GMP documentation and all forms of data.

Who You Are:

Minimum qualifications:
  • BS degree in Chemistry, Biology, Quality Assurance, or related discipline
  • 1+ year quality experience working in a cGMP or CMO environment

Preferred Qualifications:
  • Ability to prioritize, manage time well, work independently and be task-oriented.
  • Strong interpersonal, communication, and customer service skills.
  • Computer skills with systems such as Microsoft Office and others as needed.
  • General understanding of cGMP, ICH Q7, and Good Documentation Practices
  • Experience with personal computer software in a business environment, including word processing, database, spreadsheet and draw programs.
  • Microsoft Office

What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

Curious? Apply and find more information at https://jobs.vibrantm.com

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.

Job Requisition ID: 218376

Location: Madison

Career Level: C - Professional (1-3 years)

Working time model: full-time


This job has expired.

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