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Software Validation Engineer

 

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. 

 

Your Role:

 

As a Software Validation Engineer at MilliporeSigma, you will guide and direct validation projects for all Life Science digital products, applications, and computerized systems. You will serve as a subject matter expert, providing leadership on computerized systems validation, quality governance, and regulatory compliance, including travel for critical site support during inspections or major projects. Responsibilities include the following:

 

  • Lead the qualification and validation of diverse digital products, computerized systems, and software solutions, including Control Systems, Cloud-based solutions, and Operational Technology (OT)
  • Execute the full validation lifecycle (IQ, OQ, PQ, protocols, test scripts, infrastructure qualification, backup/restoration, and audit trail testing) in both GMP and Non-GMP environments
  • Ensure compliance with global regulatory guidelines including GAMP, QMS, 21 CFR Part 11, and Annex 11
  • Perform critical assessments (Risk, Functional Risk, Data Integrity, FMEA) to define requirements and controls prior to development and verify tested systems meet those standards
  • Review and approve validation documentation, including URS, Functional/Design Specifications, and Test Scripts for COTS and new products
  • Develop and manage core validation documents, such as Test Scripts/Protocols, Test Summary Reports, Traceability Matrices, and Validation Summary Reports
  • Manage quality system activities, including Operational Change Control, Deviation/CAPA management, customer complaint handling, and periodic review/re-validation
  • Act as the validation expert during audits, effectively presenting and explaining qualification documents and reports to regulatory agencies, internal/external auditors, and customers
  • This is a hybrid role including 3 days on-site and 2 days remote work

 

Who You Are

 

Minimum Qualifications:

 

  • Bachelor’s degree in Chemistry, Chemical Engineering, Computer Science, Biomedical engineering or other Life Science discipline
  • 5+ years of experience in software and/or computerized validation 

 

Preferred Qualifications:

 

  • Excellent written and verbal skills
  • Prior automation testing experience
  • Excellent computer skills and experience in Project Planning, Word, Excel, PowerPoint, SharePoint
  • Qualified systems and supported process validation, ensuring compliance with GMP, GCP, GLP, GAMP, and Part 11 regulations
  • Global travel based on the need of project and business

RSREMD

Salary range for this position - $66,800.00 - $109,300.00 annually

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. 

 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

 

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job Requisition ID:  293641
Location:  St. Louis
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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