Validation Engineer I

Posted 24 Mar 2020

St. Louis, Missouri - United States

Req Id 204790


A career with MilliporeSigma is an ongoing journey of discovery: our 56,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. 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:

In the role of Validation Engineer, incumbent will be interacting cross-functionally with Manufacturing, Project Management, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance to insure successful implementation and coordination of validation activities. Reporting to the Validation Supervisor, The Validation Engineer I position is responsible for developing, reviewing, and managing the execution of validation activities, and ensuring that the qualifications are consistent with user's/manufacturer's requirements and quality standards. Create and execute protocols for equipment, analytical instrumentation, cleaning, process controls, and facility (including but not limited to FAT/SAT/IOQ and PQ documents). Utilize GDP in a GMP atmosphere while generating protocols and reviewing documents. Review and generate closing reports for executed protocols. Create validation schedules, coordinate execution efforts with contractors, production operators, production engineers, customers and quality assurance staff members. Ability to work through a Management of Change system to determine the impact of proposed changes to the qualification status of equipment, software, or facilities. Sound understanding of Quality Risk Management concepts.


Physical Aspects:

  • This position may require rare lifting of no more than 35lbs.


Who you are:

Minimum Qualifications:

  • Bachelor's or Associates degree in an Engineering, Life Sciences discipline, or technical engineering science.
  • 1+ years quality or quality support experience in a cGMP pharmaceutical setting
  • Up to 6 months experience working with or awareness of pharmaceutical standards, rules and guidance (e.g. FDA, EU, ISO, ISPE, etc.)


Preferred Qualifications:

  • 2+ years facility, equipment, and/or cleaning validation experience in a cGMP manufacturing setting
  • Ability to utilize GDP during document creation and review
  • Comfortable in a fast-paced environment with the ability to adjust to changing priorities
  • Flexible and accountable



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

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.





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